2023

Koens, L.H., Klamer, M.R., Sival, D.A., Balint, B., Bhatia, K.P., Contarino, M.F., ...Fung, V.S.C. (2023). A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism. Movement Disorders, doi:10.1002/mds.29332
Rajapakshe, I., Mulroy, E., Magrinelli, F., Makawita, C., Bhatia, K.P., Senanayake, B. (2023). Cranial dystonia as an isolated presentation of DJ-1 disease: Case report and literature review. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13591
Mancuso, M., Graessner, H., de Visser, M., Arsovska, A., Bhatia, K. (2023). Key priorities in rare neurological diseases: A statement from the Coordinating Panel on Rare Neurological Diseases of the European Academy of Neurology.. European Journal of Neurology, doi:10.1111/ene.15752
Foltynie, T., Gandhi, S., Gonzalez-Robles, C., Zeissler, M.-.L., Mills, G., Barker, R., ...Bandmann, O. (2023). Towards a multi-arm multi-stage platform trial of disease modifying approaches in Parkinson's disease. Brain, awad063. doi:10.1093/brain/awad063

2022

Sadnicka, A., Rocchi, L., Latorre, A., Antelmi, E., Teo, J., Pareés, I., ...Edwards, M.J. (2022). A Critical Investigation of Cerebellar Associative Learning in Isolated Dystonia. Movement Disorders, doi:10.1002/mds.28967
Huys, A.M.L., Haggard, P., Bhatia, K.P., Edwards, M.J. (2022). A Note of Caution on Distorted Visual Feedback as a Treatment for Functional Movement Disorders. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13386
Koya Kutty, S., Magrinelli, F., Milner, A.V., Bhatia, K.P. (2022). Abnormal DaTscan in GM1-gangliosidosis type III manifesting with dystonia-parkinsonism. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13512
Thust, S., Veneziano, L., Parkinson, M.H., Bhatia, K.P., Mantuano, E., Gonzalez-Robles, C., ...Giunti, P. (2022). Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations. Neurogenetics, doi:10.1007/s10048-021-00680-3
Magrinelli, F., Cali, E., Braga, V.L., Yis, U., Tomoum, H., Shamseldin, H., ...Povoas Barsottini, O.G. (2022). Biallelic Loss-of-Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13398
Christensen, M.B., Levy, A.M., Mohammadi, N.A., Niceta, M., Kaiyrzhanov, R., Dentici, M.L., ...Bhatia, K.P. (2022). Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.. Clinical Genetics, doi:10.1111/cge.14165
Dressler, D., Rothwell, J.C., Bhatia, K., Kopp, B., Bigalke, H., Adib Saberi, F. (2022). Botulinum toxin antibody titres: measurement, interpretation, and practical recommendations. Journal of Neurology, doi:10.1007/s00415-022-11424-0
Malaquias, M.J., Magrinelli, F., Bhatia, K.P. (2022). Breakthrough news in adenoviral vector-mediated AADC gene therapy: Lessons from the success in AADC deficiency and possible future applications. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13503
Schreglmann, S.R., Burke, D., Batla, A., Kresojevic, N., Wood, N., Heales, S., Bhatia, K.P. (2022). Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia.. Movement Disorders, doi:10.1002/mds.28937
Magrinelli, F., Bhatia, K.P., Beiraghi Toosi, M., Arab, F., Karimiani, E.G., Sedighzadeh, S., ...Houlden, H. (2022). Childhood-onset choreo-dystonia due to a recurrent novel homozygous nonsense HPCAvariant: case series and literature review. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13529
Zeissler, M.L., Allison, J., Athauda, D., Pires, S.B., Baxendale, G., Bhatia, K., ...Croucher, R. (2022). Designing a multi-arm multi-stage trial for Parkinson's.
Magrinelli, F., Rocca, C., Simone, R., Zenezini Chiozzi, R., Jaunmuktane, Z., Mencacci, N.E., ...Demidov, G. (2022). Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2-1-Related Disorder. Movement Disorders, doi:10.1002/mds.29280
Zeissler, M.L., Allison, J., Athauda, D., Pires, S.B., Baxendale, G., Bhatia, K., ...Croucher, R. (2022). Developing infrastructure for a multi-arm multi-stage trial in Parkinson's.
Benson, M., Albanese, A., Bhatia, K., Cavillon, P., Cuffe, L., Konig, K., ...Graessner, H. (2022). Development of a patient journey map for people living with cervical dystoni.
Benson, M., Albanese, A., Bhatia, K.P., Cavillon, P., Cuffe, L., Koenig, K., ...Graessner, H. (2022). Development of a patient journey map for people living with cervical dystonia. Orphanet Journal of Rare Diseases, 17 (1), doi:10.1186/s13023-022-02270-4
Vichayanrat, E., Valerio, F., Koay, S., De Pablo-Fernandez, E., Panicker, J., Morris, H., ...Quinn, N. (2022). Diagnosing Premotor Multiple System Atrophy: Natural History and Autonomic Testing in an Autopsy Confirmed Cohort.. Neurology, doi:10.1212/WNL.0000000000200861
Haering, V., Selzam, V., Peach, R., Martin-Rodriguez, J., Schwingenschuh, P., Tamas, G., ...Volkmann, J. (2022). Differentiation of Essential and Parkinson's Disease Tremor using time series feature extraction and machine learning.
Zago, E., Dal Molin, A., Dimitri, G.M., Xumerle, L., Pirazzini, C., Bacalini, M.G., ...Gómez-Garre, P. (2022). Early downregulation of hsa-miR-144-3p in serum from drug-naïve Parkinson’s disease patients. Scientific Reports, 12 doi:10.1038/s41598-022-05227-6
Merello, M., Bhatia, K. (2022). Editors Note: Looking Forward, Looking Back. MOVEMENT DISORDERS CLINICAL PRACTICE, 10 (1), 6. doi:10.1002/mdc3.13629
Mulroy, E., Macerollo, A., Scotton, S., Cociasu, I., Di Lazzaro, G., Bashir, S., ...Batla, A. (2022). Ethnic Differences in Dystonia Prevalence and Phenotype. Movement Disorders, doi:10.1002/mds.29034
Cullinane, P.W., Sidle, K., Bhatia, K.P., Revesz, T., Warner, T.T. (2022). Globular glial tauopathy type II.. Practical Neurology, doi:10.1136/pn-2022-003549
Magrinelli, F., Moualek, D., Tazir, M., Ali Pacha, L., Verghese, A., Bhatia, K.P., ...Houlden, H. (2022). Heterozygous EIF2AK2 variant causes adolescence‐onset generalized dystonia partially responsive to DBS. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13371
Mulroy, E., Balint, B., Bhatia, K.P. (2022). Homer-3 Antibody Disease: A Potentially Treatable MSA-C Mimic. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13404
Schreglmann, S.R., Bhatia, K.P. (2022). HOPS ‐associated neurological disorders ‐ lysosomal dysfunction as an emerging concept underlying dystonia. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13405
Meoni, G., Tenori, L., Schade, S., Licari, C., Pirazzini, C., Bacalini, M.G., ...Bartoletti-Stella, A. (2022). Metabolite and lipoprotein profiles reveal sex-related oxidative stress imbalance in de novo drug-naive Parkinson's disease patients. npj Parkinson's Disease, 8 doi:10.1038/s41531-021-00274-8
Erro, R., Fasano, A., Barone, P., Bhatia, K.P. (2022). Milestones in Tremor Research: ten years later. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13418
Leodori, G., De Bartolo, M.I., Guerra, A., Fabbrini, A., Rocchi, L., Latorre, A., ...Bhatia, K.P. (2022). Motor Cortical Network Excitability in Parkinson's Disease. MOVEMENT DISORDERS, doi:10.1002/mds.28914
Huys, A.-.C.M.L., Haggard, P., Bhatia, K.P., Edwards, M.J. (2022). No exaggerated tremor severity perception in functional tremor.. Journal of Neurology, doi:10.1007/s00415-022-11265-x
Morales-Briceno, H., Fung, V.S.C., Bhatia, K.P., Balint, B. (2022). Parkinsonism and dystonia: Clinical spectrum and diagnostic clues.. Journal of Neurological Sciences, 120016. doi:10.1016/j.jns.2021.120016
Rajapakshe, I., Menozzi, E., Cunha, I., Lees, A.J., Bhatia, K.P., Mulroy, E. (2022). Patients’ post‐judice of tele‐neurology for movement disorders. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13434
Alshimemeri, S., Di Luca, D.G., Olszewska, D.A., Mulroy, E., Bhatia, K.P., Fox, S.H., Lang, A.E. (2022). Periodic Limb Movements While Awake (PLMA) as a manifestation of Wearing‐Off in Parkinson's Disease: A Case Series and Review of the Literature. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13487
Lang, A.E., Bhatia, K.P. (2022). Preface to the 2021 Video Challenge Supplement for Movement Disorders Clinical Practice. MOVEMENT DISORDERS CLINICAL PRACTICE, 9 S5. doi:10.1002/mdc3.13543
Malaquias, M.J., Magrinelli, F., Quattrone, A., Neo, R.J., Latorre, A., Mulroy, E., Bhatia, K.P. (2022). Presynaptic hemiparkinsonism following cerebral toxoplasmosis: case report and literature review. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13631
Rajapakshe, I., Menozzi, E., Cunha, I., Lees, A.J., Bhatia, K.P., Mulroy, E. (2022). Reply to Comment on "Patients' Postjudice of Tele‐Neurology for Movement Disorders. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13548
Magrinelli, F., Rajapaksha, I., Kobylecki, C., Latorre, A., Mulroy, E., Estevez-Fraga, C., ...Bhatia, K.P. (2022). Reply to: Juvenile PLA2G6-parkinsonism due to Indian 'Asian' p.R741Q mutation, and response to STN DBS.. Movement Disorders, doi:10.1002/mds.28955
Antelmi, E., Rocchi, L., Latorre, A., Belvisi, D., Magrinelli, F., Bhatia, K.P., Tinazzi, M. (2022). Restless Legs Syndrome: Known Knowns and Known Unknowns. Brain Sciences, 12 (1), doi:10.3390/brainsci12010118
Latorre, A., Hallett, M., Deuschl, G., Bhatia, K.P. (2022). The MDS consensus tremor classification: The best way to classify patients with tremor at present.. Journal of the Neurological Sciences, 435 120191. doi:10.1016/j.jns.2022.120191
Bhatia, K. (2022). The translational clinician: big gains from small observations.
Selzam, V., Haering, V., Peach, R., Martin-Rodriguez, J., Schwingenschuh, P., Mir, P., ...Schreglmann, S. (2022). Unbiased phenotypical characterization of Essential and Dystonic tremor using time-series feature analysis.

2021

Balint, B., Bhatia, K.P., Dalmau, J. (2021). "Antibody of Unknown Significance" (AUS): The Issue of Interpreting Antibody Test Results.. Movement Disorders, doi:10.1002/mds.28597
Mulroy, E., Vijiaratnam, N., De Roquemaurel, A., Bhatia, K.P., Zrinzo, L., Foltynie, T., Limousin, P. (2021). A practical guide to troubleshooting pallidal deep brain stimulation issues in patients with dystonia.. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2021.05.017
Balint, B., Bhatia, K.P. (2021). Autoimmune movement disorders with neuronal antibodies - an update.. Current Opinion in Neurology, doi:10.1097/WCO.0000000000000956
Mencacci, N.E., Brockmann, M.M., Dai, J., Pajusalu, S., Atasu, B., Campos, J., ...Schwake, M. (2021). Bi-allelic variants in TSPOAP1, encoding the active zone protein RIMBP1, cause autosomal recessive dystonia.. J Clin Invest, doi:10.1172/JCI140625
Magrinelli, F., Balint, B., Bhatia, K.P. (2021). Challenges in clinicogenetic correlations: One gene – many phenotypes unravelling the basis of phenotypic heterogeneity in monogenic disorders. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13165
Bhatia, K.P., Cociasu, I., Sorbera, C., Tuttolomondo, A., Morgante, F., Friedman, J. (2021). Commentary: Anderson‐Fabry Disease: A Rare Cause of Levodopa‐Responsive Early Onset Parkinsonism. Movement Disorders Clinical Practice, 8 (S1), doi:10.1002/mdc3.13297
Latorre, A., Rocchi, L., Cocco, A., Erro, R., Antelmi, E., Conte, A., ...Bhatia, K. (2021). Defective somatosensory inhibition and plasticity are not required to develop dystonia.
Balint, B., Mulroy, E., Gövert, F., Latorre, A., Di Lazarro, G., Erro, R., ...Warner, T.T. (2021). Development of parkinsonism after long-standing cervical dystonia - A cohort. Journal of the Neurological Sciences, 427 117477. doi:10.1016/j.jns.2021.117477
Magrinelli, F., Mehta, S., Di Lazzaro, G., Latorre, A., Edwards, M.J., Balint, B., ...Hegde, A. (2021). Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism. Movement Disorders, doi:10.1002/mds.28807
Calandra-Buonaura, G., Alfonsi, E., Vignatelli, L., Benarroch, E.E., Giannini, G., Iranzo, A., ...Quinn, N. (2021). Dysphagia in multiple system atrophy consensus statement on diagnosis, prognosis and treatment.. Parkinsonism Relat Disord, doi:10.1016/j.parkreldis.2021.03.027
Mencacci, N.E., Reynolds, R., Ruiz, S.G., Vandrovcova, J., Forabosco, P., Sanchez-Ferrer, A., ...Webber, C. (2021). Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders (vol 143, pg 2771, 2020). BRAIN, 144 doi:10.1093/brain/awaa366
Ros‐Castelló, V., Latorre, A., Álvarez‐Linera, J., Martinez‐Castrillo, J.C., Bhatia, K.P., Pareés, I. (2021). Dystonia in a female fragile X premutation carrier: a case report. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13234
Estevez-Fraga, C., Magrinelli, F., Hensman Moss, D., Mulroy, E., Di Lazzaro, G., Latorre, A., ...Bhatia, K.P. (2021). Expanding the Spectrum of Movement Disorders Associated With C9orf72 Hexanucleotide Expansions. Neurology Genetics, 7 (2), e575. doi:10.1212/nxg.0000000000000575
Batla, A., Simeoni, S., Uchiyama, T., deMin, L., Baldwin, J., Melbourne, C., ...Eriksson, S. (2021). Exploratory pilot study of exogenous sustained-release Melatonin on nocturia in Parkinson's Disease.. European Journal of Neurology, doi:10.1111/ene.14774
Becktepe, J., Gövert, F., Balint, B., Schlenstedt, C., Bhatia, K., Elble, R., Deuschl, G. (2021). Exploring interrater disagreement on essential tremor using a standardized tremor elements assessment. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13150
Latorre, A., Rocchi, L., Manzo, N., Rothwell, J., Bhatia, K. (2021). Exploring the usefulness of Repetitive Transcranial Magnetic Stimulation for treatment of pain and fatigue in Parkinson's disease.
Colucci, F., Carvalho, V., Gonzalez‐Robles, C., Bhatia, K.P., Mulroy, E. (2021). From Collar to Coccyx: Truncal Movement Disorders: A Clinical Review. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13325
Baldelli, L., Schade, S., Jesús, S., Schreglmann, S.R., Sambati, L., Gómez-Garre, P., ...Sixel-Döring, F. (2021). Heterogeneity of prodromal Parkinson symptoms in siblings of Parkinson disease patients. npj Parkinson's Disease, 7 doi:10.1038/s41531-021-00219-1
Koya Kutty, S., Mulroy, E., Magrinelli, F., Di Lazzaro, G., Latorre, A., Bhatia, K.P. (2021). Huntington disease-like phenotype in a patient with ANO3 mutation. Parkinsonism Relat Disord, doi:10.1016/j.parkreldis.2021.02.022
Dursun, N., Chung, T.M., Colosimo, C., Bhidayasiri, R., Bhatia, K., Tiley, J., Jacinto, L.J. (2021). IMPROVEMENT OF SPASTIC PARESIS AND CERVICAL DYSTONIA MANAGEMENT: ASSESSMENT OF SEVEN YEARS OF THE INNOVATIVE INTERNATIONAL EDUCATIONAL PROGRAM IXCELLENCE NETWORK (R).
Shahedah, K.K., Di Lazzaro, G., Magrinelli, F., Mulroy, E., Latorre, A., Bhatia, K.P. (2021). Late‐onset chorea in JAK2‐associated essential thrombocythemia. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13105
Tucker, H., Osei‐Poku, F., Ashton, D., Lally, R., Jesuthasan, A., Latorre, A., ...Kobylecki, C. (2021). Management of secondary poor response to botulinum toxin in cervical dystonia: a multicentre audit. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13181
Huys, A.-.C.M.L., Haggard, P., Bhatia, K.P., Edwards, M.J. (2021). Misdirected attentional focus in functional tremor. Brain, doi:10.1093/brain/awab230
Leodori, G., De Bartolo, M.I., Guerra, A., Fabbrini, A., Belvisi, D., Paparella, G., ...Rothwell, J. (2021). Motor cortical network excitability in Parkinson's disease: A transcranial magnetic stimulation-electroencephalography study.
Mulroy, E., Baschieri, F., Magrinelli, F., Latorre, A., Cortelli, P., Bhatia, K.P. (2021). Movement Disorders and Liver Disease. Movement Disorders Clinical Practice, 8 (6), 828-842. doi:10.1002/mdc3.13238
Menozzi, E., Mulroy, E., Akbarian-Tefaghi, L., Bhatia, K.P., Balint, B. (2021). Movement disorders in systemic autoimmune diseases: Clinical spectrum, ancillary investigations, pathophysiological considerations.. Parkinsonism Relat Disord, doi:10.1016/j.parkreldis.2021.05.026
Huys, A.-.C.M.L., Beck, B., Haggard, P., Bhatia, K.P., Edwards, M.J. (2021). No Increased Suggestibility to Placebo in Functional Neurological Disorder. European Journal of Neurology, doi:10.1111/ene.14816
Di Lazzaro, G., Mulroy, E., Frezza, E., Massa, R., Pisani, A., Bhatia, K. (2021). Non-dopaminergic freezing.
Schreglmann, S.R., Wang, D., Peach, R.L., Li, J., Zhang, X., Latorre, A., ...Boyden, E.S. (2021). Non-invasive suppression of essential tremor via phase-locked disruption of its temporal coherence. Nature Communications, 12 (1), doi:10.1038/s41467-020-20581-7
Mulroy, E., Magrinelli, F., Mohd Fauzi, N.A., Kutty, S.K., Latorre, A., Bhatia, K.P. (2021). Paroxysmal, exercise-induced, diurnally fluctuating dystonia: Expanding the phenotype of SPG8.. Parkinsonism Relat Disord, 85 26-28. doi:10.1016/j.parkreldis.2021.02.011
Bhatia, K. (2021). Phenotypes-genotypes in dystonia.
Sadnicka, A., Dennis, E., Rothwell, J., Bhatia, K., Chen, X., Galea, J. (2021). Postural instability in DYT-TOR1A dynamically dependent on sensory state.
Bonomo, R., Latorre, A., Bhatia, K.P. (2021). Reply to Comment on: Voluntary Inhibitory Control of Chorea. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13189
Latorre, A., Rocchi, L., Batla, A., Berardelli, A., Rothwell, J.C., Bhatia, K.P. (2021). Reply to: "A Primary Writing Tremor Is a Form of Dystonic Tremor: Is the Debate Settled?". MOVEMENT DISORDERS, 36 (8), 1996-1997. doi:10.1002/mds.28695
Balint, B., Bhatia, K.P., Dalmau, J. (2021). Reply to: Comparing VUS and AUS: Parallels and Differences in Neurogenetics and Neuroimmunology. MOVEMENT DISORDERS, 36 (10), 2454-2456. doi:10.1002/mds.28764
Merello, M., Bhatia, K.P., Obeso, J.A. (2021). SARS-CoV-2 and the risk of Parkinson's disease: facts and fantasy. The Lancet Neurology, 20 (2), 94-95. doi:10.1016/S1474-4422(20)30442-7
Mulroy, E., Ganos, C., Latorre, A., Terkelsen, A.J., Balint, B., Agarwal, P.A., ...Bhatia, K.P. (2021). Self-concocted, curious and creative coping strategies in movement disorders. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2020.10.031
Merello, M., Bhatia, K.P. (2021). Standing on the Shoulders of Giants: The Most Relevant Papers in Movement Disorders Field from the Second Half of the 20th Century. MOVEMENT DISORDERS CLINICAL PRACTICE, 8 (7), 992. doi:10.1002/mdc3.13335
Huys, A.M.L., Bhatia, K.P., Haggard, P., Edwards, M.J. (2021). Symptom‐triggered Attention to Self as a Possible Trigger of Functional Comorbidity. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13120
Erro, R., Mencacci, N.E., Bhatia, K.P. (2021). The Emerging Role of Phosphodiesterases in Movement Disorders. Movement Disorders, doi:10.1002/mds.28686
Sadnicka, A., Rocchi, L., Latorre, A., Antelmi, E., Teo, J., Pareés, I., ...Edwards, M. (2021). The final blink: intact eyeblink conditioning in isolated dystonia. .
Ganos, C., Neumann, W.J., Müeller-Vahl, K.R., Bhatia, K.P., Hallett, M., Haggard, P., Rothwell, J. (2021). The Phenomenon of Exquisite Motor Control in Tic Disorders and its Pathophysiological Implications. Movement Disorders, doi:10.1002/mds.28557
Latorre, A., Rocchi, L., Batla, A., Berardelli, A., Rothwell, J.C., Bhatia, K.P. (2021). The Signature of Primary Writing Tremor Is Dystonic. MOVEMENT DISORDERS, doi:10.1002/mds.28579
Mulroy, E., Ilinca, A., Gonzalez‐Robles, C., Magrinelli, F., Puschmann, A., Bhatia, K.P. (2021). Throat-Clearing Vocalizations in Primary Brain Calcification Syndromes. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13175
Fong, P.Y., Spampinato, D., Rocchi, L., Hannah, R., Teng, Y., Di Santo, A., ...Rothwell, J.C. (2021). Two forms of short-interval intracortical inhibition in human motor cortex. Brain Stimulation, 14 (5), 1340-1352. doi:10.1016/j.brs.2021.08.022
Gatto, E.M., Walker, R.H., Gonzalez, C., Cesarini, M., Cossu, G., Stephen, C.D., ...Morgante, F. (2021). Worldwide barriers to genetic testing for movement disorders. European Journal of Neurology, doi:10.1111/ene.14826
Di Lazzaro, G., Magrinelli, F., Estevez-Fraga, C., Valente, E.M., Pisani, A., Bhatia, K.P. (2021). X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.. Movement Disorders, doi:10.1002/mds.28565

2020

Pirazzini, C., Azevedo, T., Baldelli, L., Bartoletti-Stella, A., Calandra-Buonaura, G., Molin, A.D., ...Hägg, S. (2020). A Geroscience approach for Parkinson's Disease: conceptual framework and design of PROPAG-AGEING project.. Mech Ageing Dev, 111426. doi:10.1016/j.mad.2020.111426
Estevez-Fraga, C., Magrinelli, F., Latorre, A., Cordivari, C., Houlden, H., Tinazzi, M., ...Bhatia, K.P. (2020). A new family with GLRB-related hyperekplexia showing chorea in homo- and heterozygous variant carriers. Parkinsonism and Related Disorders, 79 97-99. doi:10.1016/j.parkreldis.2020.08.016
Gövert, F., Leypoldt, F., Junker, R., Wandinger, K.-.P., Deuschl, G., Bhatia, K.P., Balint, B. (2020). Antibody-related movement disorders - a comprehensive review of phenotype-autoantibody correlations and a guide to testing.. Neurol Res Pract, 2 6. doi:10.1186/s42466-020-0053-x
Andelman-Gur, M.M., Leventer, R.J., Hujirat, M., Ganos, C., Yosovich, K., Carmi, N., ...Bhatia, K. (2020). Bilateral polymicrogyria associated with dystonia: A new neurogenetic syndrome?. American Journal of Medical Genetics, Part A, doi:10.1002/ajmg.a.61795
Chung, T.M., Jacinto, L.J., Colosimo, C., Bhatia, K.P., Tiley, J., Bhidayasiri, R. (2020). Botulinum Neurotoxin-A Injection in Adult Cervical Dystonia and Spastic Paresis: Results From the INPUT (INjection Practice, Usage and Training) Survey. Frontiers in Neurology, 11 doi:10.3389/fneur.2020.570671
Magrinelli, F., Mulroy, E., Schneider, S.A., Latorre, A., Di Lazzaro, G., Hennig, A., ...Bhatia, K.P. (2020). Criss-cross gait: A clue to glucose transporter type 1 deficiency syndrome. Neurology, doi:10.1212/WNL.0000000000010502
Latorre, A., Cocco, A., Bhatia, K.P., Erro, R., Antelmi, E., Conte, A., ...Rocchi, L. (2020). Defective Somatosensory Inhibition and Plasticity Are Not Required to Develop Dystonia. MOVEMENT DISORDERS, doi:10.1002/mds.28427
Latorre, A., Rocchi, L., Bhatia, K.P. (2020). Delineating the electrophysiological signature of dystonia. Experimental Brain Research, doi:10.1007/s00221-020-05863-2
Mencacci, N.E., Reynolds, R., Ruiz, S.G., Vandrovcova, J., Forabosco, P., Sánchez-Ferrer, A., ...Weale, M.E. (2020). Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders.. Brain, doi:10.1093/brain/awaa217
Latorre, A., Rocchi, L., Rothwell, J., Bhatia, K. (2020). Exploring the pathophysiology of acquired dystonia by the use of high frequency somatosensory stimulation.
Mencacci, N., Brockmann, M., Pajusalu, S., Atasu, B., Latapi, P.G., Schwake, M., ...Simon-Sanchez, J. (2020). Homozygous BZRAP1 Mutations Cause Autosomal Recessive Dystonia.
Mulroy, E., Latorre, A., Menozzi, E., Teh, P.C., Magrinelli, F., Bhatia, K.P. (2020). Huntington disease like 2 (HDL-2) with parkinsonism and abnormal DAT-SPECT – A novel observation. Parkinsonism and Related Disorders, 71 46-48. doi:10.1016/j.parkreldis.2020.01.008
Rawji, V., Modi, S., Latorre, A., Rocchi, L., Hockey, L., Bhatia, K., ...Jahanshahi, M. (2020). Impaired automatic but intact volitional inhibition in primary tic disorders. Brain, doi:10.1093/brain/awaa024
Magrinelli, F., Latorre, A., Balint, B., Mackenzie, M., Mulroy, E., Stamelou, M., ...Bhatia, K.P. (2020). Isolated and combined genetic tremor syndromes: a critical appraisal based on the 2018 MDS criteria. Parkinsonism and Related Disorders, 77 121-140. doi:10.1016/j.parkreldis.2020.04.010
Balint, B., Guerreiro, R., Carmona, S., Dehghani, N., Latorre, A., Cordivari, C., ...Bras, J. (2020). KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia. European Journal of Neurology, doi:10.1111/ene.14228
Cif, L., Demailly, D., Lin, J.-.P., Barwick, K.E., Sa, M., Abela, L., ...Sanchis-Juan, A. (2020). KMT2B-related disorders: expansion of the phenotypic spectrum and long-term efficacy of deep brain stimulation.. Brain, doi:10.1093/brain/awaa304
Relja, M., Miletic, V., Albanese, A., Bhatia, K., Dressler, D., Ferreira, J., ...Vidailhet, M. (2020). Management and Quality of Life of Dystonia Patients in Europe: A Survey Towards Care from a Patients' Experience.
Huys, A.C.M.L., Edwards, M.J., Bhatia, K.P., Haggard, P. (2020). Modulation of Reaction Times and Sense of Agency via Subliminal Priming in Functional Movement Disorders. Frontiers in Neurology, 11 doi:10.3389/fneur.2020.00989
Stoessl, A.J., Bhatia, K.P., Merello, M. (2020). Movement Disorders in the World of COVID‐19. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12952
Stoessl, A.J., Bhatia, K.P., Merello, M. (2020). Movement Disorders in the World of COVID-19.. Mov Disord, doi:10.1002/mds.28069
Chelban, V., Carecchio, M., Rea, G., Bowirrat, A., Kirmani, S., Magistrelli, L., ...Salpietro, V. (2020). MYORG-related disease is associated with central pontine calcifications and atypical parkinsonism.. Neurol Genet, 6 (2), e399. doi:10.1212/NXG.0000000000000399
Vokurka, P., Barron, A., Sumaria, S., Stockford, L., Jarman, P., Bhatia, K., ...Weil, R. (2020). Opicapone Efficacy and Tolerability in Parkinson's Disease Patients Reporting Insufficient Benefit/Failure of Entacapone. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13094
Balint, B., Damasio, J., Magrinelli, F., Guerreiro, R., Bras, J., Bhatia, K.P. (2020). Psychiatric manifestations of ATP13A2 mutations. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13034
Berlot, R., Bhatia, K.P., Kojović, M. (2020). Reply to J. Dulski and J. Slawek's “Fibrodysplasia ossificans progressiva as a form of pseudodystonia”. Parkinsonism and Related Disorders, 71 49-50. doi:10.1016/j.parkreldis.2020.01.016
Mulroy, E., Menozzi, E., Lees, A.J., Lynch, T., Lang, A.E., Bhatia, K.P. (2020). Reply to: A New Day: The Role of Telemedicine in Reshaping Care for Persons with Movement Disorders. Movement Disorders, doi:10.1002/mds.28315
Latorre, A., Rocchi, L., Magrinelli, F., Mulroy, E., Berardelli, A., Rothwell, J.C., Bhatia, K.P. (2020). Reply: Pentameric repeat expansions: cortical myoclonus or cortical tremor? and Cortical tremor: a tantalizing conundrum between cortex and cerebellum. BRAIN, 143 E88-+. doi:10.1093/brain/awaa261
Erro, R., Antelmi, E., Bhatia, K.P., Latorre, A., Tinazzi, M., Berardelli, A., ...Rocchi, L. (2020). Reversal of Temporal Discrimination in Cervical Dystonia after Low-Frequency Sensory Stimulation.. Mov Disord, doi:10.1002/mds.28369
Fischer, J.-.F., Mainka, T., Worbe, Y., Pringsheim, T., Bhatia, K., Ganos, C. (2020). Self-injurious behaviour in movement disorders: systematic review.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2019-322569
Mulroy, E., Jaunmuktane, Z., Balint, B., Erro, R., Latorre, A., Bhatia, K.P. (2020). Some new and unexpected tauopathies in movement disorders. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12995
Mulroy, E., Balint, B., Bhatia, K.P. (2020). Tardive syndromes.. Pract Neurol, doi:10.1136/practneurol-2020-002566
Mulroy, E., Menozzi, E., Lees, A.J., Lynch, T., Lang, A.E., Bhatia, K.P. (2020). Telemedicine in movement disorders – Leçons du COVID‐19. Movement Disorders, doi:10.1002/mds.28297
Jha, A., Menozzi, E., Oyekan, R., Latorre, A., Mulroy, E., Schreglmann, S.R., ...Luchini, M. (2020). The CloudUPDRS smartphone software in Parkinson's study: cross-validation against blinded human raters.. NPJ Parkinsons Dis, 6 (1), 36. doi:10.1038/s41531-020-00135-w
Huys, A.C.M.L., Bhatia, K.P., Edwards, M.J., Haggard, P. (2020). The Flip Side of Distractibility—Executive Dysfunction in Functional Movement Disorders. Frontiers in Neurology, 11 doi:10.3389/fneur.2020.00969
Di Lazzaro, G., Magrinelli, F., Ganos, C., Bhatia, K.P. (2020). The Need to Tic. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13023
Piot, I., Schweyer, K., Respondek, G., Stamelou, M., DescribePSP study, g.r.o.u.p., ProPSP study, g.r.o.u.p., ...Goetz, C.G. (2020). The Progressive Supranuclear Palsy Clinical Deficits Scale. Movement Disorders, doi:10.1002/mds.27964
Latorre, A., Rocchi, L., Bhatia, K. (2020). The role of the cerebellum in cortical myoclonus: a neurophysiological study.
Latorre, A., Rocchi, L., Paparella, G., Berardelli, A., Rothwell, J., Bhatia, K. (2020). The role of the cerebellum in cortical myoclonus: a neurophysiological study.
Magrinelli, F., Tinazzi, M., Bhatia, K.P. (2020). Toward an Early Real-Time Quaking-Induced Conversion–Based Diagnostic Biomarker for Lewy Body–Related Synucleinopathies. Movement Disorders Clinical Practice, doi:10.1002/mdc3.13050
Latorre, A., Bhatia, K.P. (2020). Treatment of Paroxysmal Dyskinesia. Neurologic Clinics, 38 (2), 433-447. doi:10.1016/j.ncl.2020.01.007
Latorre, A., Rocchi, L., Magrinelli, F., Mulroy, E., Berardelli, A., Rothwell, J.C., Bhatia, K.P. (2020). Unravelling the enigma of cortical tremor and other forms of cortical myoclonus. Brain, doi:10.1093/brain/awaa129
Berlot, R., Rothwell, J.C., Bhatia, K.P., Kojović, M. (2020). Variability of Movement Disorders: The Influence of Sensation, Action, Cognition, and Emotions. Movement Disorders, doi:10.1002/mds.28415
Iankova, V., Respondek, G., Saranza, G., Painous, C., Cámara, A., Compta, Y., ...Josephs, K.A. (2020). Video-tutorial for the Movement Disorder Society criteria for progressive supranuclear palsy. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2020.06.030
Bonomo, R., Latorre, A., Balint, B., Smilowska, K., Rocchi, L., Rothwell, J.C., ...Bhatia, K.P. (2020). Voluntary inhibitory control of chorea: a case series. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12907

2019

Rocchi, L., Latorre, A., Ibanez Pereda, J., Spampinato, D., Brown, K.E., Rothwell, J., Bhatia, K. (2019). A case of congenital hypoplasia of the left cerebellar hemisphere and ipsilateral cortical myoclonus. Movement Disorders, doi:10.1002/mds.27881
Merello, M., Bhatia, K. (2019). A New Year and a New Era for MDCP. Movement Disorders Clinical Practice, 6 (2), 95. doi:10.1002/mdc3.12731
Gultekin, M., Prakash, N., Ganos, C., Mirza, M., Bayramov, R., Bhatia, K.P., Mencacci, N.E. (2019). A Novel SGCE Nonsense Variant Associated With Marked Intrafamilial Variability in a Turkish Family With Myoclonus-Dystonia. Movement Disorders Clinical Practice, 6 (6), 479-482. doi:10.1002/mdc3.12805
Latorre, A., Del Gamba, C., Menozzi, E., Balint, B., Brugger, F., Bhatia, K.P. (2019). Abnormal DaTSCAN and Atypical Parkinsonism in SCA12. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12751
Vijiaratnam, N., Bhatia, K.P., Lang, A.E., Raskind, W.H., Espay, A.J. (2019). ADCY5–Related Dyskinesia: Improving Clinical Detection of an Evolving Disorder. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12816
Mulroy, E., Balint, B., Adams, M.E., Campion, T., Merello, M., Bhatia, K.P. (2019). Animals in the Brain. Movement Disorders Clinical Practice, 6 (3), 189-198. doi:10.1002/mdc3.12734
Balint, B., Rispoli, V., Latorre, A., Bhatia, K.P. (2019). Ataxia with Oculomotor Apraxia Type 1—New Mutation, Characteristic Phenotype. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12725
Mulroy, E., Balint, B., Menozzi, E., Latorre, A., Bhatia, K.P. (2019). Benign tremulous parkinsonism of the young-consider Parkin.. Parkinsonism Relat Disord, doi:10.1016/j.parkreldis.2019.05.027
Rocchi, L., Latorre, A., Paparella, G., Menozzi, E., Peppoloni, L., Valero-Cuevas, F., ...Rothwell, J. (2019). Botulinum toxin injections reduce the symptoms of dystonic tremor and improve sensorimotor function for hand dexterity.
Kojović, M., Bhatia, K.P. (2019). Bringing order to higher order motor disorders. Journal of Neurology, doi:10.1007/s00415-018-8974-9
Giagkou, N., Bhatia, K.P., Höglinger, G.U., Stamelou, M. (2019). Chapter Thirteen - Genetic mimics of the non-genetic atypical parkinsonian disorders – the ‘atypical’ atypical. International Review of Neurobiology, 149 327-351. doi:10.1016/bs.irn.2019.10.008
Mulroy, E., Latorre, A., Magrinelli, F., Bhatia, K.P. (2019). Ciliary dysfunction: the hairy explanation of Normal Pressure Hydrocephalus?. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12880
Balint, B., Charlesworth, G., Erro, R., Wood, N.W., Bhatia, K.P. (2019). Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia!. Mov Disord, 34 (4), 589-592. doi:10.1002/mds.27638
Shetty, A.S., Bhatia, K.P., Lang, A.E. (2019). Dystonia and Parkinson's disease: What is the relationship?. Neurobiology of Disease, 132 104462. doi:10.1016/j.nbd.2019.05.001
Relja, M., Miletic, V., Albanese, A., Bhatia, K., Dressler, D.M., Ferreira, J., ...Stamelou, M. (2019). Dystonia in Europe: a survey towards care from patients perspectives.
Menozzi, E., Latorre, A., Balint, B., Bhatia, K.P. (2019). Dystonia in Handcuffs: A Picture Typical of Lesch-Nyhan Syndrome. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12776
Mencacci, N.E., Brockmann, M.M., Pajusalu, S., Atasu, B., Gonzalez-Latapi, P., Schwake, M., ...Simon-Sanchez, J. (2019). Homozygous BZRAP1 mutations cause autosomal recessive dystonia.
Grimm, M.-.J., Respondek, G., Stamelou, M., Arzberger, T., Ferguson, L., Gelpi, E., ...Pantelyat, A. (2019). How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy.. Movement Disorders, doi:10.1002/mds.27666
Mulroy, E., Stamelou, M., Bhatia, K.P. (2019). How to approach a patient with parkinsonism – red flags for atypical parkinsonism. International Review of Neurobiology, 149 1-34. doi:10.1016/bs.irn.2019.10.001
Ganos, C., Zittel, S., Hidding, U., Funke, C., Biskup, S., Bhatia, K.P. (2019). IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizures. Parkinsonism & Related Disorders, 68 57-59. doi:10.1016/j.parkreldis.2019.09.020
Balint, B., Govert, F., Latorre, A., Mulroy, E., Erro, R., Batla, A., ...Bhatia, K. (2019). Longstanding cervical dystonia followed by parkinsonism - coincidence, risk factor or syndromic association?.
Colosimo, C., Bhidayasiri, R., Fheodoroff, K., Bhatia, K., Chung, T.M., Landreau, T., Jacinto, L.J. (2019). Management of Spastic Paresis and Cervical Dystonia: access to Therapeutic Innovations Through an International Program of Practical Courses. Clinical Therapeutics, doi:10.1016/j.clinthera.2019.09.007
Balint, B., Charlesworth, G., Stamelou, M., Carr, L., Mencacci, N.E., Wood, N.W., Bhatia, K.P. (2019). Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy.. Eur J Neurol, doi:10.1111/ene.13956
Corp, D.T., Joutsa, J., Darby, R.R., Delnooz, C.C.S., van de Warrenburg, B.P.C., Cooke, D., ...Batla, A. (2019). Network localization of cervical dystonia based on causal brain lesions. Brain : a journal of neurology, 142 (6), 1660-1674. doi:10.1093/brain/awz112
Tinazzi, M., Squintani, G.M., Bhatia, K.P., Segatti, A., Donato, F., Valeriani, M., Erro, R. (2019). Pain in cervical dystonia: Evidence of abnormal inhibitory control. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2019.06.009
Mulroy, E., Latorre, A., Bhatia, K.P. (2019). Parkinsonism in essential tremor cases: A clinicopathological study-were they really essential tremor?. Movement Disorders, 34 (11), 1749. doi:10.1002/mds.27835
Balint, B., Stephen, C.D., Udani, V., Sankhla, C.S., Barad, N.H., Lang, A.E., Bhatia, K.P. (2019). Paroxysmal Asymmetric Dystonic Arm Posturing—A Less Recognized but Characteristic Manifestation of ATP1A3-related disease. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12747
Berlot, R., Bhatia, K.P., Kojović, M. (2019). Pseudodystonia: A new perspective on an old phenomenon. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2019.02.008
Mainka, T., Erro, R., Rothwell, J., Kühn, A.A., Bhatia, K.P., Ganos, C. (2019). Remission in dystonia - Systematic review of the literature and meta-analysis.. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2019.02.020
Balint, B., Ganos, C., Bhatia, K.P. (2019). Reply to: Tics in Paroxysmal Kinesigenic Dyskinesia. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12783
Bhatia, K., Merello, M. (2019). Response from the Editors RE: DUOPA® is an Excellent Alternative Treatment but with Some Caveats. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12737
Faustino, P.R., Duarte, G.S., Chendo, I., Castro Caldas, A., Reimão, S., Fernandes, R.M., ...Ferreira, J.J. (2019). Risk of Developing Parkinson Disease in Bipolar Disorder: A Systematic Review and Meta-analysis. JAMA Neurology, E1-E7. doi:10.1001/jamaneurol.2019.3446
Bonomo, R., Latorre, A., Bhatia, K.P. (2019). Self-Injurious Behaviour in SCA17: A New Clinical Observation. Tremor and other hyperkinetic movements (New York, N.Y.), 9 doi:10.7916/tohm.v0.672
Brugger, F., Peters, A., Georgiev, D., Kägi, G., Balint, B., Bhatia, K.P., Day, B.L. (2019). Sensory trick efficacy in cervical dystonia is linked to processing of neck proprioception. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2018.11.029
Kolmancic, K., Perellón‐Alfonso, R., Pirtosek, Z., Rothwell, J.C., Bhatia, K., Kojovic, M. (2019). Sex differences in Parkinson's disease: A transcranial magnetic stimulation study. Movement Disorders, doi:10.1002/mds.27870
Jesús, S., Latorre, A., Vinuela, A., Fahn, S., Bhatia, K.P., Balint, B. (2019). Stimulus Sensitive Foot Myoclonus: A Clue to Coeliac Disease. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12753
Cortelli, P., Calandra-Buonaura, G., Benarroch, E.E., Giannini, G., Iranzo, A., Low, P.A., ...Tolosa, E. (2019). Stridor in multiple system atrophy: Consensus statement on diagnosis, prognosis, and treatment. Neurology, 93 (14), 630-639. doi:10.1212/WNL.0000000000008208
Mulroy, E., Balint, B., Latorre, A., Schreglmann, S., Menozzi, E., Bhatia, K.P. (2019). Syringomyelia-Associated Dystonia: Case Series, Literature Review, and Novel Insights. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12772
Gövert, F., Becktepe, J., Balint, B., Rocchi, L., Brugger, F., Garrido, A., ...Elble, R. (2019). Temporal discrimination is altered in patients with isolated asymmetric and jerky upper limb tremor.. Mov Disord, doi:10.1002/mds.27880
Mulroy, E., Bhatia, K.P. (2019). The Gut Microbiome: A Therapeutically Targetable Site of Peripheral Levodopa Metabolism. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12828
Latorre, A., Rocchi, L., Berardelli, A., Bhatia, K.P., Rothwell, J.C. (2019). The interindividual variability of transcranial magnetic stimulation effects: Implications for diagnostic use in movement disorders. Movement Disorders, doi:10.1002/mds.27736
Barbosa, P., Djamshidian, A., O'Sullivan, S.S., de Pablo-Fernandez, E., Korlipara, P., Morris, H.R., ...Lees, A.J. (2019). The long-term outcome of impulsive compulsive behaviours in Parkinson’s disease. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2018-319891
Latorre, A., Rocchi, L., Paparella, G., Manzo, N., Berardelli, A., Rothwell, J., Bhatia, K. (2019). The role of the cerebellum in the pathophysiology of cortical myoclonus: a neurophysiological study..
Mainka, T., Balint, B., Gövert, F., Kurvits, L., van Riesen, C., Kühn, A.A., ...Bhatia, K.P. (2019). The spectrum of involuntary vocalizations in humans: A video atlas. Movement Disorders, doi:10.1002/mds.27855
Latorre, A., Rocchi, L., Berardelli, A., Bhatia, K.P., Rothwell, J.C. (2019). The use of transcranial magnetic stimulation as a treatment for movement disorders: A critical review.. Mov Disord, doi:10.1002/mds.27705
Ganos, C., Martino, D., Espay, A.J., Lang, A.E., Bhatia, K.P., Edwards, M.J. (2019). Tics and functional tic-like movements: Can we tell them apart?. Neurology, doi:10.1212/WNL.0000000000008372
Kresojević, N., Erro, R., Bhatia, K. (2019). Treatment of paroxysmal kinesigenic dyskinesias. In Current Clinical Neurology. (pp. 313-315). .
Latorre, A., Rocchi, L., Stamelou, M., Batla, A., Ciocca, M., Balint, B., ...Bhatia, K.P. (2019). Tremor in motor neuron disease may be central rather than peripheral in origin.. European Journal of Neurology, doi:10.1111/ene.13743
Menozzi, E., Balint, B., Latorre, A., Valente, E.M., Rothwell, J.C., Bhatia, K.P. (2019). Twenty years on: Myoclonus-dystonia and ε-sarcoglycan — neurodevelopment, channel, and signaling dysfunction. Movement Disorders, doi:10.1002/mds.27822
Vollstedt, E.J., Kasten, M., Klein, C., Aasly, J., Adler, C., Ahmad-Annuar, A., ...Alvarez, V. (2019). Using global team science to identify genetic parkinson's disease worldwide. Annals of Neurology, doi:10.1002/ana.25514
Klingelhoefer, L., Chaudhuri, K.R., Kamm, C., Martinez-Martin, P., Bhatia, K., Sauerbier, A., ...Untucht, R. (2019). Validation of a self-completed Dystonia Non-Motor Symptoms Questionnaire. Annals of Clinical and Translational Neurology, doi:10.1002/acn3.50900
Respondek, G., Grimm, M.-.J., Piot, I., Arzberger, T., Compta, Y., Englund, E., ...Giese, A. (2019). Validation of the movement disorder society criteria for the diagnosis of 4-repeat tauopathies. Movement Disorders, doi:10.1002/mds.27872

2018

Kaski, D., Haider, S., Male, A., Radunovich, A., Liu, F., Cordivari, C., ...Bronstein, A.M. (2018). Adult Periodic Alternating Nystagmus Masked by Involuntary Head Movements. Frontiers in Neurology, 9 doi:10.3389/fneur.2018.00326
Cani, I., Latorre, A., Cordivari, C., Balint, B., Bhatia, K.P. (2018). Brachial Neuritis After Botulinum Toxin Injections for Cervical Dystonia: A Need for a Reappraisal?. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12710
Pajusalu, S., Mencacci, N.E., Atasu, B., Rein, R., Puusepp, S., Reinson, K., ...Warner, T.T. (2018). BZRAP1 (RIM-BP1) mutations cause a novel autosomal recessive dystonia syndrome.
Antelmi, E., Rocchi, L., Cocco, A., Erro, R., Latorre, A., Liguori, R., ...Bhatia, K.P. (2018). Cerebellar and brainstem functional abnormalities in patients with primary orthostatic tremor.. Movement disorders : official journal of the Movement Disorder Society, doi:10.1002/mds.27331
Chen, J.C., Macerollo, A., Sadnicka, A., Lu, M.K., Tsai, C.H., Korlipara, P., ...Edwards, M.J. (2018). Cervical dystonia: Normal auditory mismatch negativity and abnormal somatosensory mismatch negativity. Clinical Neurophysiology, 129 (9), 1947-1954. doi:10.1016/j.clinph.2018.05.028
Latorre, A., Salgado, P., Salari, M., Jesuthasan, A., Bhatia, K.P. (2018). Combined Dystonia With Self-Mutilation in 6-Pyruvoyl-Tetrahydropterin Synthase (PTPS) Deficiency: A Case Report. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12698
Nethisinghe, S., Lim, W.N., Ging, H., Zeitlberger, A., Abeti, R., Pemble, S., ...Houlden, H. (2018). Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17. Frontiers in Cellular Neuroscience, 12 doi:10.3389/fncel.2018.00429
Ganos, C., Ferrè, E.R., Marotta, A., Kassavetis, P., Rothwell, J., Bhatia, K.P., Haggard, P. (2018). Cortical inhibitory function in cervical dystonia.. Clinical Neurophysiology, doi:10.1016/j.clinph.2017.11.020
Rocchi, L., Latorre, L., Rothwell, J., Bhatia, K. (2018). Cortical myoclonus explained by cerebellar dysfunction: Evidence from a unique case.
Sadnicka, A., Galea, J.M., Chen, J.-.C., Warner, T.T., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2018). Delineating cerebellar mechanisms in DYT11 myoclonus‐dystonia. Movement Disorders, doi:10.1002/mds.27517
Balint, B., Killaspy, H., Marston, L., Barnes, T., Latorre, A., Joyce, E., ...Erro, R. (2018). Development and clinimetric assessment of a nurse-administered screening tool for movement disorders in psychosis.. BJPsych Open, 4 (5), 404-410. doi:10.1192/bjo.2018.55
Niccolini, F., Wilson, H., Hirschbichler, S., Yousaf, T., Pagano, G., Whittington, A., ...Jaunmuktane, Z. (2018). Disease-related patterns of in vivo pathology in Corticobasal syndrome. European Journal of Nuclear Medicine and Molecular Imaging, doi:10.1007/s00259-018-4104-2
Govert, F., Becktepe, J., Brugger, F., Rocchi, L., Garrido, A., Balint, B., ...Elble, R. (2018). Distinguishing isolated asymmetric limb tremor from essential tremor: An electrophysiological study.
Balint, B., Mencacci, N.E., Valente, E.M., Pisani, A., Rothwell, J., Jankovic, J., ...Bhatia, K.P. (2018). Erratum to: Dystonia (Nature Reviews Disease Primers, (2018), 4, 1, (25), 10.1038/s41572-018-0023-6). Nature Reviews Disease Primers, 4 (1), doi:10.1038/s41572-018-0039-y
Schreglmann, S.R., Bhatia, K.P., Hagele-Link, S., Werner, B., Martin, E., Kagi, G. (2018). Errors in the meta-analysis of outcomes and complications of MRgFUS. NEUROSURGICAL FOCUS, 45 (1), doi:10.3171/2018.3.FOCUS1898
Schreglmann, S.R., Krauss, J., Chang, J.W., Bhatia, K.P., Kägi, G. (2018). Functional lesional neurosurgery for tremor: a systematic review and meta-analysis. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2017-316302
Schreglmann, S.R., Krauss, J.K., Chang, J.W., Bhatia, K.P., Kagi, G. (2018). Functional lesional neurosurgery for tremor: a systematic review and meta-analysis.
Wissel, B.D., Dwivedi, A.K., Merola, A., Chin, D., Jacob, C., Duker, A.P., ...Levy, A. (2018). Functional neurological disorders in Parkinson disease.. Journal of neurology, neurosurgery, and psychiatry, 89 (6), 566-571. doi:10.1136/jnnp-2017-317378
Kolmancic, K., Alfonso, R.P., Pirtosek, Z., Bhatia, K.P., Kojovic, M. (2018). Gender differences in Parkinson's disease: transcranial magnetic stimulation study of newly diagnosed and drug-naive PD patients.
Rossi, M., Balint, B., Millar Vernetti, P., Bhatia, K.P., Merello, M. (2018). Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12635
Erro, R., Rocchi, L., Antelmi, E., Liguori, R., Tinazzi, M., Berardelli, A., ...Bhatia, K.P. (2018). High frequency somatosensory stimulation in dystonia: Evidence for defective inhibitory plasticity. Movement Disorders, doi:10.1002/mds.27470
Sadnicka, A., Stevenson, A., Bhatia, K.P., Rothwell, J.C., Edwards, M.J., Galea, J.M. (2018). High motor variability in DYT1 dystonia is associated with impaired visuomotor adaptation.. Scientific reports, 8 (1), 3653. doi:10.1038/s41598-018-21545-0
Jacinto, L.J., Bhidayasiri, R., Bhatia, K., Colosimo, C., Landreau, T., Chung, T.M. (2018). IMPROVEMENT OF CERVICAL DYSTONIA AND SPASTIC PARESIS MANAGEMENT: ASSESSMENT OF 5 YEARS OF THE INNOVATIVE INTERNATIONAL EDUCATIONAL PROGRAM IXCELLENCE NETWORK (R).
Latorre, A., Rocchi, L., Berardelli, A., Rothwell, J., Bhatia, K. (2018). Is primary writing tremor a form fruste of dystonia?.
Pihlstrøm, L., Schottlaender, L., Chelban, V., Houlden, H., Al-Sarraj, S., Arzberger, T., ...Federoff, M. (2018). LRP10 in α-synucleinopathies. The Lancet Neurology, 17 (12), 1033-1034. doi:10.1016/S1474-4422(18)30407-1
Ganos, C., Rocchi, L., Latorre, A., Hockey, L., Palmer, C., Joyce, E.M., ...Rothwell, J. (2018). Motor cortical excitability during voluntary inhibition of involuntary tic movements.. Mov Disord, doi:10.1002/mds.27479
Balint, B., Vincent, A., Meinck, H.-.M., Irani, S.R., Bhatia, K.P. (2018). Movement disorders with neuronal antibodies: syndromic approach, genetic parallels and pathophysiology. Brain, 141 13-36. doi:10.1093/brain/awx189
Rispoli, V., Schreglmann, S.R., Bhatia, K.P. (2018). Neuroimaging advances in Parkinson's disease. Current Opinion in Neurology, 31 (4), 415-424. doi:10.1097/WCO.0000000000000584
Schreglmann, S., Jaunmuktane, Z., Jung, H., Strand, C., Holton, J., Bhatia, K. (2018). Neuropathology of dopa-responsive dystonia due to Tyrosine hydroxylase deficiency.
Balint, B., Antelmi, E., Mencacci, N.E., Batla, A., Eriksson, S.H., Walker, M.C., ...Bhatia, K.P. (2018). Oculomotor apraxia and disrupted sleep with nocturnal ballistic bouts in ADCY5-related disease. Parkinsonism & Related Disorders, doi:10.1016/j.parkreldis.2018.04.011
Mahlknecht, P., Georgiev, D., Akram, H., Brugger, F., Vinke, S., Zrinzo, L., ...Willeit, P. (2018). Parkinsonian signs in patients with cervical dystonia treated with pallidal deep brain stimulation.. Brain, doi:10.1093/brain/awy217
Wagnon, J.L., Mencacci, N.E., Barker, B.S., Wengert, E.R., Bhatia, K.P., Balint, B., ...Meisler, M.H. (2018). Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonus. Human Mutation, doi:10.1002/humu.23547
Niccolini, F., Mencacci, N.E., Yousaf, T., Rabiner, E.A., Salpietro, V., Pagano, G., ...Gunn, R.N. (2018). PDE10A and ADCY5 mutations linked to molecular and microstructural basal ganglia pathology. Movement Disorders, doi:10.1002/mds.27523
Balint, B., Erro, R., Bhatia, K.P. (2018). Primary or Idiopathic Dystonias (‘Isolated Dystonia’). In Treatment of Dystonia. (pp. 15-19). .
Ricciardi, L., Edwards, M.J., Fasano, A., Bhatia, K.P., Stamelou, M. (2018). Progressive spasticity, supranuclear gaze palsy and postural instability, without parkinsonism: what's in a phenotype?. Journal of the Neurological Sciences, 390 84-86. doi:10.1016/j.jns.2018.04.016
Balint, B., Wiethoff, S., Martino, D., del Gamba, C., Latorre, A., Ganos, C., ...Bhatia, K.P. (2018). Quick Flicks: Association of Paroxysmal Kinesigenic Dyskinesia and Tics. Movement Disorders Clinical Practice, 5 (3), 317-320. doi:10.1002/mdc3.12615
Kassavetis, P., Sadnicka, A., Saifee, T.A., Pareés, I., Kojovic, M., Bhatia, K.P., ...Edwards, M.J. (2018). Reappraising the role of motor surround inhibition in dystonia. Journal of the Neurological Sciences, 390 178-183. doi:10.1016/j.jns.2018.04.015
Batla, A., De Pablo-Fernandez, E., Erro, R., Reich, M., Calandra-Buonaura, G., Barbosa, P., ...Cortelli, P. (2018). Reply to: Young- onset multiple system atrophy. MOVEMENT DISORDERS, 33 (12), 1975-1976. doi:10.1002/mds.27572
Latorre, A., Rocchi, L., Cordivari, C., Berardelli, A., Bhatia, K.P., Rothwell, J.C. (2018). Reply: “Reappraisal of cortical myoclonus: Electrophysiology is the gold standard”. Movement Disorders, 33 (7), 1191. doi:10.1002/mds.27440
Bhidayasiri, R., Bhatia, K., Jacinto, L.J., Chung, T.M., Landreau, T., Colosimo, C. (2018). RESULTS FROM THE INPUT SURVEY: TRAINING IMPACT ON USAGE OF BOTULINUM NEUROTOXIN TYPE A FOR CERVICAL DYSTONIA AND SPASTIC PARESIS MANAGEMENT.
Warner, T.T., Foley, J., Niven, E., Paget, A., Bhatia, K., Farmer, S., ...Bak, T. (2018). Sensitivity and Specificity of the ECAS in Parkinson’s Disease and Progressive Supranuclear Palsy. Parkinson’s Disease, doi:10.1155/2018/2426012
Valente, E.M., Bhatia, K.P. (2018). Solving Mendelian Mysteries: The Non-coding Genome May Hold the Key. Cell, 172 (5), 889-891. doi:10.1016/j.cell.2018.02.022
Salgado, P., Latorre, A., Del Gamba, C., Menozi, E., Balint, B., Bhatia, K.P. (2018). SPG7: The Great Imitator of MSA-C Within the ILOCAs. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12711
Pizza, F., Antelmi, E., Vandi, S., Meletti, S., Erro, R., Baumann, C.R., ...Iranzo, A. (2018). The distinguishing motor features of cataplexy: a study from video-recorded attacks.
Varley, J.A., Webb, A.J.S., Balint, B., Fung, V.S.C., Sethi, K.D., Tijssen, M.A.J., ...Evans, M. (2018). The Movement disorder associated with NMDAR antibody-encephalitis is complex and characteristic: An expert video-rating study. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2018-318584
Erro, R., Balint, B., Bhatia, K.P. (2018). Treatment of Paroxysmal Dystonia. In Treatment of Dystonia. (pp. 292-296). .
Deuschl, G., Bhatia, K.P., Elble, R., Hallett, M. (2018). Understanding the new tremor classification. Movement disorders : official journal of the Movement Disorder Society, doi:10.1002/mds.27368
Erro, R., Bhatia, K.P. (2018). Unravelling of the paroxysmal dyskinesias. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2018-318932
Batla, A., De Pablo-Fernandez, E., Erro, R., Reich, M., Calandra-Buonaura, G., Barbosa, P., ...Cortelli, P. (2018). Young-onset multiple system atrophy: Clinical and pathological features.. Mov Disord, 33 (7), 1099-1107. doi:10.1002/mds.27450

2017

Hirschbichler, S.T., Erro, R., Ganos, C., Stamelou, M., Batla, A., Balint, B., Bhatia, K.P. (2017). "Atypical" atypical parkinsonism: Critical appraisal of a cohort.. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2016.12.006
di Biase, L., Brittain, J.S., Shah, S.A., Pedrosa, D.J., Cagnan, H., Mathy, A., ...Bhatia, K. (2017). A New Neurophysiological Tool for Differential Diagnosis in Tremor Syndromes: The Tremor Stability Index.
Carecchio, M., Mencacci, N.E., Iodice, A., Pons, R., Panteghini, C., Zorzi, G., ...Jankovic, J. (2017). ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients. PARKINSONISM & RELATED DISORDERS, 41 37-43. doi:10.1016/j.parkreldis.2017.05.004
Bhatia, K., Erro, R., Stamelou, M. (2017). Case Studies in Movement Disorders. Cambridge University Press.
Pauls, K.A.M., Krauss, J.K., Kämpfer, C.E., Kühn, A.A., Schrader, C., Südmeyer, M., ...Boller, J.K. (2017). Causes of failure of pallidal deep brain stimulation in cases with pre-operative diagnosis of isolated dystonia. Parkinsonism and Related Disorders, doi:10.1016/j.parkreldis.2017.06.023
Schreglmann, S.R., Bhatia, K.P., Stamelou, M. (2017). Chapter Five - Advances in the Clinical Differential Diagnosis of Parkinson's Disease. International Review of Neurobiology, doi:10.1016/bs.irn.2017.01.007
Bhatia, K.P., Stamelou, M. (2017). Chapter Forty-Six - Nonmotor Features in Atypical Parkinsonism. International Review of Neurobiology, doi:10.1016/bs.irn.2017.06.001
Höglinger, G.U., Respondek, G., Stamelou, M., Kurz, C., Josephs, K.A., Lang, A.E., ...Whitwell, J.L. (2017). Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria. Movement Disorders, 32 (6), 853-864. doi:10.1002/mds.26987
Contarino, M.F., Van den Dool, J., Balash, Y., Bhatia, K., Giladi, N., Koelman, J.H., ...Relja, M. (2017). Clinical Practice: evidence-Based Recommendations for the Treatment of Cervical Dystonia with Botulinum Toxin. FRONTIERS IN NEUROLOGY, 8 doi:10.3389/fneur.2017.00035
Bhatia, K.P., Bain, P., Bajaj, N., Elble, R.J., Hallett, M., Louis, E.D., ...Deuschl, G. (2017). Consensus Statement on the classification of tremors, from the task force on tremor of the International Parkinson and Movement Disorder Society. Movement Disorders, doi:10.1002/mds.27121
Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M.E., Grozeva, D., Joseph, A.P., ...Barral, S. (2017). Corrigendum: Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.. Nature genetics, 49 (6), 969. doi:10.1038/ng0617-969b
Jansen, I.E., Ye, H., Heetveld, S., Lechler, M.C., Michels, H., Seinstra, R.I., ...Majounie, E. (2017). Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.. Genome Biology, 18 (1), 22. doi:10.1186/s13059-017-1147-9
Kägi, G., Ruge, D., Brugger, F., Katschnig, P., Sauter, R., Fiorio, M., ...Bhatia, K.P. (2017). Endophenotyping in idiopathic adult onset cervical dystonia.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 128 (7), 1142-1147. doi:10.1016/j.clinph.2017.04.007
Espay, A.J., Lang, A.E., Erro, R., Merola, A., Fasano, A., Berardelli, A., Bhatia, K.P. (2017). Essential Pitfalls in "Essential" Tremor. MOVEMENT DISORDERS, 32 (3), 325-331. doi:10.1002/mds.26919
Robak, L.A., Jansen, I.E., van Rooij, J., Uitterlinden, A.G., Kraaij, R., Jankovic, J., ...IPDGC Consortium, m.e.m.b.e.r.s. (2017). Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease.. Brain : a journal of neurology, doi:10.1093/brain/awx285
Abbas, M.M., Govindappa, S.T., Sheerin, U.-.M., Bhatia, K.P., Muthane, U.B. (2017). Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation. MOVEMENT DISORDERS, 32 (1), 132-135. doi:10.1002/mdc3.12353
Schreglmann, S., Krauss, J.K., Chang, J.W., Bhatia, K.P., Kagi, G. (2017). Functional lesional neurosurgery for tremor - a protocol for a systematic review and meta-analysis. BMJ OPEN, 7 (5), doi:10.1136/bmjopen-2016-015409
Schreglmann, S.R., Krauss, J.K., Chang, J.W., Martin, E., Werner, B., Bauer, R., ...Kägi, G. (2017). Functional lesional neurosurgery for tremor: back to the future?. Journal of Neurology, Neurosurgery, and Psychiatry, doi:10.1136/jnnp-2017-316301
Wissel, B.D., Dwivedi, A.K., Chin, D., Merola, A., Jacob, C., Duker, A.P., ...Levy, A. (2017). Functional neurological features in Parkinson disease: a multicenter case-control study.
Witoelar, A., Jansen, I.E., Wang, Y., Desikan, R.S., Gibbs, J.R., Blauwendraat, C., ...Schork, A.J. (2017). Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.. JAMA neurology, doi:10.1001/jamaneurol.2017.0469
Rocchi, L., Erro, R., Antelmi, E., Berardelli, A., Tinazzi, M., Liguori, R., ...Rothwell, J. (2017). High frequency somatosensory stimulation increases sensori-motor inhibition and leads to perceptual improvement in healthy subjects.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 128 (6), 1015-1025. doi:10.1016/j.clinph.2017.03.046
Antelmi, E., Di Stasio, F., Rocchi, L., Erro, R., Liguori, R., Ganos, C., ...Rothwell, J. (2017). Impaired eye blink classical conditioning distinguishes dystonic patients with and without tremor (vol 31, pg 23, 2016). PARKINSONISM & RELATED DISORDERS, 35 102. doi:10.1016/j.parkreldis.2016.10.016
Wilson, H., Niccolini, F., Hirschbichler, S., Pagano, G., Erro, R., Yousaf, T., ...Bhatia, K. (2017). In vivo tau and amyloid pathology in Corticobasal Degeneration (CBD).
Bhatia, K.P., Chaudhuri, K.R., Stamelou, M. (Eds.), (2017). INTERNATIONAL REVIEW OF NEUROBIOLOGY Parkinson's Disease VOLUME 132 PREFACE. ELSEVIER ACADEMIC PRESS INC.
Niccolini, F., Wilson, H., Hirschbichler, S., Pagano, G., Erro, R., Yousaf, T., ...Rabiner, E. (2017). In-vivo evaluation of tau and amyloid pathology in Corticobasal Syndrome.
Arber, C., Angelova, P.R., Wiethoff, S., Tsuchiya, Y., Mazzacuva, F., Preza, E., ...Abramov, A.Y. (2017). iPSC-derived neuronal models of PANK2-associated neurodegeneration reveal mitochondrial dysfunction contributing to early disease.. PLoS ONE, 12 (9), e0184104. doi:10.1371/journal.pone.0184104
Fheodoroff, K., Bhidayasiri, R., Jacinto, L.J., Chung, T.M., Bhatia, K., Landreau, T., Colosimo, C. (2017). Ixcellence network®: An international educational network to improve current practice in the management of cervical dystonia or spastic paresis by botulinum toxin injection. Functional Neurology, 32 (2), 103-110. doi:10.11138/FNeur/2017.32.2.103
Niccolini, F., Mencacci, N., Rabiner, E., Salpietro, V., Pagano, G., Balint, B., ...Bhatia, K. (2017). Loss of PDE10A expression in patients with PDE10A and ADYC5 mutations.
Niccolini, F., Mencacci, N.E., Rabiner, E., Salpietro, V., Pagano, G., Balint, B., ...Bhatia, K.P. (2017). Loss of PDE10A expression in patients with PDE10A and ADYC5 mutations.
Sadnicka, A., Daum, C., Cordivari, C., Bhatia, K.P., Rothwell, J.C., Manohar, S., Edwards, M.J. (2017). Mind the gap: temporal discrimination and dystonia. European Journal of Neurology, 24 (6), 796-806. doi:10.1111/ene.13293
Schreglmann, S.R., Riederer, F., Galovic, M., Ganos, C., Kägi, G., Waldvogel, D., ...Krasemann, E. (2017). Movement disorders in genetically confirmed mitochondrial disease and the putative role of the cerebellum.. Movement disorders : official journal of the Movement Disorder Society, doi:10.1002/mds.27174
Hywel, B., Ellis, R.J.B., Bhatia, K.P., Doran, M. (2017). MYOCLONUS DYSTONIA AND RUSSELL-SILVER SYNDROME IN A PATIENT WITH A MICRODELETION OF CHROMOSOME 7Q.
Brugger, F., Kägi, G., Pandolfo, M., Mencacci, N.E., Batla, A., Wiethoff, S., Bhatia, K.P. (2017). Neurodegeneration With Brain Iron Accumulation (NBIA) Syndromes Presenting With Late-Onset Craniocervical Dystonia: An Illustrative Case Series‎. Movement Disorders Clinical Practice, 4 (2), 254-257. doi:10.1002/mdc3.12393
Antelmi, E., Erro, R., Rocchi, L., Liguori, R., Tinazzi, M., Di Stasio, F., ...Bhatia, K.P. (2017). Neurophysiological correlates of abnormal somatosensory temporal discrimination in dystonia. Movement Disorders, 32 (1), 141-148. doi:10.1002/mds.26804
Geissler, J.M., Nalls, M., Plagnol, V., Hernandez, D.G., Sharma, M., Sheerin, U.M., ...Lesage, S. (2017). No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs. ADHD Attention Deficit and Hyperactivity Disorders, 1-7. doi:10.1007/s12402-017-0219-8
Erro, R., Tinazzi, M., Morgante, F., Bhatia, K.P. (2017). Non-invasive brain stimulation for dystonia: therapeutic implications. European Journal of Neurology, 24 (10), e64-1228. doi:10.1111/ene.13363
Bhatia, K.P., Stamelou, M. (2017). Nonmotor Features in Atypical Parkinsonism. In Chaudhuri, K.R., Titova, N. (Eds.), NONMOTOR PARKINSON'S: THE HIDDEN FACE - MANAGEMENT AND THE HIDDEN FACE OF RELATED DISORDERS. (pp. 1285-1301). ELSEVIER ACADEMIC PRESS INC.
Balint, B., Charlesworth, G., Stamelou, M., Carr, L., Wood, N., Bhatia, K. (2017). NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy.
Balint, B., Charlesworth, G., Stamelou, M., Carr, L., Wood, N.W., Bhatia, K. (2017). NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy.
Kaji, R., Bhatia, K., Graybiel, A.M. (2017). Pathogenesis of dystonia: is it of cerebellar or basal ganglia origin?. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2017-316250
Kojovic, M., Kassavetis, P., Pareés, I., Georgiev, D., Rocchi, L., Balint, B., ...Bhatia, K. (2017). Pathophysiological heterogeneity in Parkinson's disease: Neurophysiological insights from LRRK2 mutations.. Movement Disorders, doi:10.1002/mds.27091
Bhatia, K.P., Chaudhuri, K.R., Stamelou, M. (2017). Preface. International Review of Neurobiology, 132 xv. doi:10.1016/S0074-7742(17)30078-8
Latorre, A., Rocchi, L., Berardelli, A., Bhatia, K., Cordivari, C. (2017). Reappraisal of cortical myoclonus: A retrospective study of clinical neurophysiology.
Latorre, A., Rocchi, L., Berardelli, A., Rothwell, J.C., Bhatia, K.P., Cordivari, C. (2017). Reappraisal of cortical myoclonus: A retrospective study of clinical neurophysiology.. Movement disorders : official journal of the Movement Disorder Society, doi:10.1002/mds.27234
Pizza, F., Antelmi, E., Vandi, S., Meletti, S., Erro, R., Baumann, C.R., ...Iranzo, A. (2017). THE DISTINGUISHING MOTOR FEATURES OF CATAPLEXY: A STUDY FROM VIDEO RECORDED ATTACKS.
Erro, R., Bhatia, K.P., Espay, A.J., Striano, P. (2017). The epileptic and nonepileptic spectrum of paroxysmal dyskinesias: Channelopathies, synaptopathies, and transportopathies.. Movement Disorders, doi:10.1002/mds.26901
Skorvanek, M., Bhatia, K.P. (2017). The Skin and Parkinson's Disease: Review of Clinical, Diagnostic, and Therapeutic Issues. MOVEMENT DISORDERS, 32 (1), 21-31. doi:10.1002/mdc3.12425
Jinnah, H.A., Albanese, A., Bhatia, K.P., Cardoso, F., Da Prat, G., de Koning, T.J., ...Gershanik, O. (2017). Treatable inherited rare movement disorders. Movement Disorders, doi:10.1002/mds.27140
Gatto, E., Jinnah, H., Espay, A., Jankovic, J., Bhatia, K., Rodriguez, M., ...Albanese, A. (2017). Treatable rare movement disorders.
Latorre, A., Stamelou, M., Rocchi, L., Ciocca, M., Sidle, K., Rothwell, J., Bhatia, K. (2017). Tremor in Motorneuron Disease: Central or Peripheral Origin.
di Biase, L., Brittain, J.-.S., Shah, S.A., Pedrosa, D.J., Cagnan, H., Mathy, A., ...Mir, P. (2017). Tremor stability index: a new tool for differential diagnosis in tremor syndromes (vol 140, pg 1977, 2017). BRAIN, 140 doi:10.1093/brain/awx160
di Biase, L., Brittain, J.-.S., Shah, S.A., Pedrosa, D.J., Cagnan, H., Mathy, A., ...Timmerman, L. (2017). Tremor stability index: a new tool for differential diagnosis in tremor syndromes.. Brain : a journal of neurology, doi:10.1093/brain/awx104
Schreglmann, S.R., Bauer, R., Hagele-Link, S., Bhatia, K.P., Natchev, P., Wegener, N., ...Kagi, G. (2017). Unilateral cerebellothalamic tract ablation in essential tremor by MRI-guided focused ultrasound. NEUROLOGY, 88 (14), 1329-1333. doi:10.1212/WNL.0000000000003795
Respondek, G., Kurz, C., Arzberger, T., Compta, Y., Englund, E., Ferguson, L.W., ...Meissner, W.G. (2017). Which ante mortem clinical features predict progressive supranuclear palsy pathology?. Movement Disorders, doi:10.1002/mds.27034

2016

Hirschbichler, S.T., Erro, R., Stamelou, M., Ganos, C., Balint, B., Bhatia, K.P. (2016). "Atypical" atypical Parkinsonism.
Albanese, A., Bhatia, K., DeLong, M.R., Fahn, S., Fung, V.S.C., Hallett, M., ...Teller, J.K. (2016). “Complex” dystonia is not a category in the new 2013 consensus classification. Movement Disorders, 31 (11), 1758-1759. doi:10.1002/mds.26764
Sailer, A., Scholz, S.W., Nalls, M.A., Schulte, C., Federoff, M., Price, T.R., ...Mok, K. (2016). A genome-wide association study in multiple system atrophy.. Neurology, doi:10.1212/WNL.0000000000003221
Balint, B., Killaspy, H., Barnes, T.R.E., Freemantle, N., Joyce, E., Martino, D., Bhatia, K.P. (2016). A survey of movement disorders in a large sample of patients treated with antipsychotic medication.
Fong, P.-.Y., Edwards, M.J., Lu, C.-.S., Chen, R.-.S., Rothwell, J.C., Bhatia, K.P., Huang, Y.-.Z. (2016). Abnormal blink reflex recovery cycle in manifesting and nonmanifesting carriers of the DYT1 gene mutation. NEUROREPORT, 27 (14), 1046-1049. doi:10.1097/WNR.0000000000000653
Macerollo, A., Chen, J.C., Parees, I., Sadnicka, A., Kassavetis, P., Bhatia, K.P., ...Edwards, M.J. (2016). Abnormal movement-related suppression of sensory evoked potentials in upper limb dystonia. EUROPEAN JOURNAL OF NEUROLOGY, 23 (3), 562-568. doi:10.1111/ene.12890
Morgan, J.C., Kurek, J.A., Davis, J., Sethi, K.D., Mencacci, N.E., Erro, R., Bhatia, K.P. (2016). ADCY5 mutations are another cause of benign hereditary chorea. Neurology, 86 (10), 978-979. doi:10.1212/WNL.0000000000002479
Klettner, A., Richert, E., Kuhlenbaeumer, G., Noelle, B., Bhatia, K.P., Deuschl, G., ...Schneider, S.A. (2016). Alpha synuclein and crystallin expression in human lens in Parkinson's disease. MOVEMENT DISORDERS, 31 (4), 600-601. doi:10.1002/mds.26557
Bhatia, K., Colosimo, C., Bhidayasiri, R., Chung, T.M., Jacinto, L.J., Landreau, T., Fheodoroff, K. (2016). An International Medical Education Network for Physicians Treating Cervical Dystonia and Spasticity.
Stamelou, M., Bhatia, K.P. (2016). Atypical parkinsonism - new advances. CURRENT OPINION IN NEUROLOGY, 29 (4), 480-485. doi:10.1097/WCO.0000000000000355
Balint, B., Meinck, H.M., Bhatia, K.P. (2016). Axial Dystonia Mimicking Stiff Person Syndrome. Movement Disorders Clinical Practice, 3 (2), 176-179. doi:10.1002/mdc3.12249
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Bhatia, K., Erro, R., Gardiner, A., Jaffer, F.Z., Stamelou, M., Walker, M., ...Houlden, H. (2016). Clinical and Genetic Heterogeneity of Paroxysmal Dyskinesias.
Erro, R., Gardiner, A., Jaffer, F., Stamelou, M., Kullmann, D.M., Walker, M.C., ...Bhatia, K. (2016). Clinical and genetic heterogeneity of paroxysmal dyskinesias.
Balint, B., Erro, R., Bhatia, K. (2016). Conjugal Parkinson's disease - real or chance?.
Balint, B., Erro, R., Brugger, F., Jha, A., Batla, A., Ganos, C., ...Bhatia, K.P. (2016). Conjugal Parkinson's disease - Real or chance?. Parkinsonism Relat Disord, doi:10.1016/j.parkreldis.2016.10.003
Shakkottai, V.G., Batla, A., Bhatia, K., Dauer, W.T., Dresel, C., Niethammer, M., ...Jinnah, H.A. (2016). Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.. Cerebellum, 16 (2), 577-594. doi:10.1007/s12311-016-0825-6
Mencacci, N.E., Kamsteeg, E.-.J., Nakashima, K., R'Bibo, L., Lynch, D.S., Balint, B., ...Suzuki, K. (2016). De Novo Mutations in PDE1 0A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions. AMERICAN JOURNAL OF HUMAN GENETICS, 98 (4), 763-771. doi:10.1016/j.ajhg.2016.02.015
Mencacci, N.E., Kamsteeg, E.J., R'Bibo, L., Lynch, D., Balint, B., Willemsen, M., ...Meyer, E. (2016). De novo mutations in PDE10A cause childhood-onset chorea with bilateral striatal lesions.
Batla, A., Tai, X.Y., Schottlaender, L., Erro, R., Balint, B., Bhatia, K.P. (2016). Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes.. Parkinsonism Relat Disord, doi:10.1016/j.parkreldis.2016.12.024
Rizig, M., Jonvik, H., Foltynie, T., Limousin, P., Bhatia, K., Warner, T., ...Wood, N. (2016). DEEP PHENOTYPING OF THE G2019S LRRK2 MUTATION IN PARKINSON'S DISEASE: UCL COHORT.
Kassavetis, P., Saifee, T.A., Roussos, G., Drougkas, L., Kojovic, M., Rothwell, J.C., ...Bhatia, K.P. (2016). Developing a Tool for Remote Digital Assessment of Parkinson's Disease. Movement Disorders Clinical Practice, 3 (1), 59-64. doi:10.1002/mdc3.12239
Brugger, F., Peters, A., Georgiev, D., Kagi, G., Balint, B., Bhatia, K.P., Day, B. (2016). Differences in processing proprioceptive input from the neck muscles may explain the benefit from sensory tricks in patients with idiopathic cervical dystonia.
Sadnicka, A., Edwards, M.J., Bhatia, K.P. (2016). Dystonia. In Challenging Concepts in Neurology Cases with Expert Commentary. Oxford University Press.
Schneider, S.A., Erro, R., Bhatia, K.P. (2016). DYT10, paroxysmal kinesiogenic dyskinesia-PKD. In The Curated Reference Collection in Neuroscience and Biobehavioral Psychology. (pp. 429-431). .
Schneider, S.A., Erro, R., Bhatia, K.P. (2016). DYT8, paroxysmal non-kinesigenic dyskinesia-PNKD. In The Curated Reference Collection in Neuroscience and Biobehavioral Psychology. (pp. 424-426). .
Schneider, S.A., Bhatia, K.P. (2016). DYT9, paroxysmal dyskinesia with spasticity. In The Curated Reference Collection in Neuroscience and Biobehavioral Psychology. (pp. 427-428). .
Erro, R., Balint, B., Kurian, M.A., Brugger, F., Picillo, M., Barone, P., ...Pellecchia, M.T. (2016). Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes. Movement Disorders Clinical Practice, 4 (1), 125-128. doi:10.1002/mdc3.12319
Kueppers, S., Daskalopoulos, I., Jha, A., Fragopanagos, N.F., Kassavetis, P., Nomikou, E., ...Luchini, M.U. (2016). From wellness to medical diagnostic apps: The Parkinson’s disease case.
Kara, E., Tucci, A., Manzoni, C., Lynch, D.S., Elpidorou, M., Bettencourt, C., ...Haridy, N.A. (2016). Genetic and phenotypic characterization of complex hereditary spastic paraplegia. BRAIN, 139 1904-1918. doi:10.1093/brain/aww111
Erro, R., Rocchi, L., Antelmi, E., Palladino, R., Tinazzi, M., Rothwell, J., Bhatia, K.P. (2016). High frequency repetitive sensory stimulation improves temporal discrimination in healthy subjects. CLINICAL NEUROPHYSIOLOGY, 127 (1), 817-820. doi:10.1016/j.clinph.2015.06.023
Balint, B., Bhatia, K.P. (2016). Hot topic: PNKP mutations cause ataxia with oculomotor apraxia type 4.. Movement disorders : official journal of the Movement Disorder Society, 31 (4), 500.
Brugger, F., Balint, B., Antelmi, E., Bhatia, K.P. (2016). Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC) is a Differential Diagnosis for Pallidopyramidal Syndromes with Thin Corpus Callosum. Movement Disorders Clinical Practice, doi:10.1002/mdc3.12367
Heywood, W.E., Galimberti, D., Bliss, E., Sirka, E., Paterson, R.W., Magdalinou, N.K., ...Fenoglio, C. (2016). Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay (vol 10, 64, 2015). MOLECULAR NEURODEGENERATION, 11 doi:10.1186/s13024-016-0086-3
Antelmi, E., Di Stasio, F., Rocchi, L., Erro, R., Liguori, R., Ganos, C., ...Rothwell, J. (2016). Impaired eye blink classical conditioning distinguishes dystonic patients with and without tremor.. Parkinsonism & related disorders, doi:10.1016/j.parkreldis.2016.06.011
Ricciardi, L., Ferrazzano, G., Demartini, B., Morgante, F., Erro, R., Ganos, C., ...Edwards, M. (2016). Know thyself: Exploring interoceptive sensitivity in Parkinson's disease. JOURNAL OF THE NEUROLOGICAL SCIENCES, 364 110-115. doi:10.1016/j.jns.2016.03.019
Hopfner, F., Haubenberger, D., Galpern, W.R., Gwinn, K., Van't Veer, A., White, S., ...Ondo, W. (2016). Knowledge gaps and research recommendations for essential tremor. PARKINSONISM & RELATED DISORDERS, 33 27-35. doi:10.1016/j.parkreldis.2016.10.002
Lesage, S., Drouet, V., Majounie, E., Deramecourt, V., Jacoupy, M., Nicolas, A., ...Ciura, S. (2016). Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. AMERICAN JOURNAL OF HUMAN GENETICS, 98 (3), 500-513. doi:10.1016/j.ajhg.2016.01.014
Batla, A., Parees, I., Edwards, M.J., Stamelou, M., Bhatia, K.P., Panicker, J.N. (2016). Lower urinary tract dysfunction in patients with functional movement disorders. JOURNAL OF THE NEUROLOGICAL SCIENCES, 361 192-194. doi:10.1016/j.jns.2015.12.048
Valadas, A., Contarino, M.-.F., Albanese, A., Bhatia, K.P., Falup-Pecurariu, C., Forsgren, L., ...Kostic, V.S. (2016). Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromes. EUROPEAN JOURNAL OF NEUROLOGY, 23 (4), 772-779. doi:10.1111/ene.12940
Erro, R., Hirschbichler, S.T., Ricciardi, L., Ryterska, A., Antelmi, E., Ganos, C., ...Bhatia, K.P. (2016). Mental rotation and working memory in musicians’ dystonia. Brain and Cognition, 109 124-129. doi:10.1016/j.bandc.2016.09.008
Sadnicka, A., Daum, C., Cordivari, C., Bhatia, K.P., Rothwell, J.C., Manohar, S., Edwards, M.J. (2016). Mind the gap: Temporal discrimination and cervical dystonia.
Sadnicka, A., Stevenson, A., Rothwell, J.C., Bhatia, K.P., Galea, J., Edwards, M.J. (2016). Motor variability and learning indices in DYT1 dystonia.
Bhatia, K., Cordivari, C., Edwards, M., Foltynie, T., Hariz, M., Korlipara, P., ...Warner, T. (2016). Movement Disorders. In Neurology: A Queen Square Textbook: Second Edition. (pp. 187-220). .
Meyer, E., Carss, K.J., Rankin, J., Nichols, J.M., Grozeva, D., Joseph, A.P., ...Barral, S. (2016). Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia.. Nat Genet, doi:10.1038/ng.3740
Bhatia, K., Merello, M. (2016). New Developments for MDCP. Movement Disorders Clinical Practice, 3 (1), 3-. doi:10.1002/mdc3.12332
Smith, M., Seth, J., Batla, A., Hofereiter, J., Bhatia, K.P., Panicker, J.N. (2016). Nocturia in Patients With Parkinson's Disease. Movement Disorders Clinical Practice, 3 (2), 168-172. doi:10.1002/mdc3.12279
Erro, R., Bhatia, K.P. (2016). Novel movement disorder society-Parkinson's disease criteria: What about SWEDD and genetic forms?. MOVEMENT DISORDERS, 31 (3), 431. doi:10.1002/mds.26538
Barow, E., Schneider, S.A., Bhatia, K.P., Ganos, C. (2016). Oculogyric crises: Etiology, pathophysiology and therapeutic approaches.. Parkinsonism Relat Disord, 36 3-9. doi:10.1016/j.parkreldis.2016.11.012
Georgiev, D., Mahlknecht, P., Brugger, F., Vinke, S., Zacharia, A., Grover, T., ...Jahanshahi, M. (2016). Parkinsonian symptoms in patients with cervical dystonia treated with bilateral pallidal deep brain stimulation: A controlled study.
Balint, B., Erro, R., Salpietro, V., Houlden, H., Bhatia, K.P. (2016). PKD or Not PKD: That is the question. Annals of neurology, 80 (1), 167-168. doi:10.1002/ana.24668
Ganos, C., Edwards, M.J., Bhatia, K.P. (2016). Posttraumatic functional movement disorders.. Handb Clin Neurol, 139 499-507. doi:10.1016/B978-0-12-801772-2.00041-2
Stamelou, M., Schoepe, J., Wagenpfeil, S., Del Ser, T., Bang, J., Lobach, I.Y., ...Boxer, A. (2016). Power calculations and placebo effect for future clinical trials in progressive supranuclear palsy. MOVEMENT DISORDERS, 31 (5), 742-747. doi:10.1002/mds.26580
Kinghorn, K.J., Castillo-Quan, J.I., Li, L., Bhatia, K.P., Abramov, A.Y., Hardy, J., Partridge, L. (2016). Reply: Glial mitochondropathy in infantile neuroaxonal dystrophy: pathophysiological and therapeutic implications. BRAIN, 139 doi:10.1093/brain/aww185
Hoeglinger, G., Respondek, G., Stamelou, M., Kurz, C., Josephs, K., Lang, A., ...Whitwell, J. (2016). Revised clinical diagnostic criteria for progressive supranuclear palsy (PSP).
Antelmi, E., Erro, R., Rocchi, L., Liguori, R., Tinazzi, M., Rothwell, J., Bhatia, K. (2016). Sensory gating and inhibition in dystonia.
Charlesworth, G., Balint, B., Mencacci, N.E., Carr, L., Wood, N.W., Bhatia, K.P. (2016). SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy.. Movement Disorders, doi:10.1002/mds.26716
Balint, B., Bhatia, K.P. (2016). SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia. Movement Disorders, doi:10.1002/mds.26821
Balint, B., Bhatia, K.P. (2016). Stiff person syndrome and other immune-mediated movement disorders - new insights. CURRENT OPINION IN NEUROLOGY, 29 (4), 496-506. doi:10.1097/WCO.0000000000000351
Balint, B., Bhatia, K.P. (2016). T1-weighted basal ganglia hyperintensities due to gadolinium deposition - a cautionary note. PARKINSONISM & RELATED DISORDERS, 32 135-136. doi:10.1016/j.parkreldis.2016.09.017
Ganos, C., Crowe, B., Stamelou, M., Kresojevic, N., Lukic, M.J., Bras, J., ...Batla, A. (2016). The clinical syndrome of dystonia with anarthria/aphonia. PARKINSONISM & RELATED DISORDERS, 24 20-27. doi:10.1016/j.parkreldis.2016.01.022
Ganos, C., Maugest, L., Apartis, E., Gasca-Salas, C., Caceres-Redondo, M.T., Erro, R., ...Degos, B. (2016). The long-term outcome of orthostatic tremor. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 87 (2), 167-172. doi:10.1136/jnnp-2014-309942
Erro, R., Bhatia, K.P., Esposito, M., Cordivari, C. (2016). The role of polymyography in the treatment of cervical dystonia. JOURNAL OF NEUROLOGY, 263 (8), 1663-1664. doi:10.1007/s00415-016-8202-4
Bloem, B.R., Voermans, N.C., Aerts, M.B., Bhatia, K.P., van Engelen, B.G., van de Warrenburg, B.P. (2016). The wrong end of the telescope: neuromuscular mimics of movement disorders (and vice versa).. Practical neurology, 16 (4), 264-269. doi:10.1136/practneurol-2015-001311
Haubenberger, D., Abbruzzese, G., Bain, P.G., Bajaj, N., Benito-León, J., Bhatia, K.P., ...Louis, E.D. (2016). Transducer-based evaluation of tremor. Movement Disorders, 31 (9), 1327-1336. doi:10.1002/mds.26671
Schreglmann, S.R., Hagele-Link, S., Bauer, R., Bhatia, K.P., Natchev, P., Wegener, N., ...Kagi, G. (2016). Unilateral ablation of the cerebellothalamic tract in essential tremor by MRI-guided high intensity focused ultrasound.
Schwingenschuh, P., Saifee, T., Katschnig-Winter, P., Macerollo, A., Koegl-Wallner, M., Culea, V., ...Seiler, S. (2016). Validation of "laboratory-supported" criteria for functional (psychogenic) tremor.. Movement Disorders, doi:10.1002/mds.26525
Brugger, F., Bhatia, K.P., Besag, F.M.C. (2016). Valproate-Associated Parkinsonism: A Critical Review of the Literature. CNS DRUGS, 30 (6), 527-540. doi:10.1007/s40263-016-0341-8
Erro, R., Schneider, S.A., Stamelou, M., Quinn, N.P., Bhatia, K.P. (2016). What do patients with scans without evidence of dopaminergic deficit (SWEDD) have? New evidence and continuing controversies. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 87 (3), 319-323. doi:10.1136/jnnp-2014-310256

2015

Erro, R., Antelmi, E., Bhatia, K.P. (2015). "A disorder which occurs on standing": The Earliest Account of Orthostatic Tremor by Pazzaglia. Movement Disorders Clinical Practice, 2 (1), 39-40. doi:10.1002/mdc3.12127
Mencacci, N.E., Rubio-Agusti, I., Zdebik, A., Asmus, F., Ludtmann, M.H., Ryten, M., ...Bettencourt, C. (2015). A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia. Am J Hum Genet, 96 (6), 938-947. doi:10.1016/j.ajhg.2015.04.008
Mencacci, N.E., Rubio-Augusti, I., Zdebik, A., Asmus, F., Ludtmann, M., Hauser, A.K., ...Soutar, M. (2015). A missense mutation in the KCTD17 gene causes autosomal dominant myoclonus-dystonia.
Erro, R., Hersheson, J., Houlden, H., Bhatia, K.P. (2015). A novel TUBB4A mutation suggests that genotype-phenotype correlation of H-ABC syndrome needs to be revisited. BRAIN, 138 E370-U5. doi:10.1093/brain/awu403
Magdalinou, N.K., Paterson, R., Schott, J., Fox, N., Mummery, C., Blennow, K., ...Warner, T. (2015). A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromes. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp-2014-309562
Demartini, B., Ricciardi, L., Parees, I., Ganos, C., Bhatia, K.P., Edwards, M.J. (2015). A positive diagnosis of functional (psychogenic) tics.. EUROPEAN JOURNAL OF NEUROLOGY, 22 (3), 527-U52. doi:10.1111/ene.12609
Kun-Rodrigues, C., Ganos, C., Guerreiro, R., Schneider, S.A., Schulte, C., Lesage, S., ...International Parkinson's Disease Genomics Consortium, (.I.P.D.G.C.). (2015). A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. Human Molecula Genetics, 24 (23), 6711-6720. doi:10.1093/hmg/ddv376
Macerollo, A., Saifee, T.A., Kassavetis, P., Pilurzi, G., Schneider, S.A., Edwards, M.J., Bhatia, K.P. (2015). Abnormalities of Masseteric Inhibitory Reflex in Hereditary Geniospasm: Evidence for a Brainstem Myoclonus. Movement Disorders Clinical Practice, 2 (1), 49-52. doi:10.1002/mdc3.12097
Mencacci, N.E., Erro, R., Wiethoff, S., Hersheson, J., Ryten, M., Balint, B., ...Houlden, H. (2015). ADCY5 mutations are another cause of benign hereditary chorea. Neurology, 85 (1), 80-88. doi:10.1212/WNL.0000000000001720
Erro, R., Mencacci, N.E., Hersheson, J., Wiethoff, S., Balint, B., Ganos, C., ...Wood, N.W. (2015). ADCY5 mutations can cause benign hereditary chorea.
Sadnicka, A., Teo, J.T., Kojovic, M., Pareés, I., Saifee, T.A., Kassavetis, P., ...Mencacci, N.E. (2015). All in the blink of an eye: new insight into cerebellar and brainstem function in DYT1 and DYT6 dystonia.. EUROPEAN JOURNAL OF NEUROLOGY, 22 (5), 762-767. doi:10.1111/ene.12521
Comella, C., Bhatia, K. (2015). An international survey of patients with cervical dystonia. JOURNAL OF NEUROLOGY, 262 (4), 837-848. doi:10.1007/s00415-014-7586-2
Schottlaender, L.V., Polke, J.M., Ling, H., MacDoanld, N.D., Tucci, A., Nanji, T., ...Revesz, T. (2015). Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism.. Neurobiol Aging, 36 (2), 1221.e1-1221.e6. doi:10.1016/j.neurobiolaging.2014.08.024
Stamelou, M., Bhatia, K.P. (2015). Atypical parkinsonism: diagnosis and treatment.. NEUROLOGIC CLINICS, 33 (1), 39-+. doi:10.1016/j.ncl.2014.09.012
Ganos, C., Müller-Vahl, K., Bhatia, K.P. (2015). Blocking Phenomena in Gilles de la Tourette Syndrome. Movement Disorders Clinical Practice, 2 (4), 438-439. doi:10.1002/mdc3.12199
Erro, R., Bhatia, K.P. (2015). Cardiac Risks and Guidance Regarding Domperidone: An Ounce of Prevention Is Worth a Pound of Cure. Movement Disorders Clinical Practice, 2 (4), 443-444. doi:10.1002/mdc3.12219
Hirschbichler, S.T., Erro, R., Batla, A., Bhatia, K.P. (2015). Classic PD-like rest tremor associated with the tau p.R406W mutation. PARKINSONISM & RELATED DISORDERS, 21 (8), 1002-1004. doi:10.1016/j.parkreldis.2015.05.012
Zandi, M.S., Paterson, R.W., Ellul, M.A., Jacobson, L., Al-Diwani, A., Jones, J.L., ...Bhatia, K.P. (2015). Clinical relevance of serum antibodies to extracellular N-methyl-D-aspartate receptor epitopes.. J. Neurol. Neurosurg. Psychiatr., 86 (7), 708-713.
Batla, A., Adams, M.E., Erro, R., Ganos, C., Balint, B., Mencacci, N.E., Bhatia, K.P. (2015). CORTICAL PENCIL LINING IN NEUROFERRITINOPATHY: A DIAGNOSTIC CLUE. NEUROLOGY, 84 (17), 1816-1818. doi:10.1212/WNL.0000000000001511
Comella, C.L., Fox, S.H., Bhatia, K.P., Perlmutter, J.S., Jinnah, H.A., Zurowski, M., ...Waliczek, T. (2015). Development of the Comprehensive Cervical Dystonia Rating Scale: Methodology. Movement Disorders Clinical Practice, 2 (2), 135-141. doi:10.1002/mdc3.12131
Kanovsky, P., Bhatia, K.P., Rosales, R.L. (2015). Dystonia and dystonic syndromes. .
Kanovsky, P., Rosales, R.L., Bhatia, K.P. (2015). Dystonia: The syndrome, its term, concept and their evolution. In Dystonia and Dystonic Syndromes. (pp. 3-12). .
Paudel, R., Li, A., Hardy, J., Bhatia, K.P., Houlden, H., Holton, J. (2015). DYT6 dystonia: A neuropathological study. Neurodegenerative Diseases, 16 (3-4), 273-278. doi:10.1159/000440863
Ganos, C., Pareés, I., Bhatia, K.P. (2015). Effort-Related Behaviors in Charcot's Lectures on Hysteria. Movement Disorders Clinical Practice, 2 (2), 201-202. doi:10.1002/mdc3.12152
Brugger, F., Jesus, S., Ganos, C., Bhatia, K.P. (2015). Episodic akinesia of jaw movements akin to freezing in multiple system atrophy. PARKINSONISM & RELATED DISORDERS, 21 (12), 1483-1484. doi:10.1016/j.parkreldis.2015.10.014
Praschberger, R., Balint, B., Mencacci, N.E., Hersheson, J., Rubio-Agusti, I., Kullmann, D.M., ...Houlden, H. (2015). Expanding the Phenotype and Genetic Defects Associated with the GOSR2 Gene. Movement Disorders Clinical Practice, 2 (3), 271-273. doi:10.1002/mdc3.12190
Ferre, E.R., Ganos, C., Bhatia, K.P., Haggard, P. (2015). Feedforward somatosensory inhibition is normal in cervical dystonia. PARKINSONISM & RELATED DISORDERS, 21 (3), 266-270. doi:10.1016/j.parkreldis.2014.12.026
Antelmi, E., Ferri, R., Iranzo, A., Arnulf, I., Dauvilliers, Y., Bhatia, K.P., ...Plazzi, G. (2015). From state dissociation to status dissociatus.. Sleep medicine reviews, 28 5-17. doi:10.1016/j.smrv.2015.07.003
Erro, R., Hersheson, J., Ganos, C., Mencacci, N.E., Stamelou, M., Batla, A., ...Hardy, J. (2015). H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?. Movement Disorders, 30 (6), 828-833. doi:10.1002/mds.26129
Erro, R., Hersheson, J., Ganos, C., Mencacci, N.E., Stamelou, M., Batla, A., ...Hardy, J. (2015). H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations?. MOVEMENT DISORDERS, 30 (6), 828-833. doi:10.1002/mds.26129
Balint, B., Bhatia, K.P. (2015). Hot topic: Recessive mutations in the a3(VI) collagen gene COL6A3 cause early-onset isolated dystonia. MOVEMENT DISORDERS, 30 (12), 1622. doi:10.1002/mds.26355
Heywood, W.E., Galimberti, D., Bliss, E., Sirka, E., Paterson, R.W., Magdalinou, N.K., ...Fenoglio, C. (2015). Identification of novel CSF biomarkers for neurodegeneration and their validation by a high-throughput multiplexed targeted proteomic assay. Molecular Neurodegeneration, 10 doi:10.1186/s13024-015-0059-y
Antelmi, E., Plazzi, G., Erro, R., Tinuper, P., Balint, B., Liguori, R., Bhatia, K.P. (2015). Intermittent head drops: the differential spectrum. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 87 (4), 414-419. doi:10.1136/jnnp-2015-310864
Balint, B., Bhatia, K.P. (2015). Isolated and combined dystonia syndromes - an update on new genes and their phenotypes. EUROPEAN JOURNAL OF NEUROLOGY, 22 (4), 610-617. doi:10.1111/ene.12650
Batla, A., Erro, R., Ganos, C., Stamelou, M., Bhatia, K.P. (2015). Levodopa-Responsive Parkinsonism with Prominent Freezing and Abnormal Dopamine Transporter Scan Associated with SANDO Syndrome. Movement Disorders Clinical Practice, 2 (3), 304-307. doi:10.1002/mdc3.12164
Kinghorn, K., Castillo, K., Li, L., Bartolome, F., Angelova, P., Pope, S., ...Hardy, J. (2015). Loss of PLA2G6 leads to elevated mitochondrial lipid peroxidation and mitochondrial dysfunction. Brain, doi:10.1093/brain/awv132
Charlesworth, G., Angelova, P.R., Bartolomé-Robledo, F., Ryten, M., Trabzuni, D., Stamelou, M., ...Wood, N.W. (2015). Mutations in HPCA cause autosomal-recessive primary isolated dystonia. American Journal of Human Genetics, 96 (4), 657-665. doi:10.1016/j.ajhg.2015.02.007
Balint, B., Bhatia, K.P. (2015). Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome. Movement Disorders Clinical Practice, 2 (3), 230-231. doi:10.1002/mdc3.12178
Paudel, R., Li, A., Wiethoff, S., Bandopadhyay, R., Bhatia, K., de Silva, R., ...Holton, J.L. (2015). Neuropathology of Beta-propeller protein associated neurodegeneration (BPAN): a new tauopathy. ACTA NEUROPATHOLOGICA COMMUNICATIONS, 3 doi:10.1186/s40478-015-0221-3
Balint, B., Erro, R., Stamelou, M., Brugger, F., Antelmi, E., Batla, A., ...Bhatia, K. (2015). NMDAR-antibodies in atypical corticobasal syndrome - New phenotype or (contributing) epiphenomenon?.
Antelmi, E., Stamelou, M., Liguori, R., Bhatia, K.P. (2015). Nonmotor Symptoms in Dopa-Responsive Dystonia. Movement Disorders Clinical Practice, 2 (4), 347-356. doi:10.1002/mdc3.12211
Ribeiro, A., Bhatia, K.P. (2015). Nosology and classification of dystonia. In Dystonia and Dystonic Syndromes. Springer.
Ganos, C., Erro, R., Mir, P., Lang, A.E., Bhatia, K.P., Vidailhet, M. (2015). On the long-term outcome of orthostatic tremor. PARKINSONISM & RELATED DISORDERS, 21 (10), 1290-1291. doi:10.1016/j.parkreldis.2015.07.023
Balint, B., Bhatia, K.P. (2015). Parkinsonism and Other Movement Disorders Associated with Chediak-Higashi Syndrome: Case Report and Systematic Literature Review. Movement Disorders Clinical Practice, 2 (1), 93-98. doi:10.1002/mdc3.12111
Erro, R., Bhatia, K.P., Tinazzi, M. (2015). Parkinsonism following neuroleptic exposure: A double-hit hypothesis?. MOVEMENT DISORDERS, 30 (6), 780-785. doi:10.1002/mds.26209
Erro, R., Stamelou, M., Bhatia, K.P. (2015). Paroxysmal dyskinesias. In Parkinson's Disease and Movement Disorders. Lww.
Antelmi, E., Erro, R., Pisani, A., Mencacci, N., Bhatia, K.P. (2015). Persistent chorea in DYT6, due to anticholinergic therapy. PARKINSONISM & RELATED DISORDERS, 21 (10), 1282-1283. doi:10.1016/j.parkreldis.2015.07.024
Ganos, C., Garrido, A., Navalpotro, I., Ricciardi, L., Martino, D., Edwards, M.J., ...Bhatia, K.P. (2015). Premonitory urge to tic in Tourette's is associated with interoceptive awareness.
Ganos, C., Garrido, A., Navalpotro-Gomez, I., Ricciardi, L., Martino, D., Edwards, M.J., ...Bhatia, K.P. (2015). Premonitory Urge to Tic in Tourette's Is Associated With Interoceptive Awareness. MOVEMENT DISORDERS, 30 (9), 1198-1202. doi:10.1002/mds.26228
Erro, R., Ciocca, M., Hirschbichler, S.T., Rothwell, J.C., Bhatia, K.P. (2015). Primary writing tremor is a dystonic trait: Evidence from an instructive family. JOURNAL OF THE NEUROLOGICAL SCIENCES, 356 (1-2), 210-211. doi:10.1016/j.jns.2015.06.040
Kojovic, M., Bologna, M., Edwards, M.J., Rothwell, J.C., Bhatia, K.P. (2015). Reply to Letter: Transcranial Magnetic Stimulation for Parkinson's Disease. MOVEMENT DISORDERS, 30 (14), 1973-1974. doi:10.1002/mds.26441
Mencacci, N.E., Pittman, A.M., Isaias, I.U., Hardy, J., Klebe, S., Bhatia, K.P., Wood, N.W. (2015). Reply: Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.. Brain, 138 (5), e352. doi:10.1093/brain/awu309
Ganos, C., Kassavetis, P., Cerdan, M., Erro, R., Balint, B., Price, G., ...Bhatia, K.P. (2015). Revisiting the Syndrome of “Obsessional Slowness”. Movement Disorders Clinical Practice, 2 (2), 163-169. doi:10.1002/mdc3.12140
Manohar, S.G., Chong, T.T.J., Apps, M.A.J., Batla, A., Stamelou, M., Jarman, P.R., ...Husain, M. (2015). Reward Pays the Cost of Noise Reduction in Motor and Cognitive Control. Current Biology, 25 (13), 1707-1716. doi:10.1016/j.cub.2015.05.038
Manohar, S.G., Chong, T.T.-.J., Apps, M.A.J., Batla, A., Stamelou, M., Jarman, P.R., ...Husain, M. (2015). Reward Pays the Cost of Noise Reduction in Motor and Cognitive Control. CURRENT BIOLOGY, 25 (13), 1707-1716. doi:10.1016/j.cub.2015.05.038
Ganos, C., Hersheson, J., Adams, M., Bhatia, K.P., Houlden, H. (2015). Syndromic associations and RNF216 mutations. PARKINSONISM & RELATED DISORDERS, 21 (11), 1389-1390. doi:10.1016/j.parkreldis.2015.09.010
Ganos, C., Hersheson, J., Adams, M., Bhatia, K.P., Houlden, H. (2015). The 4H syndrome due to RNF216 mutation. PARKINSONISM & RELATED DISORDERS, 21 (9), 1122-1123. doi:10.1016/j.parkreldis.2015.07.012
Ganos, C., Hersheson, J., Adams, M., Bhatia, K.P., Houlden, H. (2015). The 4H syndrome due to RNF216 mutation. Parkinsonism and Related Disorders, 21 (9), 1122-1123. doi:10.1016/j.parkreldis.2015.07.012
Schottlaender, L.V., Polke, J.M., Ling, H., MacDoanld, N.D., Tucci, A., Nanji, T., ...Revesz, T. (2015). The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism. Neurobiology of Aging, 36 (2), 1221.e1-1221.e6. doi:10.1016/j.neurobiolaging.2014.08.024
Schottlaender, L.V., Polke, J.M., Ling, H., MacDoanld, N.D., Tucci, A., Nanji, T., ...Revesz, T. (2015). The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism (vol 36, 1221.e1, 2015). NEUROBIOLOGY OF AGING, 36 (4), 1768. doi:10.1016/j.neurobiolaging.2015.02.027
Mencacci, N.E., R'bibo, L., Bandres-Ciga, S., Carecchio, M., Zorzi, G., Nardocci, N., ...Pittman, A.M. (2015). The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort. Human Molecular Genetics, 24 (18), 5326-5329. doi:10.1093/hmg/ddv255
Gardiner, A.R., Jaffer, F., Dale, R.C., Labrum, R., Erro, R., Meyer, E., ...Kullmann, D. (2015). The clinical and genetic heterogeneity of paroxysmal dyskinesias. Brain, 138 (Pt 12), 3567-3580. doi:10.1093/brain/awv310
Stamelou, M., Diehl-Schmid, J., Hapfelmeier, A., Kontaxopoulou, D., Stefanis, L., Oertel, W.H., ...Hoeglinger, G.U. (2015). The frontal assessment battery is not useful to discriminate progressive supranuclear palsy from frontotemporal dementias. PARKINSONISM & RELATED DISORDERS, 21 (10), 1264-1268. doi:10.1016/j.parkreldis.2015.08.006
Batla, A., Sanchez, M.C., Erro, R., Ganos, C., Stamelou, M., Balint, B., ...Bhatia, K.P. (2015). The role of cerebellum in patients with late onset cervical/segmental dystonia?-Evidence from the clinic. PARKINSONISM & RELATED DISORDERS, 21 (11), 1317-1322. doi:10.1016/j.parkreldis.2015.09.013
Kojovic, M., Kassavetis, P., Bologna, M., Parees, I., Rubio-Agusti, I., Beraredelli, A., ...Bhatia, K.P. (2015). Transcranial magnetic stimulation follow-up study in early Parkinson's disease: A decline in compensation with disease progression?. MOVEMENT DISORDERS, 30 (8), 1098-1106. doi:10.1002/mds.26167
Saifee, T.A., Parees, I., Kassavetis, P., Kaski, D., Bronstein, A.M., Rothwell, J.C., ...Teo, J.T. (2015). Tremor in Charcot-Marie-Tooth disease: No evidence of cerebellar dysfunction. CLINICAL NEUROPHYSIOLOGY, 126 (9), 1817-1824. doi:10.1016/j.clinph.2014.12.023
Brugger, F., Erro, R., Balint, B., Kägi, G., Barone, P., Bhatia, K.P. (2015). Why is there motor deterioration in Parkinson's disease during systemic infections-a hypothetical view.. NPJ Parkinson's disease, 1 15014-. doi:10.1038/npjparkd.2015.14

2014

Kara, E., Kiely, A.P., Proukakis, C., Giffin, N., Love, S., Hehir, J., ...Nacheva, E. (2014). A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.. JAMA NEUROLOGY, 71 (9), 1162-1171. doi:10.1001/jamaneurol.2014.994
Kara, E., Kiely, A., Proukakis, C., Giffin, N., Love, S., Hehir, J., ...Nacheva, E. (2014). A 6.4MB duplication of the alpha-synuclein locus causing frontotemporal dementia and Parkinsonism - phenotype-genotype correlations.
Batla, A., Bhatia, K.P. (2014). A new gene for Fahr's syndrome-PDGF-B.. MOVEMENT DISORDERS, 29 (3), 307. doi:10.1002/mds.25788
Veneziano, L., Parkinson, M.H., Mantuano, E., Frontali, M., Bhatia, K.P., Giunti, P. (2014). A Novel De Novo Mutation of the TITF1/NKX2-1 Gene Causing Ataxia, Benign Hereditary Chorea, Hypothyroidism and a Pituitary Mass in a UK Family and Review of the Literature. Cerebellum, 13 (5), 588-595. doi:10.1007/s12311-014-0570-7
Veneziano, L., Parkinson, M.H., Mantuano, E., Frontali, M., Bhatia, K.P., Giunti, P. (2014). A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.. Cerebellum, 13 (5), 588-595. doi:10.1007/s12311-014-0570-7
Sadnicka, A., Hamada, M., Bhatia, K., Rothwell, J., Mark, E. (2014). A REFLECTION ON PLASTICITY RESEARCH IN WRITING DYSTONIA.
Sadnicka, A., Hamada, M., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2014). A reflection on plasticity research in writing dystonia.
Sadnicka, A., Hamada, M., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2014). A reflection on plasticity research in writing dystonia.
Sadnicka, A., Hamada, M., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2014). A reflection on plasticity research in writing dystonia.
Sadnicka, A., Hamada, M., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2014). A Reflection on Plasticity Research in Writing Dystonia. MOVEMENT DISORDERS, 29 (8), 980-987. doi:10.1002/mds.25908
Sadnicka, A., Hamada, M., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2014). A reflection on plasticity research in writing dystonia.. MOVEMENT DISORDERS, 29 (8), 980-987. doi:10.1002/mds.25908
Erro, R., Martino, D., Ganos, C., Damasio, J., Batla, A., Bhatia, K.P. (2014). Adult-Onset Primary Dystonic Tics: A Different Entity?. Movement Disorders Clinical Practice, 1 (1), 62-66. doi:10.1002/mdc3.12005
Sadnicka, A., Teo, J., Kojovic, M., Parees, I., Saifee, T.A., Panagiotis, K., ...Edwards, M.J. (2014). All in the blink of any eye: insights into the pathophysiology of DYT1 and DYT6 dystonia.
Sadnicka, A., Teo, J., Kojovic, M., Parees, I., Saifee, T.A., Panagiotis, K., ...Edwards, M.J. (2014). All in the blink of any eye: insights into the pathophysiology of DYT1 and DYT6 dystonia.
Sadnicka, A., Teo, J.T., Kojovic, M., Parees, I., Saifee, T., Kassavetis, P., ...Edwards, M.J. (2014). All in the blink of any eye: Insights into the pathophysiology of DYT1 and DYT6 dystonia.
Sheerin, U.-.M., Schneider, S.A., Carr, L., Deuschl, G., Hopfner, F., Stamelou, M., ...Bhatia, K.P. (2014). ALS2 mutations: juvenile amyotrophic lateral sclerosis and generalized dystonia.. Neurology, 82 (12), 1065-1067. doi:10.1212/WNL.0000000000000254
Batla, A., Cerdan, M., Ganos, C., Erro, R., Stamelou, M., Bhatia, K.P. (2014). Cerebellar abnormalities in clinical practice of dystonia.
Batla, A., Cerdan, M., Ganos, C., Erro, R., Stamelou, M., Bhatia, K.P. (2014). Cerebellar abnormalities in clinical practice of dystonia.
Sadnicka, A., Hamada, M., Bhatia, K.P., Rothwell, J.C., Edwards, M.J. (2014). Cerebellar stimulation fails to modulate motor cortex plasticity in writing dystonia.. MOVEMENT DISORDERS, 29 (10), 1304-1307. doi:10.1002/mds.25881
Petrović, I.N., Kresojević, N., Ganos, C., Svetel, M., Dragašević, N., Bhatia, K.P., Kostić, V.S. (2014). Characteristic “Forcible” Geste Antagoniste in Oromandibular Dystonia Resulting From Pantothenate Kinase-Associated Neurodegeneration. Movement Disorders Clinical Practice, 1 (2), 112-114. doi:10.1002/mdc3.12035
Stamelou, M., Sheerin, U.M., Wood, N., Bhatia, K.P. (2014). Clinical/scientific notes: The entity of parkinsonism and associated lipomatosis. Neurology, 83 (18), 1673-1674. doi:10.1212/wnl.0000000000000937
De Pablo-Fernandez, E., Doherty, K.M., Holton, J.L., Revesz, T., Djamshidian, A., Limousin, P., ...Ling, H. (2014). Concomitant fragile X-associated tremor ataxia syndrome and Parkinson's disease: a clinicopathological report of two cases.. J Neurol Neurosurg Psychiatry, doi:10.1136/jnnp-2014-309460
Parees, I., Sadnicka, A., Wijesekera, L., Edwards, M.J., Bhatia, K.P., Cordivari, C. (2014). Cortical myclonus: A case series.
Stamelou, M., Bhatia, K. (2014). Dementia in Parkinson's disease and atypical parkinsonism. In Movement Disorders in Dementias. (pp. 179-197). .
Brigo, F., Erro, R., Marangi, A., Bhatia, K., Tinazzi, M. (2014). Differentiating drug-induced parkinsonism from Parkinson's disease: an update on non-motor symptoms and investigations.. PARKINSONISM & RELATED DISORDERS, 20 (8), 808-814. doi:10.1016/j.parkreldis.2014.05.011
Butt, S., Leung, R.S., Batla, A., Bhatia, K., Raeburn, A.J., Zarate, N., Emmanuel, A. (2014). Dysmotility in Parkinson's Disease Correlates to Gut Symptoms: Findings of a Wireless Motility Capsule Study.
Butt, S.K., Leung, R., Bala, A., Bhatia, K., Raeburn, A., Emmanuel, A. (2014). DYSMOTILITY IN PARKINSON'S DISEASE CORRELATES TO GUT SYMPTOMS: FINDINGS OF A WIRELESS MOTILITY CAPSULE STUDY.
Albanese, A., Bhatia, K., Bressman, S.B., DeLong, M.R., Fahn, S., Fung, V.S.C., ...Klein, C. (2014). Dystonia after severe brain injuries. MOVEMENT DISORDERS, 29 (4), 578. doi:10.1002/mds.25840
Ganos, C., Biskup, S., Krüger, S., Meyer-Osores, A., Hodecker, S., Hagel, C., ...Münchau, A. (2014). Dystonia with aphonia, slow horizontal saccades, epilepsy and photic myoclonus: a novel syndrome?. PARKINSONISM & RELATED DISORDERS, 20 (3), 328-331. doi:10.1016/j.parkreldis.2013.11.011
Balint, B., Bhatia, K.P. (2014). Dystonia: an update on phenomenology, classification, pathogenesis and treatment.. CURRENT OPINION IN NEUROLOGY, 27 (4), 468-476. doi:10.1097/WCO.0000000000000114
Ganos, C., Saifee, T.A., Kassavetis, P., Erro, R., Batla, A., Cordivari, C., Bhatia, K.P. (2014). Dystonic Tremor and Spasmodic Dysphonia in Spinocerebellar Ataxia Type 12. Movement Disorders Clinical Practice, 1 (1), 79-81. doi:10.1002/mdc3.12006
Bhatia, K.P. (2014). Erratum: "That DAT" gene that causes dystonia-parkinsonism: broadening the phenotype (Brain 2014) 137 (976-77) Doi:10.1093/brain/awu056). Brain, 137 (8), doi:10.1093/brain/awu170
Batla, A., Cerdan, M., Ganos, C., Stamelou, M., Erro, R., Bhatia, K.P. (2014). Evidence of cerebellar abnormalities in large cohort of cervical segmental dystonia.
Erro, R., Stamelou, M., Saifee, T.A., Ganos, C., Antelmi, E., Balint, B., ...Bhatia, K.P. (2014). Facial tremor in dystonia.. PARKINSONISM & RELATED DISORDERS, 20 (8), 924-925. doi:10.1016/j.parkreldis.2014.04.029
Erro, R., Cordivari, C., Catania, S., Bhatia, K.P., Edwards, M.J. (2014). Fixed Dystonia of the Tongue. Movement Disorders Clinical Practice, 1 (2), 134-135. doi:10.1002/mdc3.12026
Damásio, J., Taipa, R., Melo-Pires, M., Guimarães, A., Bhatia, K.P., Santos, M., Carrilho, I. (2014). Freezing of gait--first motor manifestation in late infantile variant neuronal ceroid lipofuscinosis.. PARKINSONISM & RELATED DISORDERS, 20 (2), 243-244. doi:10.1016/j.parkreldis.2013.10.015
Balint, B., Bhatia, K.P. (2014). Friend or foe? IgLON5 antibodies in a novel tauopathy with prominent sleep movement disorder, ataxia, and chorea.. MOVEMENT DISORDERS, 29 (8), 989. doi:10.1002/mds.25926
Merello, M., Bhatia, K. (2014). From the Reflex Hammer to Molecular Biology: Do Clinical Descriptions Still Play a Role in Our Neurological Decision Making? Jorge Luis Borges and the Analytic Language of Wilkins. Movement Disorders Clinical Practice, 1 (1), 1-2. doi:10.1002/mdc3.12010
Ganos, C., Erro, R., Cavanna, A.E., Bhatia, K.P. (2014). Functional tics and echophenomena.. PARKINSONISM & RELATED DISORDERS, 20 (12), 1440-1441. doi:10.1016/j.parkreldis.2014.10.001
Edwards, M.J., Stone, J., Lang, A.E. (2014). Functional/psychogenic movement disorders: do we know what they are?. MOVEMENT DISORDERS, 29 (13), 1696-1697. doi:10.1002/mds.26038
Nalls, M.A., Saad, M., Noyce, A.J., Keller, M.F., Schrag, A., Bestwick, J.P., ...Cookson, M.R. (2014). Genetic comorbidities in Parkinson's disease. HUMAN MOLECULAR GENETICS, 23 (3), 831-841. doi:10.1093/hmg/ddt465
Mok, K.Y., Schneider, S.A., Trabzuni, D., Stamelou, M., Edwards, M., Kasperaviciute, D., ...Bhatia, K.P. (2014). Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel. Movement Disorders, 29 (2), 245-251. doi:10.1002/mds.25732
Mok, K.Y., Schneider, S.A., Trabzuni, D., Stamelou, M., Edwards, M., Kasperaviciute, D., ...Bhatia, K.P. (2014). Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel.. Mov Disord, 29 (2), 245-251. doi:10.1002/mds.25732
Erro, R., Bhatia, K.P., Hardy, J. (2014). GNAL mutations and dystonia.. JAMA NEUROLOGY, 71 (8), 1052-1053. doi:10.1001/jamaneurol.2014.1506
Saifee, T.A., Ganos, C., Kassavetis, P., Erro, R., Batla, A., Cordivari, C., Bhatia, K.P. (2014). Is tremor in SCA12 dystonic?.
Nalls, M.A., Pankratz, N., Lill, C.M., Do, C.B., Hernandez, D.G., Saad, M., ...Sharma, M. (2014). Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. NATURE GENETICS, 46 (9), 989-+. doi:10.1038/ng.3043
Kefalopoulou, Z., Politis, M., Piccini, P., Mencacci, N., Bhatia, K., Jahanshahi, M., ...Björklund, A. (2014). Long-term clinical outcome of fetal cell transplantation for Parkinson disease: two case reports.. JAMA NEUROLOGY, 71 (1), 83-87. doi:10.1001/jamaneurol.2013.4749
Pareés, I., Brown, H., Nuruki, A., Adams, R.A., Davare, M., Bhatia, K.P., ...Edwards, M.J. (2014). Loss of sensory attenuation in patients with functional (psychogenic) movement disorders.. BRAIN, 137 2916-2921. doi:10.1093/brain/awu237
Birsa, N., Norkett, R., Wauer, T., Mevissen, T.E.T., Wu, H.-.C., Foltynie, T., ...Plun-Favreau, H. (2014). Lysine 27 ubiquitination of the mitochondrial transport protein Miro is dependent on serine 65 of the Parkin ubiquitin ligase.. J Biol Chem, 289 (21), 14569-14582. doi:10.1074/jbc.M114.563031
Bhatia, K., Merello, M. (2014). MDCP: The First Year Bygone - Editors' Note to the Readership. Movement Disorders Clinical Practice, 1 (4), 275-. doi:10.1002/mdc3.12108
Kojovic, M., Mir, P., Trender-Gerhard, I., Schneider, S.A., Pareés, I., Edwards, M.J., ...Jahanshahi, M. (2014). Motivational modulation of bradykinesia in Parkinson's disease off and on dopaminergic medication.. J Neurol, 261 (6), 1080-1089. doi:10.1007/s00415-014-7315-x
Katschnig-Winter, P., Schwingenschuh, P., Davare, M., Sadnicka, A., Rothwell, J.C., Bhatia, K.P., ...Schmidt, R. (2014). Motor sequence learning and motor adaptation in primary cervical dystonia. JOURNAL OF CLINICAL NEUROSCIENCE, 21 (6), 934-938. doi:10.1016/j.jocn.2013.08.019
Katschnig-Winter, P., Schwingenschuh, P., Davare, M., Sadnicka, A., Schmidt, R., Rothwell, J.C., ...Edwards, M.J. (2014). Motor sequence learning and motor adaptation in primary cervical dystonia. Journal of Clinical Neuroscience, 21 (6), 934-938. doi:10.1016/j.jocn.2013.08.019
Bhatia, K.P., Carrechio, M., Schneider, S. (2014). Movement disorders in metabolic disease in adulthood. In Movement Disorders in Neurologic and Systemic Disease. Cambridge University Press.
Paudel, R., Kiely, A., Li, A., Lashley, T., Bandopadhyay, R., Hardy, J., ...Holton, J.L. (2014). Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions.. Acta Neuropathol Commun, 2 (1), doi:10.1186/s40478-014-0159-x
Charlesworth, G., Bhatia, K.P., Wood, N.W. (2014). No pathogenic GNAL mutations in 192 sporadic and familial cases of cervical dystonia. Movement Disorders, 29 (1), 154-155. doi:10.1002/mds.25713
Charlesworth, G., Bhatia, K.P., Wood, N.W. (2014). No pathogenic GNAL mutations in 192 sporadic and familial cases of cervical dystonia.. Mov Disord, 29 (1), 154-155. doi:10.1002/mds.25713
Batla, A., Smith, M., Seth, J., Hofereiter, J., Bhatia, K.P., Panicker, J.N. (2014). Nocturnal polyuria in patients with Parkinson's disease reporting nocturia.
Sadnicka, A., Patani, B., Saifee, T., Parees, I., Kassavetis, P., Bhatia, K.P., ...Edwards, M.J. (2014). Normal adaptation in cervical dystonia: A fundamental cerebellar computation is intact.
Sadnicka, A., Patani, B., Saifee, T., Kassavetis, P., Parees, I., Korlipari, P., ...Edwards, M. (2014). NORMAL MOTOR ADAPTATION IN CERVICAL DYSTONIA: A FUNDAMENTAL CEREBELLAR COMPUTATION IS INTACT.
Sadnicka, A., Patani, B., Saifee, T.A., Kassavetis, P., Pareés, I., Korlipara, P., ...Edwards, M.J. (2014). Normal Motor Adaptation in Cervical Dystonia: A Fundamental Cerebellar Computation is Intact. Cerebellum, 13 (5), 558-567. doi:10.1007/s12311-014-0569-0
Sadnicka, A., Patani, B., Saifee, T.A., Kassavetis, P., Pareés, I., Korlipara, P., ...Edwards, M.J. (2014). Normal motor adaptation in cervical dystonia: a fundamental cerebellar computation is intact.. Cerebellum, 13 (5), 558-567. doi:10.1007/s12311-014-0569-0
Volkmann, J., Mueller, J., Deuschl, G., Kühn, A.A., Krauss, J.K., Poewe, W., ...Kivi, A. (2014). Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial.. LANCET NEUROLOGY, 13 (9), 875-884. doi:10.1016/S1474-4422(14)70143-7
Jahanshahi, M., Torkamani, M., Beigi, M., Wilkinson, L., Page, D., Madeley, L., ...Limousin, P. (2014). Pallidal stimulation for primary generalised dystonia: Effect on cognition, mood and quality of life. Journal of Neurology, 261 (1), 164-173. doi:10.1007/s00415-013-7161-2
Jahanshahi, M., Torkamani, M., Beigi, M., Wilkinson, L., Page, D., Madeley, L., ...Limousin, P. (2014). Pallidal stimulation for primary generalised dystonia: effect on cognition, mood and quality of life.. J Neurol, 261 (1), 164-173. doi:10.1007/s00415-013-7161-2
Mencacci, N.E., Isaias, I.U., Reich, M.M., Ganos, C., Plagnol, V., Polke, J.M., ...Pittman, A.M. (2014). Parkinson's disease in GTP cyclohydrolase 1 mutation carriers. BRAIN, 137 2480-2492. doi:10.1093/brain/awu179
Mencacci, N.E., Isaias, I.U., Reich, M.M., Ganos, C., Plagnol, V., Polke, J.M., ...Pittman, A.M. (2014). Parkinson's disease in GTP cyclohydrolase 1 mutation carriers.. Brain, 137 (9), 2480-2492. doi:10.1093/brain/awu179
Erro, R., Sheerin, U.-.M., Bhatia, K.P. (2014). Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification.. MOVEMENT DISORDERS, 29 (9), 1108-1116. doi:10.1002/mds.25933
Baschieri, F., Batla, A., Erro, R., Ganos, C., Cordivari, C., Bhatia, K.P. (2014). Paroxysmal exercise-induced dystonia due to GLUT1 mutation can be responsive to levodopa: a case report. JOURNAL OF NEUROLOGY, 261 (3), 615-616. doi:10.1007/s00415-014-7250-x
Ganos, C., Mencacci, N., Gardiner, A., Erro, R., Batla, A., Houlden, H., Bhatia, K.P. (2014). Paroxysmal Kinesigenic Dyskinesia May Be Misdiagnosed in Co-occurring Gilles de la Tourette Syndrome. Movement Disorders Clinical Practice, 1 (1), 84-86. doi:10.1002/mdc3.12001
Batla, A., Erro, R., Stamelou, M., Schneider, S.A., Schwingenschuh, P., Ganos, C., Bhatia, K.P. (2014). Patients with scans without evidence of dopaminergic deficit: a long-term follow-up study.. MOVEMENT DISORDERS, 29 (14), 1820-1825. doi:10.1002/mds.26018
Pareés, I., Kojovic, M., Pires, C., Rubio-Agusti, I., Saifee, T.A., Sadnicka, A., ...Carson, A. (2014). Physical precipitating factors in functional movement disorders. Journal of the Neurological Sciences, 338 (1-2), 174-177. doi:10.1016/j.jns.2013.12.046
Pareés, I., Kojovic, M., Pires, C., Rubio-Agusti, I., Saifee, T.A., Sadnicka, A., ...Carson, A. (2014). Physical precipitating factors in functional movement disorders.. JOURNAL OF THE NEUROLOGICAL SCIENCES, 338 (1-2), 174-177. doi:10.1016/j.jns.2013.12.046
van der Salm, S.M.A., Erro, R., Cordivari, C., Edwards, M.J., Koelman, J.H.T.M., van den Ende, T., ...Tijssen, M.A.J. (2014). Propriospinal myoclonus: clinical reappraisal and review of literature.. NEUROLOGY, 83 (20), 1862-1870. doi:10.1212/WNL.0000000000000982
Erro, R., Edwards, M.J., Bhatia, K.P., Esposito, M., Farmer, S.F., Cordivari, C. (2014). Psychogenic axial myoclonus: clinical features and long-term outcome.. PARKINSONISM & RELATED DISORDERS, 20 (6), 596-599. doi:10.1016/j.parkreldis.2014.02.026
Balint, B., van Winsen, L.M.L., Bhatia, K.P., Bloem, B.R. (2014). Psychogenic Movement Disorders: Gait Is a Give-Away!. Movement Disorders Clinical Practice, 1 (2), 110-111. doi:10.1002/mdc3.12031
Ganos, C., Aguirregomozcorta, M., Batla, A., Stamelou, M., Schwingenschuh, P., Münchau, A., ...Bhatia, K.P. (2014). Psychogenic paroxysmal movement disorders - Clinical features anddiagnostic clues. Parkinsonism and Related Disorders, 20 (1), 41-46. doi:10.1016/j.parkreldis.2013.09.012
Ganos, C., Aguirregomozcorta, M., Batla, A., Stamelou, M., Schwingenschuh, P., Münchau, A., ...Bhatia, K.P. (2014). Psychogenic paroxysmal movement disorders--clinical features and diagnostic clues.. PARKINSONISM & RELATED DISORDERS, 20 (1), 41-46. doi:10.1016/j.parkreldis.2013.09.012
Ganos, C., Edwards, M., Bhatia, K.P. (2014). Reply to R. Erro and M. Tinazzi's "Functional (psychogenic) paroxysms: the diagnosis is in the eye of the beholder".. PARKINSONISM & RELATED DISORDERS, 20 (3), 345. doi:10.1016/j.parkreldis.2013.11.015
Albanese, A., Bhatia, K., Bressman, S.B., DeLong, M.R., Fahn, S., Fung, V.S.C., ...Klein, C. (2014). Reply: Dystonia after severe head injuries. Movement Disorders, 29 (4), 578-579. doi:10.1002/mds.25861
Macerollo, A., Mencacci, N.E., Erro, R., Cordivari, C., Edwards, M.J., Wood, N.W., Bhatia, K.P. (2014). Screening of mutations in NOL3 in a myoclonic syndromes series.. J Neurol, 261 (9), 1830-1831. doi:10.1007/s00415-014-7463-z
Erro, R., Bhatia, K.P., Cordivari, C. (2014). Shaking on Standing: A Critical Review. Movement Disorders Clinical Practice, 1 (3), 173-179. doi:10.1002/mdc3.12053
Erro, R., Cordivari, C., Bhatia, K.P. (2014). SPG31 presenting with orthostatic tremor.. EUROPEAN JOURNAL OF NEUROLOGY, 21 (4), E34-E35. doi:10.1111/ene.12360
Dong, J., Gao, J., Nalls, M., Gao, X., Huang, X., Han, J., ...Chen, H. (2014). Susceptibility loci for pigmentation and melanoma in relation to Parkinson's disease. NEUROBIOLOGY OF AGING, 35 (6), doi:10.1016/j.neurobiolaging.2013.12.020
Macerollo, A., Perry, R., Stamelou, M., Batla, A., Mazumder, A.A., Adams, M.E., Bhatia, K.P. (2014). Susceptibility-weighted imaging changes suggesting brain iron accumulation in Huntington's disease: an epiphenomenon which causes diagnostic difficulty. EUROPEAN JOURNAL OF NEUROLOGY, 21 (2), E16-E17. doi:10.1111/ene.12298
Bhatia, K.P. (2014). 'That DAT' gene that causes dystonia-parkinsonism: broadening the phenotype.. BRAIN, 137 976-977. doi:10.1093/brain/awu056
Ganos, C., Taiwo, L., Stamelou, M., Batla, A., Erro, R., Bhatia, K.P. (2014). The clinical syndrome of dystonia with aphonia.
Erro, R., Stamelou, M., Ganos, C., Batla, A., Bhatia, K. (2014). The clinical syndrome of paroxysmal exercise-induced dystonia: Diagnostic outcomes and an algorithm.
Erro, R., Stamelou, M., Ganos, C., Skorvanek, M., Han, V., Batla, A., Bhatia, K.P. (2014). The Clinical Syndrome of Paroxysmal Exercise-Induced Dystonia: Diagnostic Outcomes and an Algorithm. Movement Disorders Clinical Practice, 1 (1), 57-61. doi:10.1002/mdc3.12007
Stamelou, M., Sheerin, U.-.M., Wood, N., Bhatia, K.P. (2014). The entity of parkinsonism and associated lipomatosis.. NEUROLOGY, 83 (18), 1673-1674. doi:10.1212/WNL.0000000000000937
Obeso, J.A., Rodriguez-Oroz, M.C., Stamelou, M., Bhatia, K.P., Burn, D.J. (2014). The expanding universe of disorders of the basal ganglia.. LANCET, 384 (9942), 523-531. doi:10.1016/S0140-6736(13)62418-6
Stamelou, M., Diehl-Schmidt, J., Kontaxopoulou, D., Hapfelmeier, A., Bhatia, K., Oertel, W., ...Hoeglinger, G. (2014). The FAB fails to discriminate PSP from FTD and to capture disease progression in frontal disorders.
Stamelou, M., Diehl-Schmidt, J., Kontaxopoulou, D., Hapfelmeier, A., Bhatia, K., Oertel, W., ...Hoeglinger, G. (2014). The FAB fails to discriminate PSP from FTD and to capture disease progression in frontal disorders.
Esposito, M., Erro, R., Edwards, M.J., Bhatia, K.P., Cawley, N., Choi, D., Cordivari, C. (2014). The pathophysiology of symptomatic propriospinal myoclonus. MOVEMENT DISORDERS, 29 (9), 1097-1099. doi:10.1002/mds.25951
Ganos, C., Edwards, M.J., Bhatia, K.P. (2014). The Phenomenology of Functional (Psychogenic) Dystonia. Movement Disorders Clinical Practice, 1 (1), 36-44. doi:10.1002/mdc3.12013
Stamelou, M., Charlesworth, G., Cordivari, C., Schneider, S.A., Kägi, G., Sheerin, U.M., ...Wood, N.W. (2014). The phenotypic spectrum of DYT24 due to ANO3 mutations. Movement Disorders, 29 (7), 928-934. doi:10.1002/mds.25802
Stamelou, M., Charlesworth, G., Cordivari, C., Schneider, S.A., Kägi, G., Sheerin, U.-.M., ...Wood, N.W. (2014). The phenotypic spectrum of DYT24 due to ANO3 mutations.. Mov Disord, 29 (7), 928-934. doi:10.1002/mds.25802
Ganos, C., Kassavetis, P., Erro, R., Edwards, M.J., Rothwell, J., Bhatia, K.P. (2014). The role of the cerebellum in the pathogenesis of cortical myoclonus.. MOVEMENT DISORDERS, 29 (4), 437-443. doi:10.1002/mds.25867
Ganos, C., Münchau, A., Bhatia, K.P. (2014). The Semiology of Tics, Tourette's, and Their Associations. Movement Disorders Clinical Practice, 1 (3), 145-153. doi:10.1002/mdc3.12043
Beilina, A., Rudenko, I.N., Kaganovich, A., Civiero, L., Chau, H., Kalia, S.K., ...Ndukwe, K. (2014). Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 111 (7), 2626-2631. doi:10.1073/pnas.1318306111
Macerollo, A., Batla, A., Kassavetis, P., Parees, I., Bhatia, K.P., Edwards, M.J. (2014). Using Reaction Time and Co-contraction to Differentiate Acquired (Secondary) from Functional “Fixed” Dystonia. Journal of Neurology, Neurosurgery and Psychiatry, 86 (8), doi:10.1136/jnnp-2014-309040
Schwingenschuh, P., Saifee, T.A., Katschnig-Winter, P., Koegl-Wallner, M., Macerollo, A., Culea, V., ...Werner, U. (2014). Validation of "laboratory-supported'' criteria for functional tremor.
Schwingenschuh, P., Saifee, T.A., Katschnig-Winter, P., Koegl-Wallner, M., Macerollo, A., Culea, V., ...Werner, U. (2014). Validation of "laboratory-supported" criteria for functional tremor.
Schwingenschuh, P., Saifee, T.A., Katschnig-Winter, P., Koegl-Wallner, M., Macerollo, A., Culea, V., ...Werner, U. (2014). Validation of "laboratory-supported" criteria for functional tremor.
Kefalopoulou, Z., Politis, M., Piccini, P., Mencacci, N., Bhatia, K., Jahanshahi, M., ...Bjoerklund, A. (2014). Very long-term clinical outcome of fetal cell transplantation for Parkinson's disease.

2013

Stamelou, M., Quinn, N.P., Bhatia, K.P. (2013). "Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.. MOVEMENT DISORDERS, 28 (9), 1184-1199. doi:10.1002/mds.25509
Filipovic, S.R., Bhatia, K.P., Rothwell, J.C. (2013). 1-Hz repetitive transcranial magnetic stimulation and diphasic dyskinesia in Parkinson's disease. MOVEMENT DISORDERS, 28 (2), 245-246. doi:10.1002/mds.25261
Mencacci, N., Pittman, A., Sheerin, U., Charlesworth, G., Hughes, D., Sweeney, M., ...Bhatia, K. (2013). A comprehensive diagnostic test for familial and early onset Parkinson's disease based on next-generation sequencing. MOVEMENT DISORDERS, 28 S408.
Holmans, P., Moskvina, V., Jones, L., Sharma, M., Vedernikov, A., Buchel, F., ...Nicolaou, N. (2013). A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Hum.Mol.Genet., 22 (5), 1039-1049. doi:10.1093/hmg/dds492
Comella, C., Bhatia, K. (2013). An international survey of patients with cervical dystonia.
Moskvina, V., Harold, D., Russo, G., Vedemikov, A., Sharma, M., Saad, M., ...Keller, M.F. (2013). Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk. JAMA NEUROLOGY, 70 (10), 1268-1276. doi:10.1001/jamaneurol.2013.448
Charlesworth, G., Plagnol, V., Holmstroem, K.M., Bras, J., Sheerin, U.M., Preza, E., ...Stamelou, M. (2013). ANO3-A novel cause of primary dystonia.
Fung, V.S.C., Jinnah, H.A., Bhatia, K., Vidailhet, M. (2013). Assessment of patients with isolated or combined dystonia: An update on dystonia syndromes. MOVEMENT DISORDERS, 28 (7), 889-898. doi:10.1002/mds.25549
Charlesworth, G., Mohire, M.D., Schneider, S.A., Stamelou, M., Wood, N.W., Bhatia, K.P. (2013). Ataxia telangiectasia presenting as dopa-responsive cervical dystonia.. NEUROLOGY, 81 (13), 1148-1151. doi:10.1212/WNL.0b013e3182a55fa2
Stamelou, M., Quinn, N.P., Bhatia, K.P. (2013). 'Atypical' atypical parkinsonism: New genetic conditions presenting with features of PSP, CBD or MSA: A diagnostic guide.
Macerollo, A., Batla, A., Stamelou, M., Bhatia, K. (2013). Brain iron accumulation in juvenile Huntington's disease.
Macerollo, A., Batla, A., Stamelou, M., Bhatia, K. (2013). Brain iron accumulation in juvenile Huntington's disease. JOURNAL OF NEUROLOGY, 260 S192.
Pauls, K.A.M., Krauss, J.K., Kaempfer, C.E., Schrader, C., Suedmeyer, M., Allert, N., ...Fogel, W. (2013). Causes of therapeutic failure of pallidal deep brain stimulation in primary dystonia.
Schwingenschuh, P., Saifee, T.A., Katschnig-Winter, P., Reilly, M.M., Lunn, M.P., Manji, H., ...Rothwell, J.C. (2013). Cerebellar learning distinguishes inflammatory neuropathy with and without tremor.. Neurology, 80 (20), 1867-1873. doi:10.1212/WNL.0b013e318292a2b8
Hoffland, B.S., Kassavetis, P., Bologna, M., Teo, J.T.H., Bhatia, K.P., Rothwell, J.C., ...Van De Warrenburg, B.P. (2013). Cerebellum-dependent associative learning deficits in primary dystonia are normalized by rTMS and practice. European Journal of Neuroscience, 38 (1), 2166-2171. doi:10.1111/ejn.12186
Hoffland, B.S., Kassavetis, P., Bologna, M., Teo, J.T.H., Bhatia, K.P., Rothwell, J.C., ...van de Warrenburg, B.P. (2013). Cerebellum-dependent associative learning deficits in primary dystonia are normalized by rTMS and practice.. EUROPEAN JOURNAL OF NEUROSCIENCE, 38 (1), 2166-2171. doi:10.1111/ejn.12186
Pizza, F., Franceschini, C., Peltola, H., Vandi, S., Finotti, E., Ingravallo, F., ...Edwards, M.J. (2013). Clinical and polysomnographic course of childhood narcolepsy with cataplexy. Brain, 136 (12), 3787-3795. doi:10.1093/brain/awt277
Erro, R., Bhatia, K.P., Edwards, M.J., Farmer, S.F., Cordivari, C. (2013). Clinical diagnosis of propriospinal myoclonus is unreliable: An electrophysiologic study. Movement Disorders, 28 (13), 1868-1873. doi:10.1002/mds.25627
Erro, R., Bhatia, K.P., Edwards, M.J., Farmer, S.F., Cordivari, C. (2013). Clinical diagnosis of propriospinal myoclonus is unreliable: an electrophysiologic study.. MOVEMENT DISORDERS, 28 (13), 1868-1873. doi:10.1002/mds.25627
Mehta, A.R., Rowe, J.B., Trimble, M.R., Edwards, M.J., Bhatia, K.P., Schrag, A.E. (2013). Coactivation sign in fixed dystonia. PARKINSONISM & RELATED DISORDERS, 19 (4), 474-476. doi:10.1016/j.parkreldis.2012.10.014
Mehta, A.R., Rowe, J.B., Trimble, M.R., Edwards, M.J., Bhatia, K.P., Schrag, A.E. (2013). Coactivation sign in fixed dystonia. Parkinsonism and Related Disorders, 19 (4), 474-476. doi:10.1016/j.parkreldis.2012.10.014
Bhatia, K.P. (2013). Commentary for "Progressive ataxia associated with scarring skin lesions and vertical gaze palsy".. MOVEMENT DISORDERS, 28 (4), 445-446. doi:10.1002/mds.25466
Armstrong, M.J., Litvan, I., Lang, A.E., Bak, T.H., Bhatia, K.P., Borroni, B., ...Hallett, M. (2013). Criteria for the diagnosis of corticobasal degeneration.. NEUROLOGY, 80 (5), 496-503. doi:10.1212/WNL.0b013e31827f0fd1
Kefalopoulou, Z., Zrinzo, L., Aviles-Olmos, I., Bhatia, K., Jarman, P., Jahanshahi, M., ...Foltynie, T. (2013). Deep brain stimulation as a treatment for chorea-acanthocytosis. JOURNAL OF NEUROLOGY, 260 (1), 303-305. doi:10.1007/s00415-012-6714-0
Carecchio, M., Magliozzi, M., Copetti, M., Ferraris, A., Bernardini, L., Bonetti, M., ...Pellegrini, F. (2013). Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria.. MOVEMENT DISORDERS, 28 (6), 787-794. doi:10.1002/mds.25506
Erro, R., Bhatia, K.P., Edwards, M.J., Farmer, S.F., Cordivari, C. (2013). Does idiopathic propriospinal myoclonus exist ?.
Erro, R., Quinn, N.P., Schneider, S.A., Bhatia, K.P. (2013). Does rest tremor exclude the diagnosis of adult-onset primary dystonia?. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84 (6), 708. doi:10.1136/jnnp-2012-304779
McNeill, A., Wu, R.M., Tzen, K.Y., Aguiar, P.C., Arbelo, J.M., Barone, P., ...Bostantjopoulou, S. (2013). Dopaminergic Neuronal Imaging in Genetic Parkinson's Disease: Insights into Pathogenesis. PLOS ONE, 8 (7), doi:10.1371/journal.pone.0069190
Stamelou, M., Lai, S.C., Aggarwal, A., Schneider, S.A., Houlden, H., Yeh, T.-.H., ...Bhatia, K.P. (2013). Dystonic opisthotonus: a "red flag" for neurodegeneration with brain iron accumulation syndromes?. MOVEMENT DISORDERS, 28 (10), 1325-1329. doi:10.1002/mds.25490
Stamelou, M., Schneider, S.A., Batla, A., Bhatia, K.P., Lai, S.C., Yeh, T.-.H., ...Houlden, H. (2013). Dystonic opisthotonus: A "red flag" for neurodegeneration with brain iron accumulation syndromes?. Movement Disorders, 28 (10), 1325-1329. doi:10.1002/mds.25490
Schneider, S.A., Bhatia, K.P. (2013). EDITORIAL: METAL-RELATED NEUROLOGICAL DISORDERS: SEVERAL NEW GENES AND BETTER UNDERSTANDING PREFACE. METAL RELATED NEURODEGENERATIVE DISEASE, 110 XV-XVIII.
Burke, D.G., Rahim, A.A., Waddington, S.N., Karlsson, S., Enquist, I., Bhatia, K., ...Heales, S. (2013). Erratum to: Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes.. JOURNAL OF INHERITED METABOLIC DISEASE, 36 (6), 1089. doi:10.1007/s10545-013-9599-x
Moghadam, K.K., Pizza, F., Franceschini, C., Peltola, H., Vandi, S., Finotti, E., ...Dauvilliers, Y. (2013). Evolution of the clinical and polysomnographic picture of childhood narcolepsy with cataplexy following disease onset. JOURNAL OF NEUROLOGY, 260 S85-S86.
Schneider, S.A., Bhatia, K.P. (2013). Excess iron harms the brain: the syndromes of neurodegeneration with brain iron accumulation (NBIA).
Martino, D., Gajos, A., Gallo, V., Cif, L., Coubes, P., Tinazzi, M., ...Nardocci, N. (2013). Extragenetic factors and clinical penetrance of DYT1 dystonia: an exploratory study. JOURNAL OF NEUROLOGY, 260 (4), 1081-1086. doi:10.1007/s00415-012-6765-2
Pareés, I., Kassavetis, P., Saifee, T.A., Sadnicka, A., Davare, M., Bhatia, K.P., ...Edwards, M.J. (2013). Failure of explicit movement control in patients with functional motor symptoms. Movement Disorders, 28 (4), 517-523. doi:10.1002/mds.25287
Pareés, I., Kassavetis, P., Saifee, T.A., Sadnicka, A., Davare, M., Bhatia, K.P., ...Edwards, M.J. (2013). Failure of explicit movement control in patients with functional motor symptoms.. MOVEMENT DISORDERS, 28 (4), 517-523. doi:10.1002/mds.25287
Stamelou, M., Cossu, G., Edwards, M., Murgia, D., Parees, I., Melis, M., Bhatia, K.P. (2013). Familial functional movement disorders.
Stamelou, M., Cossu, G., Edwards, M.J., Murgia, D., Pareés, I., Melis, M., Bhatia, K.P. (2013). Familial psychogenic movement disorders.. MOVEMENT DISORDERS, 28 (9), 1295-1297. doi:10.1002/mds.25463
Pareés, I., Saifee, T.A., Kojovic, M., Kassavetis, P., Rubio-Agusti, I., Sadnicka, A., ...Edwards, M.J. (2013). Functional (psychogenic) symptoms in Parkinson's disease. Movement Disorders, 28 (12), 1622-1627. doi:10.1002/mds.25544
Pareés, I., Saifee, T.A., Kojovic, M., Kassavetis, P., Rubio-Agusti, I., Sadnicka, A., ...Edwards, M.J. (2013). Functional (psychogenic) symptoms in Parkinson's disease. MOVEMENT DISORDERS, 28 (12), 1622-1627. doi:10.1002/mds.25544
Batla, A., Stamelou, M., Edwards, M.J., Pareés, I., Saifee, T.A., Fox, Z., Bhatia, K.P. (2013). Functional movement disorders are not uncommon in the elderly.. MOVEMENT DISORDERS, 28 (4), 540-543. doi:10.1002/mds.25350
Macerollo, A., Bhatia, K.P. (2013). FUS gene mutations cause essential tremor: a surprise but also confirms genetic heterogeneity of essential tremor.. MOVEMENT DISORDERS, 28 (3), 290. doi:10.1002/mds.25376
Schneider, S.A., Dusek, P., Hardy, J., Westenberger, A., Jankovic, J., Bhatia, K.P. (2013). Genetics and Pathophysiology of Neurodegeneration with Brain Iron Accumulation (NBIA). CURRENT NEUROPHARMACOLOGY, 11 (1), 59-79.
Sadnicka, A., Teo, J., Kojovic, M., Kassavetis, P., Saifee, T., Isabel, P., ...Edwards, M. (2013). Genotype specific cerebellar involvement in dyt1 and dyt6 dystonia?. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84 (11), doi:10.1136/jnnp-2013-306573.159
Burke, D.G., Rahim, A.A., Waddington, S.N., Karlsson, S., Enquist, I., Bhatia, K., ...Heales, S. (2013). Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes.. JOURNAL OF INHERITED METABOLIC DISEASE, 36 (5), 869-872. doi:10.1007/s10545-012-9561-3
Mencacci, N., Polke, J., Stamelou, M., Sidle, K., Batla, A., Sweeney, M., ...Bhatia, K. (2013). Is GCH1 a risk locus for Parkinson's disease? Evidence from a case report. MOVEMENT DISORDERS, 28 S406.
Stamelou, M., Edwards, M.J., Bhatia, K.P. (2013). Late onset rest-tremor in DYT1 dystonia.. PARKINSONISM & RELATED DISORDERS, 19 (1), 136-137. doi:10.1016/j.parkreldis.2012.05.026
Batla, A., Panicker, J., Edwards, M., Stamelou, M., Parees, I., Kasavetis, P., Bhatia, K. (2013). LOWER URINARY TRACT SYMPTOMS IN FUNCTIONAL MOVEMENT DISORDERS.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84 (11), doi:10.1136/jnnp-2013-306573.149
Batla, A., Stamelou, M., Mensikova, K., Kaiserova, M., Tuckova, L., Kanovsky, P., ...Bhatia, K.P. (2013). Markedly asymmetric presentation in multiple system atrophy. Parkinsonism and Related Disorders, 19 (10), 901-905. doi:10.1016/j.parkreldis.2013.05.004
Batla, A., Stamelou, M., Mensikova, K., Kaiserova, M., Tuckova, L., Kanovsky, P., ...Bhatia, K.P. (2013). Markedly asymmetric presentation in multiple system atrophy.. PARKINSONISM & RELATED DISORDERS, 19 (10), 901-905. doi:10.1016/j.parkreldis.2013.05.004
Bhatia, K.P., Schneider, S.A. (2013). Metal Related Neurodegenerative Disease. Academic Press.
Sheerin, U.M., Stamelou, M., Charlesworth, G., Shiner, T., Spacey, S., Valente, E.M., ...Bhatia, K.P. (2013). Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation. Journal of Neurology, 260 (2), 656-660. doi:10.1007/s00415-012-6747-4
Sheerin, U.-.M., Stamelou, M., Charlesworth, G., Shiner, T., Spacey, S., Valente, E.-.M., ...Bhatia, K.P. (2013). Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation.. JOURNAL OF NEUROLOGY, 260 (2), 656-660. doi:10.1007/s00415-012-6747-4
Rubio-Agusti, I., Carecchio, M., Bhatia, K.P., Kojovic, M., Parees, I., Chandrashekar, H.S., ...Lachmann, R.H.L. (2013). Movement disorders in adult patients with classical galactosemia.. MOVEMENT DISORDERS, 28 (6), 804-810. doi:10.1002/mds.25348
Hersheson, J., Mencacci, N.E., Davis, M., MacDonald, N., Trabzuni, D., Ryten, M., ...Fawcett, K. (2013). Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia.. ANNALS OF NEUROLOGY, 73 (4), 546-553. doi:10.1002/ana.23832
Rosenzweig, I., Bhatia, K.P., Malhotra, T., Vukadinovic, Z., Scoffings, D.J. (2013). Neuropsychiatric Symptoms as a Putative Crescendo Warning of a Striatocapsular Infarct?. JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 25 (1), E39-E43. doi:10.1176/appi.neuropsych.12020039
Bhatia, K. (2013). Newly recognised atypical parkinsonian conditions-beyond MSA, PSP, CBD. JOURNAL OF NEUROLOGY, 260 S7.
Batla, A., Bhatia, K.P., Fisher, L., Joyce, E.M., Price, G., Edwards, M.J. (2013). Outcome after inpatient rehabilitation for patients with functional movement disorders.
Sadnicka, A., Pisarek, C., Ruge, D., Galea, J., Kassavetis, P., Pareés, I., ...Bhatia, K.P. (2013). Pallidal stimulation for cervical dystonia does not correct abnormal temporal discrimination. MOVEMENT DISORDERS, 28 (13), 1874-1877. doi:10.1002/mds.25581
Sadnicka, A., Kimmich, O., Pisarek, C., Ruge, D., Galea, J., Kassavetis, P., ...Bradley, D. (2013). Pallidal stimulation for cervical dystonia does not correct abnormal temporal discrimination. Movement Disorders, 28 (13), 1874-1877. doi:10.1002/mds.25581
Aguirregomozcorta, M., Stamelou, M., Antonini, A., Schwingenschuh, P., Prvulovich, L., Edwards, M.J., ...Bhatia, K.P. (2013). Patients with rest-tremor and scans with ipsilateral dopaminergic deficit.. JOURNAL OF NEUROLOGY, 260 (4), 1132-1135. doi:10.1007/s00415-012-6774-1
Batla, A., Stamelou, M., Bhatia, K.P. (2013). Patients with scans without evidence of dopaminergic deficit (SWEDD) do not have Parkinson's disease- A long term follow up study.
Albanese, A., Bhatia, K., Bressman, S.B., DeLong, M.R., Fahn, S., Fung, V.S.C., ...Klein, C. (2013). Phenomenology and classification of dystonia: A consensus update. MOVEMENT DISORDERS, 28 (7), 863-873. doi:10.1002/mds.25475
Charlesworth, G., Bhatia, K.P. (2013). Primary and secondary dystonic syndromes: an update.. Curr Opin Neurol, 26 (4), 406-412. doi:10.1097/WCO.0b013e3283633696
Stamelou, M., Pisani, A., Edwards, M., Bhatia, K.P. (2013). Primary lateral sclerosis with marked supranuclear gaze palsy and postural instability but normal dopamine transporters imaging: A distinct PLS phenotype.
Stamelou, M., Adams, M., Davagnanam, I., Batla, A., Sheerin, U., Talbot, K., Bhatia, K.P. (2013). Progressive ataxia and palatal tremor associated with dense pontine calcification: A unique case.. Mov Disord, 28 (8), 1155-1157. doi:10.1002/mds.25310
Balint, B., Bhatia, K. (2013). Reopening the case for anti-basal ganglia antibodies (ABGAs): Identification of dopamine-2 receptor antibodies associated with movement disorders. MOVEMENT DISORDERS, 28 (6), 733. doi:10.1002/mds.25454
Edwards, M.J., Lang, A.E., Bhatia, K.P. (2013). Reply to Drs. Kurlan, Fasano, and Evans: A clinically useful definition of stereotypies.. MOVEMENT DISORDERS, 28 (3), 405-406. doi:10.1002/mds.25253
Erro, R., Rubio-Agusti, I., Saifee, T.A., Cordivari, C., Ganos, C., Batla, A., Bhatia, K.P. (2013). Rest and other types of tremor in adult-onset primary dystonia.. Journal of Neurology, Neurosurgery & Psychiatry, doi:10.1136/jnnp-2013-305876
Batla, A., Stamelou, M., Mencacci, N., Schapira, A.H., Bhatia, K.P. (2013). Ropinirole monotherapy induced severe reversible dyskinesias in Parkinson's disease.. Mov Disord, 28 (8), 1159-1160. doi:10.1002/mds.25318
Kojovic, M., Pareés, I., Kassavetis, P., Palomar, F.J., Mir, P., Teo, J.T., ...Edwards, M.J. (2013). Secondary and primary dystonia: pathophysiological differences.. BRAIN, 136 2038-2049. doi:10.1093/brain/awt150
Kägi, G., Katschnig, P., Fiorio, M., Tinazzi, M., Ruge, D., Rothwell, J., Bhatia, K.P. (2013). Sensory tricks in primary cervical dystonia depend on visuotactile temporal discrimination.. MOVEMENT DISORDERS, 28 (3), 356-361. doi:10.1002/mds.25305
Pichler, I., Del Greco, M.F., Gogele, M., Lill, C.M., Bertram, L., Do, C.B., ...Nalls, M. (2013). Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study. PLoS.Med., 10 (6), e1001462-. doi:10.1371/journal.pmed.1001462
Miquel, M., Spampinato, U., Latxague, C., Aviles-Olmos, I., Bader, B., Bertram, K., ...Cho, J.W. (2013). Short and long term outcome of bilateral pallidal stimulation in chorea-acanthocytosis.. PLoS One, 8 (11), doi:10.1371/journal.pone.0079241
Kara, E., Schottlaender, L., Berardo, A., Reisin, R., Hehir, J., Hughes, D., ...Preza, E. (2013). SPG11 sequencing in worldwide populations of familial and sporadic spastic paraplegia patients reveals frequent mutations and the common association of parkinsonian features. MOVEMENT DISORDERS, 28 S397.
Batla, A., Stamelou, M., Bhatia, K.P. (2013). Syringomyelia with cervical dystonia - A report of two cases.
Martino, D., Stamelou, M., Bhatia, K.P. (2013). The differential diagnosis of Huntington's disease-like syndromes: 'red flags' for the clinician. Journal of Neurology, Neurosurgery and Psychiatry, 84 (6), 650-656. doi:10.1136/jnnp-2012-302532
Bhatia, K.P., Sheerin, U., Stamelou, M. (2013). The entity of parkinsonism and associated lipomatosis.
van der Salm, S.M.A., de Haan, R.J., Cath, D.C., van Rootselaar, A.-.F., Tijssen, M.A.J. (2013). The eye of the beholder: inter-rater agreement among experts on psychogenic jerky movement disorders. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84 (7), 742-747. doi:10.1136/jnnp-2012-304113
Schrag, A.E., Mehta, A.R., Bhatia, K.P., Brown, R.J., Frackowiak, R.S., Trimble, M.R., ...Rowe, J.B. (2013). The functional neuroimaging correlates of psychogenic versus organic dystonia. Brain, 136 770-781. doi:10.1093/brain/awt008
Charlesworth, G., Bhatia, K.P., Wood, N.W. (2013). The genetics of dystonia: new twists in an old tale.. Brain, 136 (7), 2017-2037. doi:10.1093/brain/awt138
Duran, R., Mencacci, N.E., Angeli, A.V., Shoai, M., Deas, E., Houlden, H., ...Deegan, P. (2013). The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease. Movement Disorders, 28 (2), 232-236. doi:10.1002/mds.25248
Kojovic, M., Pareés, I., Lampreia, T., Pienczk-Reclawowicz, K., Xiromerisiou, G., Rubio-Agusti, I., ...Brancati, F. (2013). The syndrome of deafness-dystonia: clinical and genetic heterogeneity.. MOVEMENT DISORDERS, 28 (6), 795-803. doi:10.1002/mds.25394
Klebe, S., Golmard, J.L., Nalls, M.A., Saad, M., Singleton, A.B., Bras, J.M., ...Kuhlenbäumer, G. (2013). The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. Journal of Neurology, Neurosurgery and Psychiatry, 84 (6), 666-673. doi:10.1136/jnnp-2012-304475
Saifee, T.A., Schwingenschuh, P., Reilly, M.M., Lunn, M.P.T., Katschnig, P., Kassavetis, P., ...Rothwell, J.C. (2013). Tremor in inflammatory neuropathies. Journal of Neurology, Neurosurgery and Psychiatry, 84 (11), 1282-1287. doi:10.1136/jnnp-2012-303013
Saifee, T.A., Schwingenschuh, P., Reilly, M.M., Lunn, M.P.T., Katschnig, P., Kassavetis, P., ...Rothwell, J.C. (2013). Tremor in inflammatory neuropathies.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84 (11), 1282-1287. doi:10.1136/jnnp-2012-303013
Rubio-Agusti, I., Pareés, I., Kojovic, M., Stamelou, M., Saifee, T.A., Charlesworth, G., ...Bhatia, K.P. (2013). Tremulous cervical dystonia is likely to be familial: Clinical characteristics of a large cohort. Parkinsonism and Related Disorders, 19 (6), 634-638. doi:10.1016/j.parkreldis.2013.02.017
Rubio-Agusti, I., Pareés, I., Kojovic, M., Stamelou, M., Saifee, T.A., Charlesworth, G., ...Bhatia, K.P. (2013). Tremulous cervical dystonia is likely to be familial: clinical characteristics of a large cohort.. PARKINSONISM & RELATED DISORDERS, 19 (6), 634-638. doi:10.1016/j.parkreldis.2013.02.017
Erro, R., Bhatia, K.P., Catania, S., Shields, K., Cordivari, C. (2013). When the levator scapulae becomes a "rotator capitis": implications for cervical dystonia.. PARKINSONISM & RELATED DISORDERS, 19 (7), 705-706. doi:10.1016/j.parkreldis.2013.03.012
Hayflick, S.J., Kruer, M.C., Gregory, A., Haack, T.B., Kurian, M.A., Houlden, H.H., ...Harik, S.I. (2013). β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation.. BRAIN, 136 1708-1717. doi:10.1093/brain/awt095

2012

Stamelou, M., Bhatia, K.P. (2012). A new treatable genetic disorder of manganese metabolism causing dystonia-parkinsonism and cirrhosis: the "new" Wilson's disease?. Movement Disorders, 27 (8), 962. doi:10.1002/mds.25031
Kruer, M.C., Paudel, R., Wagoner, W., Sanford, L., Kara, E., Gregory, A., ...Hardy, J. (2012). Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts. Neuroscience Letters, 523 (1), 35-38. doi:10.1016/j.neulet.2012.06.036
Kruer, M.C., Paudel, R., Wagoner, W., Sanford, L., Kara, E., Gregory, A., ...Hardy, J. (2012). Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts.. NEUROSCIENCE LETTERS, 523 (1), 35-38. doi:10.1016/j.neulet.2012.06.036
Rubio-Agusti, I., Kojovic, M., Edwards, M.J., Murphy, E., Chandrashekar, H.S., Lachmann, R.H., Bhatia, K.P. (2012). Atypical Parkinsonism and Cerebrotendinous Xanthomatosis: Report of a Family With Corticobasal Syndrome and a Literature Review. MOVEMENT DISORDERS, 27 (14), 1769-1774. doi:10.1002/mds.25229
Rubio-Agusti, I., Kojovic, M., Edwards, M.J., Chandrasehkar, H.S., Bhatia, K.P., Murphy, E., Lachmann, R.H. (2012). ATYPICAL PARKINSONISM AND CEREBROTENDINOUS XANTHOMATOSIS: REPORT OF A FAMILY WITH CORTICOBASAL SYNDROME AND LITERATURE REVIEW. JOURNAL OF INHERITED METABOLIC DISEASE, 35 S24.
Agusti, I.R., Kojovic, M., Edwards, M.J., Murphy, E., Lachmann, R., Bhatia, K.P. (2012). Atypical parkinsonism in Cerebrotendinous Xanthomatosis (CTX): A family with corticobasal syndrome (CBS).
Pareés, I., Saifee, T.A., Kassavetis, P., Kojovic, M., Rubio-Agusti, I., Rothwell, J.C., ...Edwards, M.J. (2012). Believing is perceiving: mismatch between self-report and actigraphy in psychogenic tremor.. BRAIN, 135 117-123. doi:10.1093/brain/awr292
Bhatia, K. (2012). Beware of YouTube: movement disorders on internet.
Doherty, K.M., Silveira-Moriyama, L., Giladi, N., Bhatia, K.P., Parton, M., Lees, A.J. (2012). Camptocormia: Don't forget muscle disease in the movement disorder clinic. Journal of Neurology, 259 (8), 1752-1754. doi:10.1007/s00415-012-6448-z
Doherty, K.M., Silveira-Moriyama, L., Giladi, N., Bhatia, K.P., Parton, M., Lees, A.J. (2012). Camptocormia: don't forget muscle disease in the movement disorder clinic.. JOURNAL OF NEUROLOGY, 259 (8), 1752-1754. doi:10.1007/s00415-012-6448-z
Rubio-Agusti, I., Kojovic, M., Chandrashekar, H.S., Edwards, M.J., Bhatia, K.P. (2012). Cervical dystonia and joint hypermobility syndrome: a dangerous combination.. MOVEMENT DISORDERS, 27 (2), 203-204. doi:10.1002/mds.24013
Massano, J., Bhatia, K.P. (2012). Clinical approach to Parkinson's disease: features, diagnosis, and principles of management.. COLD SPRING HARBOR PERSPECTIVES IN MEDICINE, 2 (6), doi:10.1101/cshperspect.a008870
Bhatia, K.P., Massano, J. (2012). Clinical approach to Parkinson's disease:features, diagnosis, and principles of management. In Parkinson's Disease. .
Kara, E., Xiromerisiou, G., Paudel, R., Revesz, T., Holton, J., Lees, A., ...Foltynie, T. (2012). Comprehensive genetic investigation of NBIA and complex dystonia-parkinsonism.
Kassavetis, P., Saifee, T.A., Roussos, G., Drougkas, L., Kojovic, M., Rothwell, J.C., ...Bhatia, K.P. (2012). Developing a tool for remote digital assessment of Parkinson's disease.
Saifee, T.A., Kassavetis, P., Drougkas, L., Roussos, G., Parees, I., Schwingenschuh, P., ...Edwards, M.J. (2012). Diagnosis of psychogenic tremor using a smartphone.
Shiner, T., Seymour, B., Wunderlich, K., Hill, C., Bhatia, K.P., Dayan, P., Dolan, R.J. (2012). Dopamine and performance in a reinforcement learning task: evidence from Parkinson's disease.. Brain, 135 (6), 1871-1883. doi:10.1093/brain/aws083
Stamelou, M., Alonso-Canovas, A., Bhatia, K. (2012). Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases.
Stamelou, M., Alonso-Canovas, A., Bhatia, K.P. (2012). Dystonia in corticobasal degeneration: a review of the literature on 404 pathologically proven cases.. MOVEMENT DISORDERS, 27 (6), 696-702. doi:10.1002/mds.24992
Stamelou, M., Tuschl, K., Chong, W.K., Burroughs, A.K., Mills, P.B., Bhatia, K.P., Clayton, P.T. (2012). Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: A new treatable disorder. MOVEMENT DISORDERS, 27 (10), 1317-1322. doi:10.1002/mds.25138
Stamelou, M., Tuschl, K., Mills, P., Chong, K., Burroughs, A., Clayton, P., Bhatia, K. (2012). Early-onset dystonia with brain manganese accumulation due to SLC30A10 mutations: a new treatable disorder.
Saifee, T.A., Kassavetis, P., Parees, I., Lampreia, T., Murase, N., Hoffland, B., ...Edwards, M.J. (2012). Enhancement of the pre-movement potential of a psychogenic movement using a sequential movement paradigm.
Charlesworth, G., Bras, J.M., Guerreiro, R., Sheerin, U.M., Bhatia, K., Wood, N.W. (2012). Exome Sequencing Identifies Two Separate Mutations in a Novel Gene as Cause of Autosomal Dominant Cervical Dystonia in Two Families.
Haack, T.B., Hogarth, P., Kruer, M.C., Gregory, A., Wieland, T., Schwarzmayr, T., ...Kara, E. (2012). Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA. American Journal of Human Genetics, 91 (6), 1144-1149. doi:10.1016/j.ajhg.2012.10.019
Haack, T.B., Hogarth, P., Kruer, M.C., Gregory, A., Wieland, T., Schwarzmayr, T., ...Kara, E. (2012). Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (6), 1144-1149. doi:10.1016/j.ajhg.2012.10.019
Edwards, M.J., Bhatia, K.P. (2012). Functional (psychogenic) movement disorders: merging mind and brain.. LANCET NEUROLOGY, 11 (3), 250-260. doi:10.1016/S1474-4422(11)70310-6
Schrag, A.E., Mehta, A.R., Bhatia, K.P., Brown, R.J., Frackowiak, R.S.J., Trimble, M.R., ...Rowe, J.B. (2012). Functional neuroimaging of psychogenic dystonia.
Kojovic, M., Kassavetis, P., Bologna, M., Berardelli, A., Rothwell, J., Edwards, M., Bhatia, K. (2012). Functional Reorganisation in Sensorimotor Cortex Is a Compensatory Mechanism in Early Parkinson's Disease: A Six Months Follow-Up Study.
Kojovic, M., Bologna, M., Kassavetis, P., Murase, N., Palomar, F.J., Berardelli, A., ...Bhatia, K.P. (2012). Functional reorganization of sensorimotor cortex in early Parkinson disease.. NEUROLOGY, 78 (18), 1441-1448. doi:10.1212/WNL.0b013e318253d5dd
Mok, K.Y., Kasperaviciute, D., Schneider, S.A., Pickering-Brown, S.M., Silverdale, M., Edwards, M.J., ...Hardy, J. (2012). Genome wide association study in cervical dystonia.
Bhatia, K.P., Schneider, S.A. (2012). Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesia.. MOVEMENT DISORDERS, 27 (6), 707. doi:10.1002/mds.25038
Batla, A., Kassavetis, P., Parees, I., Bhatia, K., Edwards, M.J. (2012). Impaired initiation of voluntary contraction on a reaction time task may support the clinical diagnosis in fixed dystonia.
Sadnicka, A., Kimmich, O., Pisarek, C., Galea, J., Kassavetis, P., Saifee, T.A., ...Hariz, M. (2012). Internal globus pallidus stimulation and temporal discrimination thresholds in cervical dystonia - Preliminary data suggests that clinical improvement does not represent improved sensory function.
Pilurzi, G., Saifee, T.A., Bhatia, K.P., Edwards, M.J., Deriu, F., Rothwell, J.C. (2012). Intracortical and brainstem excitability in patients with oro-mandibular dystonia.
Mencacci, N.E., Labrum, R., Haworth, A., Sweeney, M., Pittman, A., Stamelou, M., ...Houlden, H. (2012). Is anything lying behind parkin heterozygous mutations?.
Sadnicka, A., Hamada, M., Kojovic, M., Kassavetis, P., Parees, I., Saifee, T.A., ...Edwards, M.J. (2012). Is synaptic plasticity normal in writer's cramp? Anodal cerebellar stimulation shows promising preliminary evidence that it can modulate PAS in dystonia.
Stockner, H., Schwingenschuh, P., Djamshidian, A., Silveira-Moriyama, L., Katschnig, P., Seppi, K., ...Poewe, W. (2012). Is transcranial sonography useful to distinguish scans without evidence of dopaminergic deficit patients from Parkinson's disease?. Movement Disorders, 27 (9), 1182-1185. doi:10.1002/mds.25102
Stockner, H., Schwingenschuh, P., Djamshidian, A., Silveira-Moriyama, L., Katschnig, P., Seppi, K., ...Poewe, W. (2012). Is transcranial sonography useful to distinguish scans without evidence of dopaminergic deficit patients from Parkinson's disease?. Movement Disorders, 27 (9), 1182-1185. doi:10.1002/mds.25102
Stamelou, M., Saifee, T., Edwards, M., Bhatia, K. (2012). Isolated palatal tremor: Reappraisal suggests psychogenic aetiology in majority of one case series.
Kassavetis, P., Batla, A., Pareés, I., Saifee, T.A., Schrag, A., Cordivari, C., ...Edwards, M.J. (2012). Joint hypermobility syndrome: A risk factor for fixed dystonia?. Movement Disorders, 27 (8), 1070. doi:10.1002/mds.25004
Kassavetis, P., Batla, A., Pareés, I., Saifee, T.A., Schrag, A., Cordivari, C., ...Edwards, M.J. (2012). Joint hypermobility syndrome: a risk factor for fixed dystonia?. MOVEMENT DISORDERS, 27 (8), 1070. doi:10.1002/mds.25004
Pareés, I., Kassavetis, P., Saifee, T.A., Sadnicka, A., Bhatia, K.P., Fotopoulou, A., Edwards, M.J. (2012). 'Jumping to conclusions' bias in functional movement disorders.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 83 (4), 460-463. doi:10.1136/jnnp-2011-300982
Stamelou, M., Edwards, M., Bhatia, K. (2012). Late onset rest-tremor in DYT1 dystonia.
Donaldson, I., Marsden, C.D., Schneider, S., Bhatia, K. (2012). Marsden's Book of Movement Disorders. Oxford University Press, USA.
Katschnig, P., Schwingenschuh, P., Davare, M., Sadnicka, A., Schmidt, R., Rothwell, J.C., ...Edwards, M.J. (2012). Motor learning in primary cervical dystonia.
Katschnig, P., Schwingenschuh, P., Davare, M., Sadnicka, A., Schmidt, R., Rothwell, J.C., ...Edwards, M.J. (2012). Motor sequence learning and motor adaptation in primary cervical dystonia.
Stamelou, M., Edwards, M., Espay, A., Fung, V., Hallett, M., Lang, A., ...Bhatia, K. (2012). Movement disorders on YouTube: Caveat spectator.
Batla, A., Stamelou, M., Bhatia, K.P. (2012). Multiple system atrophy presenting like corticobasal syndrome at onset.
Charlesworth, G., Plagnol, V., Holmström, K.M., Bras, J., Sheerin, U.-.M., Preza, E., ...Stamelou, M. (2012). Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.. The American Journal of Human Genetics, 91 (6), 1041-1050. doi:10.1016/j.ajhg.2012.10.024
Lee, H.-.Y., Huang, Y., Bruneau, N., Roll, P., Roberson, E.D.O., Hermann, M., ...Ashizawa, T. (2012). Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions. CELL REPORTS, 1 (1), 2-12. doi:10.1016/j.celrep.2011.11.001
Lee, H.-.Y., Huang, Y., Bruneau, N., Roll, P., Roberson, E.D.O., Hermann, M., ...Ashizawa, T. (2012). Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions. NEUROLOGY, 78
Lee, H.-.Y., Huang, Y., Bruneau, N., Roll, P., Roberson, E.D.O., Hermann, M., ...Ashizawa, T. (2012). Mutations in the Novel Protein PRRT2 Cause Infantile Convulsions with Paroxysmal Kinesigenic Dyskinesia.
Lee, H.-.Y., Huang, Y., Edwards, R., Hanna, M., Bowcock, A., Szepetowski, P., ...Ptacek, L. (2012). Mutations in the Novel Protein PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions.
Stamelou, M., Mencacci, N., Cordivari, C., Batla, A., Houlden, H., Wood, N., ...Bhatia, K. (2012). Myoclonic dystonia syndrome due to tyrosine hydroxylase deficiency.
Stamelou, M., Mencacci, N.E., Cordivari, C., Batla, A., Wood, N.W., Houlden, H., ...Bhatia, K.P. (2012). Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency.. NEUROLOGY, 79 (5), 435-441. doi:10.1212/WNL.0b013e318261714a
Kruer, M.C., Boddaert, N., Schneider, S.A., Houlden, H., Bhatia, K.P., Gregory, A., ...Hayflick, S.J. (2012). Neuroimaging features of neurodegeneration with brain iron accumulation.. AMERICAN JOURNAL OF NEURORADIOLOGY, 33 (3), 407-414. doi:10.3174/ajnr.A2677
Burke, A., Mantuano, E., Bhatia, K.P., Veneziano, L., Giunti, P. (2012). NOVEL DE NOVO MUTATION CAUSING BENIGN HEREDITARY CHOREA WITH HYPOTHRYOIDISM AND A PITUITARY MASS.
Carrechio, M., Massano, J., Bhatia, K.P. (2012). Paroxysmal Dyskinesias. In Hyperkinetic Movement Disorders, with Desktop Edition Differential Diagnosis and Treatment. John Wiley & Sons.
Stamelou, M., Aguirregomozcorta, M., Antonini, A., Schwingenschuh, P., Prulovich, L., Dickson, J.C., ...Bhatia, K.P. (2012). Patients with rest-tremor and scans with ipsilateral dopaminergic deficit: (SWIDD).
Parees, I., Kojovic, M., Pires, M., Agusti, I.R., Saifee, T.A., Sadnicka, A., ...Edwards, M.J. (2012). Physical precipitating factors in functional movement disorders.
Lampreia, T., Saifee, T.A., Chen, J.A., Parees, I., Kassavetis, P., Sadnicka, A., ...Edwards, M.J. (2012). Pre-movement potentials in tics: Are these associated with the urge to move?.
Stamelou, M., Batla, A., Bhatia, K. (2012). Progressive ataxia and palatal tremor due to isolated pontine calcification: a novel case.
Gardiner, A.R., Bhatia, K.P., Stamelou, M., Dale, R.C., Kurian, M.A., Schneider, S.A., ...Spacey, S.D. (2012). PRRT2 gene mutations From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. NEUROLOGY, 79 (21), 2115-2121. doi:10.1212/WNL.0b013e3182752c5a
Sheerin, U.M., Stamelou, M., Charlesworth, G., Shiner, T., Spacey, S., Valente, E.M., ...Bhatia, K. (2012). PRRT2 gene mutations in a large family with paroxysmal kinesigenic dyskinesia and co-segregation with migraine with aura.
Gardiner, A.R., Bhatia, K.P., Stamelou, M., Dale, R.C., Kurian, M.A., Schneider, S.A., ...Spacey, S.D. (2012). PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.. MOVEMENT DISORDERS, 27 S448.
Fasano, A., Valadas, A., Bhatia, K.P., Prashanth, L.K., Lang, A.E., Munhoz, R.P., ...Girlanda, P. (2012). Psychogenic facial movement disorders: Clinical features and associated conditions. MOVEMENT DISORDERS, 27 (12), 1544-1551. doi:10.1002/mds.25190
Batla, A., Stamelou, M., Edwards, M.J., Parees, I., Saifee, T.A., Bhatia, K.P. (2012). Psychogenic movement disorders in older people - Clinical profile and associated features.
Stamelou, M., Saifee, T.A., Edwards, M.J., Bhatia, K.P. (2012). Psychogenic palatal tremor may be underrecognized: reappraisal of a large series of cases.. Mov Disord, 27 (9), 1164-1168. doi:10.1002/mds.24948
Depienne, C., Bouteiller, D., Meneret, A., Billot, S., Groppa, S., Klebe, S., ...Brueggemann, N. (2012). RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans. AMERICAN JOURNAL OF HUMAN GENETICS, 90 (2), 301-307. doi:10.1016/j.ajhg.2011.12.002
Sheerin, U.M., Charlesworth, G., Bras, J., Guerreiro, R., Bhatia, K., Foltynie, T., ...Wood, N. (2012). Screening for VPS35 mutations in Parkinson's disease. Neurobiology of Aging, 33 (4), 838.e1-838.e5. doi:10.1016/j.neurobiolaging.2011.10.032
Sheerin, U.-.M., Charlesworth, G., Bras, J., Guerreiro, R., Bhatia, K., Foltynie, T., ...Wood, N. (2012). Screening for VPS35 mutations in Parkinson's disease.. NEUROBIOLOGY OF AGING, 33 (4), doi:10.1016/j.neurobiolaging.2011.10.032
Kojovic, M., Edwards, M.J., Parees, I., Rothwell, J.C., Bhatia, K.P. (2012). Secondary cervical dystonia caused by cerebellar cystic lesion--a case study with transcranial magnetic stimulation.. CLINICAL NEUROPHYSIOLOGY, 123 (2), 418-419. doi:10.1016/j.clinph.2011.06.015
Edwards, M.J., Lang, A.E., Bhatia, K.P. (2012). Stereotypies: a critical appraisal and suggestion of a clinically useful definition.. MOVEMENT DISORDERS, 27 (2), 179-185. doi:10.1002/mds.23994
Schneider, S.A., Bhatia, K.P. (2012). Syndromes of Neurodegeneration With Brain Iron Accumulation. SEMINARS IN PEDIATRIC NEUROLOGY, 19 (2), 57-66. doi:10.1016/j.spen.2012.03.005
Schneider, S.A., Hardy, J., Bhatia, K.P. (2012). Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations.. MOVEMENT DISORDERS, 27 (1), 42-53. doi:10.1002/mds.23971
Teo, J.T., Edwards, M.J., Bhatia, K. (2012). Tardive dyskinesia is caused by maladaptive synaptic plasticity: a hypothesis.. MOVEMENT DISORDERS, 27 (10), 1205-1215. doi:10.1002/mds.25107
Xiromerisiou, G., Houlden, H., Scarmeas, N., Stamelou, M., Kara, E., Hardy, J., ...Paudel, R. (2012). THAP1 mutations and dystonia phenotypes: A metanalysis, genotype phenotype correlations and identification of novel mutations.
Xiromerisiou, G., Houlden, H., Scarmeas, N., Stamelou, M., Kara, E., Hardy, J., ...Paudel, R. (2012). THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations. Movement Disorders, 27 (10), 1290-1294. doi:10.1002/mds.25146
Xiromerisiou, G., Houlden, H., Scarmeas, N., Stamelou, M., Kara, E., Hardy, J., ...Paudel, R. (2012). THAP1 mutations and dystonia phenotypes: genotype phenotype correlations.. MOVEMENT DISORDERS, 27 (10), 1290-1294. doi:10.1002/mds.25146
Kojovic, M., Pareés, I., Sadnicka, A., Kassavetis, P., Rubio-Agusti, I., Saifee, T.A., ...Bhatia, K.P. (2012). The brighter side of music in dystonia.. ARCHIVES OF NEUROLOGY, 69 (7), 917-919. doi:10.1001/archneurol.2012.33
Sadnicka, A., Hoffland, B.S., Bhatia, K.P., van de Warrenburg, B.P., Edwards, M.J. (2012). The cerebellum in dystonia - help or hindrance?. CLINICAL NEUROPHYSIOLOGY, 123 (1), 65-70. doi:10.1016/j.clinph.2011.04.027
Stamelou, M., Plazzi, G., Lugaresi, E., Edwards, M.J., Bhatia, K.P. (2012). The distinct movement disorder in anti-NMDA receptor encephalitis may be related to Status Dissociatus: a hypothesis.. MOVEMENT DISORDERS, 27 (11), 1360-1363. doi:10.1002/mds.25072
Shiner, T., Seymour, B., Symmonds, M., Dayan, P., Bhatia, K.P., Dolan, R.J. (2012). The effect of motivation on movement: a study of bradykinesia in Parkinson's disease.. PLOS One, 7 (10), doi:10.1371/journal.pone.0047138
Stamelou, M., Edwards, M.J., Hallett, M., Bhatia, K.P. (2012). The non-motor syndrome of primary dystonia: clinical and pathophysiological implications.. BRAIN, 135 1668-1681. doi:10.1093/brain/awr224
Polke, J., Mencacci, N., Stamelou, M., Sweeney, M.G., Manji, H., Wood, N.W., ...Houlden, H. (2012). Transcript analysis of a variably-penetrant GTP cyclohydrolase intronic splicing mutation.
Batla, A., Stamelou, M., Bhatia, K.P. (2012). Treatment of focal dystonia.. CURRENT TREATMENT OPTIONS IN NEUROLOGY, 14 (3), 213-229. doi:10.1007/s11940-012-0169-6
Batla, A., Bhatia, K.P., Parees, I., Kassavetis, P., Edwards, M.J., Stamelou, M., Panicker, J. (2012). Urinary dysfunction in patients with fixed dystonia - A prospective study.
Mittag, F., Buechel, F., Saad, M., Jahn, A., Schulte, C., Bochdanovits, Z., ...Hernandez, D.G. (2012). Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities. HUMAN MUTATION, 33 (12), 1708-1718. doi:10.1002/humu.22161
Keller, M.F., Saad, M., Bras, J., Bettella, F., Nicolaou, N., Simon-Sanchez, J., ...Gibbs, J.R. (2012). Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. HUMAN MOLECULAR GENETICS, 21 (22), 4996-5009. doi:10.1093/hmg/dds335
Kassavetis, P., Saifee, T.A., Sadnicka, A., Parees, I., Kojovic, M., Bhatia, K.P., ...Edwards, M.J. (2012). Using vibration training to increase the strength of surround inhibition in healthy controls and patients with hand dystonia.
Paisán-Ruiz, C., Li, A., Schneider, S.A., Holton, J.L., Johnson, R., Kidd, D., ...Hardy, J. (2012). Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations.. NEUROBIOLOGY OF AGING, 33 (4), 814-823. doi:10.1016/j.neurobiolaging.2010.05.009
Kojovic, M., Sheerin, U., Rubio-Agusti, I., Bras, J., Wood, N., Houlden, H., ...Bhatia, K. (2012). Young Onset Parkinson's Disease Due to Homozygous Duplication of SNCA in a Consanguineous Family from Pakistan.
Kojovic, M., Sheerin, U.-.M., Rubio-Agusti, I., Saha, A., Bras, J., Gibbons, V., ...Wood, N.W. (2012). Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.. Mov Disord, 27 (14), 1829-1830. doi:10.1002/mds.25199
Kojovic, M., Sheerin, U.M., Rubio-Agusti, I., Saha, A., Bras, J., Gibbons, V., ...Wood, N.W. (2012). Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.. Movement disorders : official journal of the Movement Disorder Society, 27 (14), 1827-1829. doi:10.1002/mds.25114

2011

Talelli, P., Hoffland, B.S., Schneider, S.A., Edwards, M.J., Bhatia, K.P., van de Warrenburg, B.P.C., Rothwell, J.C. (2011). A distinctive pattern of cortical excitability in patients with the syndrome of dystonia and cerebellar ataxia.. CLINICAL NEUROPHYSIOLOGY, 122 (9), 1816-1819. doi:10.1016/j.clinph.2011.02.029
Djarmati-Westenberger, A., Brueggemann, N., Espay, A.J., Bhatia, K.P., Klein, C. (2011). A NOVEL DCC MUTATION AND GENETIC HETEROGENEITY IN CONGENITAL MIRROR MOVEMENTS. NEUROLOGY, 77 (16), 1580. doi:10.1212/WNL.0b013e318230b140
Plagnol, V., Nalls, M.A., Bras, J.M., Hernandez, D.G., Sharma, M., Sheerin, U.-.M., ...Lesage, S. (2011). A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease. PLoS Genetics, 7 (6), doi:10.1371/journal.pgen.1002142
Stamelou, M., Kojovic, M., Edwards, M.J., Bhatia, K.P. (2011). Ability to cycle despite severe freezing of gait in atypical parkinsonism in Fahr's syndrome.. MOVEMENT DISORDERS, 26 (11), 2141-2142. doi:10.1002/mds.23794
Edwards, M.J., Moretto, G., Schwingenschuh, P., Katschnig, P., Bhatia, K.P., Haggard, P. (2011). Abnormal sense of intention preceding voluntary movement in patients with psychogenic tremor.. NEUROPSYCHOLOGIA, 49 (9), 2791-2793. doi:10.1016/j.neuropsychologia.2011.05.021
Bhatia, K., Frydenberg, E., Steel, T., Ow-Yang, M. (2011). An anterior expandable titanium cage in Mycobacterium avium vertebral osteomyelitis. Journal of Clinical Neuroscience, 18 (3), 431-434. doi:10.1016/j.jocn.2010.07.108
Van Poppelen, D., Saifee, T.A., Schwingenschuh, P., Katschnig, P., Bhatia, K.P., Tijssen, M.A., Edwards, M.J. (2011). Attention to self in psychogenic tremor.
van Poppelen, D., Saifee, T.A., Schwingenschuh, P., Katschnig, P., Bhatia, K.P., Tijssen, M.A., Edwards, M.J. (2011). Attention to self in psychogenic tremor.. MOVEMENT DISORDERS, 26 (14), 2575-2576. doi:10.1002/mds.23911
Kojovic, M., Caronni, A., Bologna, M., Rothwell, J.C., Bhatia, K.P., Edwards, M.J. (2011). Botulinum toxin injections reduce associative plasticity in patients with primary dystonia.. MOVEMENT DISORD, 26 (7), 1282-1289. doi:10.1002/mds.23681
Kassavetis, P., Hoffland, B.S., Saifee, T.A., Bhatia, K.P., van de Warrenburg, B.P., Rothwell, J.C., Edwards, M.J. (2011). Cerebellar brain inhibition is decreased in active and surround muscles at the onset of voluntary movement.. EXPERIMENTAL BRAIN RESEARCH, 209 (3), 437-442. doi:10.1007/s00221-011-2575-5
Pareés, I., Kojovic, M., Prasad Korlipara, L.V., Bhatia, K.P. (2011). Cervical dystonia associated with facioscapulohumeral dystrophy: expanding the clinical spectrum?. MOVEMENT DISORDERS, 26 (4), 765-766. doi:10.1002/mds.23516
Rubio-Agusti, I., Edwards, M., Bhatia, K. (2011). Cervical subluxation complicating cervical dystonia.
Stamelou, M., Rubio-Agusti, I., Quinn, N., Bhatia, K. (2011). Characteristic constant groaning in late stage progressive supranuclear palsy: a case report.. PARKINSONISM & RELATED DISORDERS, 17 (7), 575-576. doi:10.1016/j.parkreldis.2011.04.015
Plazzi, G., Pizza, F., Palaia, V., Franceschini, C., Poli, F., Moghadam, K.K., ...Dauvilliers, Y. (2011). Complex movement disorders at disease onset in childhood narcolepsy with cataplexy. BRAIN, 134 3477-3489. doi:10.1093/brain/awr244
Ruge, D., Tisch, S., Hariz, M.I., Zrinzo, L., Bhatia, K.P., Quinn, N.P., ...Rothwell, J.C. (2011). Deep brain stimulation effects in dystonia: time course of electrophysiological changes in early treatment.. MOVEMENT DISORDERS, 26 (10), 1913-1921. doi:10.1002/mds.23731
Moretto, G., Schwingenschuh, P., Katschnig, P., Bhatia, K.P., Haggard, P. (2011). Delayed experience of volition in Gilles de la Tourette syndrome.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 82 (12), 1324-1327. doi:10.1136/jnnp.2010.221143
Spencer, C.C.A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., ...Blackburn, H. (2011). Dissection of the genetics of Parkinson's disease identifies an additional association 5 ' of SNCA and multiple associated haplotypes at 17q21. HUMAN MOLECULAR GENETICS, 20 (2), 345-353. doi:10.1093/hmg/ddq469
Spencer, C.C.A., Plagnol, V., Strange, A., Gardner, M., Paisan-Ruiz, C., Band, G., ...Blackburn, H. (2011). Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Human Molecular Genetics, 20 (2), 345-353. doi:10.1093/hmg/ddq469
Rubio-Agusti, I., Carecchio, M., Lachman, R., Edwards, M., Bhatia, K., Murphy, E. (2011). Dystonia in adult patients with classical galactosemia.
Albanese, A., Asmus, F., Bhatia, K.P., Elia, A.E., Elibol, B., Filippini, G., ...Newton, A. (2011). EFNS guidelines on diagnosis and treatment of primary dystonias.. EUROPEAN JOURNAL OF NEUROLOGY, 18 (1), 5-18. doi:10.1111/j.1468-1331.2010.03042.x
Moreno-Lopez, C., Santamaria, J., Salamero, M., Del Sorbo, F., Albanese, A., Pellecchia, M.T., ...Aarden, W. (2011). Excessive Daytime Sleepiness in Multiple System Atrophy (SLEEMSA Study). ARCHIVES OF NEUROLOGY, 68 (2), 223-230. doi:10.1001/archneurol.2010.359
Kassavetis, P., Parees, I., Saifee, T.A., Davare, M., Bhatia, K.P., Edwards, M.J. (2011). Explicit versus implicit motor learning in psychogenic movement disorders.
Mian, O.S., Schneider, S.A., Schwingenschuh, P., Bhatia, K.P., Day, B.L. (2011). Gait in SWEDDs patients: Comparison with Parkinson's disease patients and healthy controls. Movement Disorders, 26 (7), 1266-1273. doi:10.1002/mds.23684
Mian, O.S., Schneider, S.A., Schwingenschuh, P., Bhatia, K.P., Day, B.L. (2011). Gait in SWEDDs patients: comparison with Parkinson's disease patients and healthy controls.. MOVEMENT DISORDERS, 26 (7), 1266-1273. doi:10.1002/mds.23684
Schneider, S.A., Ramirez, A., Shafiee, K., Kaiser, F.J., Erogullari, A., Brüggemann, N., ...Shafa, M.A. (2011). Homozygous THAP1 mutations as cause of early-onset generalized dystonia.. MOVEMENT DISORDERS, 26 (5), 858-861. doi:10.1002/mds.23561
Schneider, S.A., Bhatia, K.P. (2011). Huntington's disease look-alikes.. Handbook of Clinical Neurology, 100 101-112. doi:10.1016/B978-0-444-52014-2.00005-7
Edwards, M.J., Bhatia, K.P., Cordivari, C. (2011). Immediate response to botulinum toxin injections in patients with fixed dystonia.. MOVEMENT DISORDERS, 26 (5), 917-918. doi:10.1002/mds.23562
Nalls, M.A., Plagnol, V., Hernandez, D.G., Sharma, M., Sheerin, U.-.M., Saad, M., ...Sveinbjornsdottir, S. (2011). Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. LANCET, 377 (9766), 641-649. doi:10.1016/S0140-6736(10)62345-8
Kojovic, M., Bologna, M., Kassavetis, P., Murase, N., Berardelli, A., Rothwell, J.C., ...Bhatia, K.P. (2011). INCREASED CORTICAL MOTOR PLASTICITY AND PRESERVED INTRACORTICAL INHIBITION ON THE LESS AFFECTED SIDE OF EARLY ASYMMETRIC DRUG NAIVE PARKINSON'S DISEASE PATIENTS.
Parees, I., Kassavetis, P., Saifee, T.A., Bhatia, K.P., Edwards, M.J. (2011). Jumping to conclusions in psychogenic movement disorders patients.
Katschnig, P., Massano, J., Edwards, M.J., Schwingenschuh, P., Cordivari, C., Bhatia, K.P. (2011). Late-onset asymmetric myoclonus: an emerging syndrome.. MOVEMENT DISORDERS, 26 (9), 1744-1748. doi:10.1002/mds.23676
Shiner, T., Seymour, B., Hill, C., Dayan, P., Bhatia, K., Dolan, R. (2011). Learning and Performance in Parkinson's Disease.
Shiner, T., Seymour, B., Hill, C., Dayan, P., Bhatia, K., Dolan, R. (2011). Learning and performance in Parkinson's disease.
Edwards, M.J., Alonso-Canovas, A., Schrag, A., Bloem, B.R., Thompson, P.D., Bhatia, K. (2011). Limb amputations in fixed dystonia: a form of body integrity identity disorder?. MOVEMENT DISORDERS, 26 (8), 1410-1414. doi:10.1002/mds.23671
Kassavetis, P., Edwards, M.J., Parees, I., Saifee, T.A., Bhatia, K.P., Cordivari, C. (2011). Long-term effectiveness of botulinum toxin injections treating psychogenic movement disorders.
Parees, I., Saifee, T.A., Kassavetis, P., Kojovic, M., Rubio-Agusti, I., Bhatia, K.P., Edwards, M.J. (2011). Mismatch between tremor self report and long-term actigraphy in psychogenic tremor.
Mir, P., Trender-Gerhard, I., Edwards, M.J., Schneider, S.A., Bhatia, K.P., Jahanshahi, M. (2011). Motivation and movement: the effect of monetary incentive on performance speed.. EXPERIMENTAL BRAIN RESEARCH, 209 (4), 551-559. doi:10.1007/s00221-011-2583-5
Moustris, A., Edwards, M.J., Bhatia, K.P. (2011). Movement disorders and mitochondrial disease.. Handbook of Clinical Neurology, 100 173-192. doi:10.1016/B978-0-444-52014-2.00010-0
Rubio-Agusti, I., Carecchio, M., Lachmann, R., Edwards, M.J., Murphy, E., Bhatia, K.P. (2011). Movement disorders in adult patients with classical galactosemia.
Carecchio, M., Schneider, S.A., Chan, H., Lachmann, R., Lee, P.J., Murphy, E., Bhatia, K.P. (2011). Movement disorders in adult surviving patients with maple syrup urine disease.. MOVEMENT DISORD, 26 (7), 1324-1328. doi:10.1002/mds.23629
Carecchio, M., Schneider, S.A., Chan, H., Lee, P.J., Lachmann, R., Murphy, E., Bhatia, K.P. (2011). Movement disorders in adult-surviving patients with maple syrup urine disease.
Stamelou, M., Edwards, M.J., Espay, A.J., Fung, V.S.C., Hallett, M., Lang, A.E., ...Bhatia, K.P. (2011). Movement Disorders on YouTube - Caveat Spectator. NEW ENGLAND JOURNAL OF MEDICINE, 365 (12), 1160-1161. doi:10.1056/NEJMc1107673
Schwingenschuh, P., Katschnig, P., Seiler, S., Saifee, T., Aguirregomozcorta, M., Schmidt, R., ...Edwards, M. (2011). Moving towards "laboratory supported" criteria for psychogenic tremor.
Schwingenschuh, P., Katschnig, P., Seiler, S., Saifee, T., Aguirregomozcorta, M., Schmidt, R., ...Edwards, M.J. (2011). Moving towards 'laboratory supported' criteria for psychogenic tremor.
Kojovic, M., Cordivari, C., Bhatia, K. (2011). Myoclonic disorders: a practical approach for diagnosis and treatment.. Therapeutic Advances in Neurological Disorders, 4 (1), 47-62. doi:10.1177/1756285610395653
Bhatia, K. (2011). Neurodegeneration with brain iron accumulation disorders: an update.
Edwards, M.J., Bhatia, K.P. (2011). Other Non-Motor Symptoms of Parkinson's Disease. In Parkinson's Disease: Non-Motor and Non-Dopaminergic Features. (pp. 387-393). .
Madhusudanan, M., Bhatia, K.P., Balint, B. (2011). Paroxysmal craniocervical dyskinesia as manifestation of frontal lobe epilepsy. MOVEMENT DISORDERS, 26 (14), 2580-2582. doi:10.1002/mds.23925
Bhatia, K.P. (2011). Paroxysmal dyskinesias.. MOVEMENT DISORDERS, 26 (6), 1157-1165. doi:10.1002/mds.23765
Katschnig, P., Schwingenschuh, P., Chaudhary, U.J., Edwards, M.J., Lemieux, L., Walker, M.C., Bhatia, K.P. (2011). Paroxysmal limb dyskinesia induced by weight: an unusual case of cortical reflex seizures.. MOVEMENT DISORDERS, 26 (13), 2438-2439. doi:10.1002/mds.23874
Hoffland, B.S., Snik, D., Bhatia, K.P., Baratelli, E., Katschnig, P., Schwingenschuh, P., ...Edwards, M.J. (2011). Patients with primary cervical dystonia have evidence of discrete deficits in praxis. Journal of Neurology, Neurosurgery and Psychiatry, 82 (6), 615-619. doi:10.1136/jnnp.2010.221937
Pizza, F., Palaia, V., Franceschini, C., Poli, F., Moghadam, K.K., Mignot, E., ...Plazzi, G. (2011). PERSISTENT HYPOTONIA WITH COMPLEX MOVEMENT DISORDER IN CHILDHOOD NARCOLEPSY-CATAPLEXY AT DISEASE ONSET.
Schneider, S.A., Bhatia, K.P. (2011). Recognition of Faciobrachial Dystonic Seizures Allowing Early Intervention with and Prevention of Development of Full-Blown Limbic Encephalitis. MOVEMENT DISORDERS, 26 (12), 2176. doi:10.1002/mds.23963
Albanese, A., Asmus, F., Bhatia, K., Elia, A.E., Elibol, B., Filippini, G., ...Newton, A. (2011). Response to letter by Dr Neil Murray.. EUROPEAN JOURNAL OF NEUROLOGY, 18 (6), E62. doi:10.1111/j.1468-1331.2010.03346.x
Schwingenschuh, P., Katschnig, P., Edwards, M.J., Teo, J.T.H., Korlipara, L.V.P., Rothwell, J.C., Bhatia, K.P. (2011). The blink reflex recovery cycle differs between essential and presumed psychogenic blepharospasm.. NEUROLOGY, 76 (7), 610-614. doi:10.1212/WNL.0b013e31820c3074
Damásio, J., Edwards, M.J., Alonso-Canovas, A., Schwingenschuh, P., Kägi, G., Bhatia, K.P. (2011). The clinical syndrome of primary tic disorder associated with dystonia: A large clinical series and a review of the literature.. MOVEMENT DISORDERS, 26 (4), 679-684. doi:10.1002/mds.23484
Damásio, J., Edwards, M.J., Alonso-Canovas, A., Schwingenschuh, P., Kägi, G., Bhatia, K.P. (2011). The clinical syndrome of primary tic disorder associated with dystonia: a large clinical series and a review of the literature.. Movement disorders : official journal of the Movement Disorder Society, 26 (4), 679-684. doi:10.1002/mds.23484
Shiner, T., Seymour, B., Symmonds, M., Dayan, P., Bhatia, K., Dolan, R. (2011). The Effect of Motivation on Movement: A Study of Bradykinesia in Parkinson's Disease.
Shiner, T., Seymour, B., Symmonds, M., Dayan, P., Bhatia, K., Dolan, R. (2011). The effect of motivation on movement: A study of bradykinesia in Parkinson's disease.
Griffin, H.J., Greenlaw, R., Limousin, P., Bhatia, K., Quinn, N.P., Jahanshahi, M. (2011). The effect of real and virtual visual cues on walking in Parkinson's disease.. JOURNAL OF NEUROLOGY, 258 (6), 991-1000. doi:10.1007/s00415-010-5866-z
Rubio-Agusti, I., Carecchio, M., Edwards, M., Bhatia, K., Lachmann, R., Murphy, E. (2011). THE SPECTRUM OF MOVEMENT DISORDERS IN ADULT PATIENTS WITH CLASSICAL GALACTOSEMIA. JOURNAL OF INHERITED METABOLIC DISEASE, 34 S177.
Bhatia, K.P. (2011). The Wilson films--Wilson's disease.. MOVEMENT DISORDERS, 26 (14), 2473-2474. doi:10.1002/mds.24037
Saifee, T.A., Parees, I., Kassavetis, P., Kaski, D., Bronstein, A.M., Bhatia, K.P., ...Edwards, M.J. (2011). Tremor in Charcot Marie Tooth disease.
Quinn, N.P., Schneider, S.A., Schwingenschuh, P., Bhatia, K.P. (2011). Tremor-Some Controversial Aspects. MOVEMENT DISORDERS, 26 (1), 18-23. doi:10.1002/mds.23289
Quinn, N.P., Schneider, S.A., Schwingenschuh, P., Bhatia, K.P. (2011). Tremor-some controversial aspects.. Movement Disorders, 26 (1), 18-23. doi:10.1002/mds.23289
Quinn, N.P., Schneider, S.A., Schwingenschuh, P., Bhatia, K.P. (2011). Tremor--some controversial aspects.. Movement disorders : official journal of the Movement Disorder Society, 26 (1), 18-23. doi:10.1002/mds.23289
Murase, N., Farmer, S.F., Rothwell, J.C., Bhatia, K. (2011). Unilateral-dominant activation of the primary motor cortex on the side of well-developed contralateral corticospinal tract in congenital mirror movement without other neurological abnormalities.
Kojovic, M., Sheerin, U.M., Wood, N., Houlden, H., Hardy, J., Bhatia, K.P. (2011). Young onset parkinsonism due to alpha synuclein gene multiplication in a consanguineous family - A case report.

2010

Kojovic, M., Kuoppamäki, M., Quinn, N., Bhatia, K.P. (2010). "Progressive delayed-onset postanoxic dystonia" diagnosed with PANK2 mutations 26 years after onset-an update.. MOVEMENT DISORDERS, 25 (16), 2889-2891. doi:10.1002/mds.23153
Steindl, K., Alazami, A.M., Bhatia, K.P., Wuerfel, J.T., Petersen, D., Cartolari, R., ...Alkuraya, F.S. (2010). A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome.. CLINICAL GENETICS, 78 (6), 594-597. doi:10.1111/j.1399-0004.2010.01447.x
Schneider, S.A., Wilkinson, L., Bhatia, K.P., Henley, S.M.D., Rothwell, J.C., Tabrizi, S.J., Jahanshahi, M. (2010). Abnormal explicit but normal implicit sequence learning in premanifest and early Huntington's disease.. Movement Disorders, 25 (10), 1343-1349.
Schwingenschuh, P., Katschnig, P., Saurugg, R., Ott, E., Bhatia, K.P. (2010). Artistic profession: a potential risk factor for dopamine dysregulation syndrome in Parkinson's disease?. MOVEMENT DISORDERS, 25 (4), 493-496. doi:10.1002/mds.22936
Schneider, S.A., Paisan-Ruiz, C., Quinn, N.P., Lees, A.J., Houlden, H., Hardy, J., Bhatia, K.P. (2010). ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation.. MOVEMENT DISORDERS, 25 (8), 979-984. doi:10.1002/mds.22947
Alonso-Canovas, A., Katschnig, P., Tucci, A., Carecchio, M., Wood, N.W., Edwards, M., ...Bhatia, K.P. (2010). Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: case report and literature review.. MOVEMENT DISORDERS, 25 (10), 1506-1509. doi:10.1002/mds.23109
Alonso-Canovas, A., Katschnig, P., Tucci, A., Carecchio, M., Wood, N., Edwards, M., ...Bhatia, K. (2010). Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease: Expanding the spectrum.
Kojovic, M., Caronni, A., Bologna, M., Rothwell, J., Bhatia, K., Edwards, M. (2010). Botulinum toxin injections reduce cortical plasticity in cervical dystonia.
Draganski, B., Bhatia, K.P. (2010). Brain structure in movement disorders: a neuroimaging perspective. CURRENT OPINION IN NEUROLOGY, 23 (4), 413-419. doi:10.1097/WCO.0b013e32833bc59c
Alazami, A.M., Schneider, S.A., Bonneau, D., Pasquier, L., Carecchio, M., Kojovic, M., ...Bhatia, K.P. (2010). C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.. CLINICAL GENETICS, 78 (6), 585-590. doi:10.1111/j.1399-0004.2010.01441.x
Carecchio, M., Fenoglio, C., Benussi, L., Ghidoni, R., Cantoni, C., Serpente, M., ...Monaco, F. (2010). Cerebrospinal fluid biomarkers in patients carrying delCACT mutation in exon 8 of Progranulin gene: report of 10 Italian cases.
Parees, I., Kojovic, M., Bhatia, K. (2010). Cervical dystonia associated with facioscapulohumeral dystrophy: expanding the clinical spectrum.
Schneider, S.A., Lang, A.E., Moro, E., Bader, B., Danek, A., Bhatia, K.P. (2010). Characteristic head drops and axial extension in advanced chorea-acanthocytosis.. MOVEMENT DISORDERS, 25 (10), 1487-1491. doi:10.1002/mds.23052
Carecchio, M., Bonetti, M., Magliozzi, M., Edwards, M.J., Ferraris, A., Torrente, I., ...Bhatia, K. (2010). Defining the phenotypic signature of DYT11 mutations in myoclonus-dystonia patients.
Albanese, A., Asmus, F., Berardelli, A., Bhatia, K., Elia, A.E., Elibol, B., ...Nardocci, N. (2010). Diagnosis and Treatment of Primary (Idiopathic) Dystonia. In European Handbook of Neurological Management: Second Edition. (pp. 191-206). .
Schwingenschuh, P., Ruge, D., Edwards, M.J., Terranova, C., Katschnig, P., Carrillo, F., ...Palomar, F.J. (2010). Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: a clinical and electrophysiological study.. MOVEMENT DISORDERS, 25 (5), 560-569. doi:10.1002/mds.23019
Moore, J.W., Schneider, S.A., Schwingenschuh, P., Moretto, G., Bhatia, K.P., Haggard, P. (2010). Dopaminergic medication boosts action-effect binding in Parkinson's disease. Neuropsychologia,
Schneider, S.A., Bhatia, K.P. (2010). DYT10, Paroxysmal Kinesiogenic Dyskinesia-PKD. In Encyclopedia of Movement Disorders. (pp. 429-431). .
Schneider, S.A., Bhatia, K.P. (2010). DYT8, Paroxysmal Non-kinesiogenic Dyskinesia-PNKD. In Encyclopedia of Movement Disorders. (pp. 424-426). .
Schneider, S.A., Bhatia, K.P. (2010). DYT9, Paroxysmal Dyskinesia with Spasticity. In Encyclopedia of Movement Disorders. (pp. 427-428). .
Paisán-Ruiz, C., Guevara, R., Federoff, M., Hanagasi, H., Sina, F., Elahi, E., ...Emre, M. (2010). Early-onset L-dopa-responsive Parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and Spatacsin mutations. Movement Disorders, 25 (12), 1791-1800. doi:10.1002/mds.23221
Paisán-Ruiz, C., Guevara, R., Federoff, M., Hanagasi, H., Sina, F., Elahi, E., ...Emre, M. (2010). Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.. MOVEMENT DISORDERS, 25 (12), 1791-1800. doi:10.1002/mds.23221
Mayahi, L., Mason, L., Bleasdale-Barr, K., Donald, A., Trender-Gerhard, I., Sweeney, M.G., ...Watson, L. (2010). Endothelial, Sympathetic, and Cardiac Function in Inherited (6R)-L-Erythro-5,6,7,8-Tetrahydro-L-Biopterin Deficiency. CIRCULATION-CARDIOVASCULAR GENETICS, 3 (6), 513-522. doi:10.1161/CIRCGENETICS.110.957605
Pavese, N., Moore, R.Y., Scherfler, C., Khan, N.L., Hotton, G., Quinn, N.P., ...Lees, A.J. (2010). In vivo assessment of brain monoamine systems in parkin gene carriers: a PET study.. EXPERIMENTAL NEUROLOGY, 222 (1), 120-124. doi:10.1016/j.expneurol.2009.12.021
Aggarwal, A., Schneider, S.A., Houlden, H., Silverdale, M., Paudel, R., Paisan-Ruiz, C., ...Hardy, J. (2010). Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms.. MOVEMENT DISORDERS, 25 (10), 1424-1431. doi:10.1002/mds.23095
Baratelli, E., Edwards, M., Carecchio, M., Jarman, P.R., Heales, S.J.R., Bhatia, K.P. (2010). Juvenile onset dystonia-parkinsonism associated with cerebral folate deficiency.
Carecchio, M., Collini, A., Comi, C., Cantello, R., Bhatia, K.P., Monaco, F. (2010). Levodopa-Induced Belly Dancer's Dyskinesias in Parkinson's Disease: Report of One Case. MOVEMENT DISORDERS, 25 (11), 1760-1762. doi:10.1002/mds.23345
Filipovic, S.R., Rothwell, J.C., Bhatia, K. (2010). Low-frequency repetitive transcranial magnetic stimulation and off-phase motor symptoms in Parkinson's disease. JOURNAL OF THE NEUROLOGICAL SCIENCES, 291 (1-2), 1-4. doi:10.1016/j.jns.2010.01.017
Katschnig, P., Edwards, M.J., Schwingenschuh, P., Aguirregomozcorta, M., Kaegi, G., Rothwell, J.C., Bhatia, K.P. (2010). Mental rotation of body parts and sensory temporal discrimination in fixed dystonia.
Katschnig, P., Edwards, M.J., Schwingenschuh, P., Aguirregomozcorta, M., Kägi, G., Rothwell, J.C., Bhatia, K.P. (2010). Mental rotation of body parts and sensory temporal discrimination in fixed dystonia.. MOVEMENT DISORDERS, 25 (8), 1061-1067. doi:10.1002/mds.23047
Schneider, S.A., Pleger, B., Draganski, B., Cordivari, C., Rothwell, J.C., Bhatia, K.P., Dolan, R. (2010). Modulatory effects of 5Hz rTMS over the primary somatosensory cortex in focal dystonia - an fMRI-TMS study.
Schneider, S.A., Pleger, B., Draganski, B., Cordivari, C., Rothwell, J.C., Bhatia, K.P., Dolan, R.J. (2010). Modulatory effects of 5Hz rTMS over the primary somatosensory cortex in focal dystonia--an fMRI-TMS study.. MOVEMENT DISORDERS, 25 (1), 76-83. doi:10.1002/mds.22825
Schwingenschuh, P., Katschnig, P., Aguirregomozcorta, M., Saifee, T., Lunn, M.P., Manji, H., ...Edwards, M.J. (2010). Neurophysiological evidence for cerebellar dysfunction in neuropathic tremor.
Saifee, T., Schwingenschuh, P., Katschnig, P., Aguirregomozcorta, M., Bhatia, K.P., Rothwell, J., ...Edwards, M.J. (2010). Neurophysiological evidence for cerebellar dysfunction in neuropathic tremor.
Kaegi, G., Klein, C., Wood, N.W., Schneider, S.A., Pramstaller, P.P., Tadic, V., ...Bhatia, K.P. (2010). Nonmotor Symptoms in Parkin Gene-Related Parkinsonism. MOVEMENT DISORDERS, 25 (9), 1279-1284. doi:10.1002/mds.22897
Carecchio, M., Rahman, S., Hanna, M.G., Heales, S., Hargreaves, I., Land, J., Bhatia, K. (2010). Parkinsonism, multiple lipomas and hearing impairment in a patient with reduced activity of mitochondrial respiratory chain complexes II plus III.
Rosenzweig, I., Bhatia, K.P., Nashef, L., Brunnhuber, F. (2010). Paroxysmal Dyskinesia With Deja Vu Aura. JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES, 22 (1), E9-E10.
Rosenzweig, I., Bhatia, K.P., Nashef, L., Brunnhuber, F. (2010). Paroxysmal dyskinesia with déjà vu aura.. Journal of Neuropsychiatry and Clinical Neurosciences, 22 (1), doi:10.1176/appi.neuropsych.22.1.123-f.e9
Bhatia, K.P., Schneider, S. (2010). Paroxysmal dyskinesias. In Movement Disorders 4. (pp. 489-505). Saunders.
Hoffland, B.S., Snik, D., Baratelli, E., Katschnig, P., Schwingenschuh, P., Bhatia, K.P., ...Edwards, M.J. (2010). Patients with primary cervical dystonia have evidence of deficits in praxis.
Schneider, S.A., Bhatia, K.P. (2010). Rare causes of dystonia parkinsonism.. CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS, 10 (6), 431-439. doi:10.1007/s11910-010-0136-0
Aguirregomozcorta, M., Edwards, M.J., Schwingenschuh, P., Prvulovich, E., Quinn, N.P., Dickson, J.C., Bhatia, K.P. (2010). Scans with ipsilateral dopaminergic deficit (SW/DDs): A new entity.
Schneider, S.A., Bhatia, K.P. (2010). Secondary dystonia - clinical clues and syndromic associations.
Filipovic, S.R., Rothwell, J.C., Bhatia, K. (2010). Slow (1 Hz) repetitive transcranial magnetic stimulation (rTMS) induces a sustained change in cortical excitability in patients with Parkinson's disease. CLINICAL NEUROPHYSIOLOGY, 121 (7), 1129-1137. doi:10.1016/j.clinph.2010.01.031
Del Sorbo, F., Schneider, S., Bhatia, K.P. (2010). SNCA Variants Are Associated with Increased Risk for Multiple System Atrophy(vol 65, pg 610, 2009). ANNALS OF NEUROLOGY, 67 (2), 277. doi:10.1002/ana.22013
Bhatia, K., Frydenberg, E., Steel, T., Ow-Yang, M., Ho, K., Grainger, E. (2010). Spinal epidural lipomatosis due to a bronchial ACTH-secreting carcinoid tumour. Journal of Clinical Neuroscience, 17 (11), 1461-1462. doi:10.1016/j.jocn.2010.04.008
Houlden, H., Schneider, S.A., Paudel, R., Melchers, A., Schwingenschuh, P., Edwards, M., ...Bhatia, K.P. (2010). THAP1 mutations (DYT6) are an additional cause of early-onset dystonia.. NEUROLOGY, 74 (10), 846-850. doi:10.1212/WNL.0b013e3181d5276d
Edwards, M.J., Schwingenschuh, P., Katschnig, P., Teo, J., Korlipara, L., Rothwell, J.C., Bhatia, K. (2010). The Blink Reflex Recovery Cycle Differs between Patients with Benign Essential Blepharospasm and Patients with Atypical (Presumed Psychogenic) Blepharospasm.
Schwingenschuh, P., Katschnig, P., Teo, J.T., Edwards, M.J., Rothwell, J.C., Bhatia, K.P. (2010). The blink reflex recovery cycle distinguishes patients with benign essential blepharospasm from patients with presumed psychogenic blepharospasm.
Valadas, A., Damasio, J., Edwards, M.J., Bhatia, K.P. (2010). The clinical expression of psychogenic facial movement disorders.
Damasio, J., Edwards, M.J., Alonso-Canovas, A., Schwingenschuh, P., Bhatia, K.P. (2010). The entity of primary tic disorder associated with dystonia: a large clinical series.
Kägi, G., Bhatia, K.P., Tolosa, E. (2010). The role of DAT-SPECT in movement disorders.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 81 (1), 5-12. doi:10.1136/jnnp.2008.157370
Schneider, S.A., Bhatia, K.P. (2010). Three Faces of the Same Gene: FA2H Links Neurodegeneration with Brain Iron Accumulation, Leukodystrophies, and Hereditary Spastic Paraplegias. ANNALS OF NEUROLOGY, 68 (5), 575-577. doi:10.1002/ana.22211
Katschnig, P., Schwingenschuh, P., Edwards, M.J., Bhatia, K.P. (2010). Unilateral cortical myoclonus.
Snik, D., Sofie Hoffland, B., Aguirregomozcorta, M., Schwingenschuh, P., Bhatia, K.P., van de Warrenburg, B.P., Edwards, M.J. (2010). Validation of a dystonia screening questionnaire: testing in a cohort of mixed neurological disorders.. PARKINSONISM & RELATED DISORDERS, 16 (9), 620-622. doi:10.1016/j.parkreldis.2010.07.003
Aguirregomozcorta, M., Edwards, M.J., Prvulovich, E., Schneider, S.A., Quinn, N.P., Lees, A.J., ...Bhatia, K.P. (2010). Why do clinicians request DaT scans? An analysis of requesting practice and outcome in 455 consecutive scans.

2009

Li, A., Paisan-Ruiz, C., Holton, J.L., Schneider, S., Hardy, J., Kidd, D., ...Revesz, T. (2009). A pathological genotype-phenotype study of four neuroaxonal dystrophy cases with PLA2G6 mutations.
Schneider, S.A., Wilkinson, L., Bhatia, K.P., Henley, S., Rothwell, J., Tabrizi, S.J., Jahanshahi, M. (2009). Abnormal explicit but intact implicit sequence learning in presymptomatic and early Huntington's disease. MOVEMENT DISORDERS, 24 S169.
Schippling, S., Schneider, S.A., Bhatia, K.P., Münchau, A., Rothwell, J.C., Tabrizi, S.J., Orth, M. (2009). Abnormal motor cortex excitability in preclinical and very early Huntington's disease.. Biological Psychiatry, 65 (11), 959-965. doi:10.1016/j.biopsych.2008.12.026
Quartarone, A., Rizzo, V., Terranova, C., Morgante, F., Schneider, S., Ibrahim, N., ...Rothwell, J.C. (2009). Abnormal sensorimotor plasticity in organic but not in psychogenic dystonia. Brain,
Mian, O.S., Schneider, S.A., Schwingenschuh, P., Bhatia, K.P., Day, B.L. (2009). Are parkinsonian gait characteristics present in patients with SWEDDs?.
Trender-Gerhard, I., Sweeney, M.G., Schwingenschuh, P., Mir, P., Edwards, M.J., Gerhard, A., ...Wood, N.W. (2009). Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients. Journal of Neurology, Neurosurgery and Psychiatry, 80 (8), 839-845. doi:10.1136/jnnp.2008.155861
Foltynie, T., Cheeran, B., Williams-Gray, C.H., Edwards, M.J., Schneider, S.A., Weinberger, D., ...Bhatia, K.P. (2009). BDNF val66met influences time to onset of levodopa induced dyskinesia in Parkinson's disease. Journal of Neurology, Neurosurgery and Psychiatry, 80 (2), 141-144. doi:10.1136/jnnp.2008.154294
Thompson, P.D. (2009). Case Study 23. In Parkinsonian Disorders in Clinical Practice. (pp. 175-179). .
Sleiman, P.M., Healy, D.G., Muqit, M.M., Yang, Y.X., van der, B.M., Holton, J.L., ...Diss, J.K. (2009). Characterisation of a novel NR4A2 mutation in Parkinson's disease brain. Neuroscience Letters, 457 (2), 75-79. doi:10.1016/j.neulet.2009.03.021
Paisan-Ruiz, C., Bhatia, K.P., Li, A., Hernandez, D., Davis, M., Wood, N.W., ...Schneider, S.A. (2009). Characterization of PLA2G6 as a locus for Dystonia-Parkinsonism. Annals of Neurology, 65 (1), 19-23. doi:10.1002/ana.21415
Schwingenschuh, P., Ruge, D., Edwards, M.J., Terranova, C., Carrillo, F., Schneider, S.A., ...Dickson, J. (2009). Clinical and Electrophysiological Parameters Can Differentiate Patients with SWEDDs from Tremor-Dominant Parkinson's Disease.
Carecchio, M., Comi, C., Varrasi, C., Stecco, A., Sainaghi, P.P., Bhatia, K., ...Monaco, F. (2009). Complex movement disorders in primary anti phospholipid syndrome: A case report. Journal of the Neurological Sciences, 281 (1-2), 101-103. doi:10.1016/j.jns.2009.03.011
Schneider, S.A., Bhatia, K.P., Hardy, J. (2009). Complicated recessive dystonia parkinsonism syndromes. Movement Disorders, 24 (4), 490-498. doi:10.1002/mds.22314
Farrer, M.J., Hulihan, M.M., Kachergus, J.M., Dachsel, J.C., Stoessl, A.J., Grantier, L.L., ...Chapon, F. (2009). DCTN1 mutations in Perry syndrome. Nature Genetics, 41 (2), 163-165. doi:10.1038/ng.293
Schwingenschuh, P., Saurugg, R., Katschnig, P., Ott, E., Bhatia, K.P. (2009). Dopaminergic addiction to increase artistic creativity.
Moore, J.W., Susanne, S.A., Schwingenschuh, P., Moretto, G., Bhatia, K.P., Haggard, P. (2009). Dopaminergic medication exaggerates the experience of voluntary motor control in Parkinson's disease.
Martinez-Torres, I., Limousin, P., Tisch, S., Page, R., Pinto, A., Foltynie, T., ...Zrinzo, L. (2009). Early and marked benefit with GPi DBS for Lubag syndrome presenting with rapidly progressive life-threatening dystonia.. Mov Disord, 24 1710–2. doi:10.1002/mds.22656
Unterhalter, E. (2009). Editorial introduction. Unknown, 653-654.
Healy, D.G., Bressman, S., Dickson, J., Silveira-Moriyama, L., Schneider, S.A., O'Sullivan, S.S., ...Bomanji, J. (2009). Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-Ataxia syndrome. Movement Disorders, 24 (8), 1245-1247. doi:10.1002/mds.22267
Griffin, H.J., Greenlaw, R., Limousin, P., Bhatia, K., Quinn, N.P., Jahanshahi, M. (2009). External cueing and gait in Parkinson's disease: A controlled evaluation.
Aguirregomozcorta, M., Schwingenschuh, P., Katschnig, P., Paisan-Ruiz, C., Wood, N., Bhatia, K. (2009). Familial adult-onset tremulous segmental dystonia associated with epilepsy, a new phenotype?.
Draganski, B., Schneider, S.A., Fiorio, M., Klöppel, S., Gambarin, M., Tinazzi, M., ...Frackowiak, R.S.J. (2009). Genotype-phenotype interactions in primary dystonias revealed by differential changes in brain structure.. NEUROIMAGE, 47 (4), 1141-1147. doi:10.1016/j.neuroimage.2009.03.057
Schneider, S.A., Paisan-Ruiz, C., Garcia-Gorostiaga, I., Quinn, N.P., Weber, Y.G., Lerche, H., ...Bhatia, K.P. (2009). GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias. Movement Disorders, 24 (11), 1684-1688. doi:10.1002/mds.22507
Schneider, S.A.S., Paisan-Ruiz, C., Garcia-Gorostiaga, I., Quinn, N.P., Weber, Y., Lerche, H., ...Bhatia, K.P. (2009). GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.
Weber, Y.G., Storch, A., Wuttke, T.V., Brockmann, K., Kempfle, J., Maljevic, S., ...Huber, S.M. (2009). GLUT1 MUTATIONS IN PATIENTS WITH PAROXYSMAL EXERTION-INDUCED DYSKINESIA.
Esposito, M., Edwards, M.J., Bhatia, K.P., Toms, N.J., Allen, P.J., Brown, P., Cordivari, C. (2009). Idiopathic spinal myoclonus: A clinical and neurophysiological assessment of a movement disorder of uncertain origin.
Esposito, M., Edwards, M.J., Bhatia, K.P., Brown, P., Cordivari, C. (2009). Idiopathic spinal myoclonus: a clinical and neurophysiological assessment of a movement disorder of uncertain origin.. MOVEMENT DISORDERS, 24 (16), 2344-2349. doi:10.1002/mds.22812
Schneider, S.A., Hardy, J., Bhatia, K.P. (2009). Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2: causative or consequential?. Journal of Neurology, Neurosurgery and Psychiatry, 80 (6), 589-590. doi:10.1136/jnnp.2008.169953
Ruge, D., Tisch, S., Limousin, P., Hariz, M.I., Bhatia, K.P., Quinn, N., ...Rothwell, J.C. (2009). Longitudinal effects of deep brain stimulation in the globus pallidus on intracortical GABAergic inhibition and LTP-like plasticity in dystonia.
Healy, D.G., Sullivan, S.O., Bonifati, V., Durr, A., Bressman, S., Brice, A., ...Tolosa, E. (2009). LRRK2 ASSOCIATED PARKINSON'S DISEASE: CLINICAL FACTORS BASED ON WORLDWIDE EXPERIENCE.
Quinn, N., Bhatia, K., Brown, P., Cordivari, C., Hariz, M., Lees, A., ...Tabrizi, S. (2009). Movement disorders. In Clarke, C., Howard, R., Rossor, M., Shorvon, S. (Eds.), Neurology: a Queen Square textbook. (pp. 155-187). Chichester: Wiley-Blackwell.
Lang, A.E., Angel, M., Bhatia, K., Chen, R., Fahn, S., Hallett, M., ...Thompson, P. (2009). Myoclonus in Complex Regional Pain Syndrome. MOVEMENT DISORDERS, 24 (2), 314-316. doi:10.1002/mds.22355
Teo, J.T.H., van de Warrenburg, B.P.C., Schneider, S.A., Rothwell, J.C., Bhatia, K.P. (2009). Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia. Journal of Neurology, Neurosurgery and Psychiatry, 80 (1), 80-83. doi:10.1136/jnnp.2008.144626
Pavese, N., Khan, N.L., Scherfler, C., Cohen, L., Brooks, D.J., Wood, N.W., ...Piccini, P. (2009). Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: an 18F-dopa PET progression study.. MOVEMENT DISORDERS, 24 (15), 2260-2266. doi:10.1002/mds.22817
van der Salm, S.M.A., van Rootselaar, A.F., Foncke, E.M.J., Koelman, J.H.T.M., Bour, L.J., Bhatia, K.P., ...Tijssen, M.A.J. (2009). Normal cortical excitability in Myoclonus-Dystonia--a TMS study.. Exp.Neurol., 216 (2), 300-305.
Silveira-Moriyama, L., Schwingenschuh, P., O'Donnell, A., Schneider, S.A., Mir, P., Carrillo, F., ...Quinn, N.P. (2009). Olfaction in patients with suspected parkinsonism and scans without evidence of dopaminergic deficit (SWEDDs). Journal of Neurology, Neurosurgery and Psychiatry, 80 (7), 744-748. doi:10.1136/jnnp.2009.172825
Katschnig, P., Schwingenschuh, P., Edwards, M., Walker, M., Bhatia, K. (2009). Paroxysmal unilateral cortical arm myoclonus induced by holding a weight.
Katschnig, P., Schwingenschuh, P., Walker, M., Bhatia, K.P. (2009). Paroxysmal unilateral cortical myoclonus induced by holding a weight.
Li, A., Paisan-Ruiz, C., Bhatia, K., Schneider, S., Hardy, J., Kidd, D., ...Revesz, T. (2009). Pathological observations in seven cases with neurodegeneration with brain iron accumulation (NBIA) with mutations in PANK2 and PLA2G6.
Kaegi, G., Katschnig, P., Fiorio, M., Tinazzi, M., Rothwell, J., Bhatia, K. (2009). Patients with adult-onset cervical dystonia and marked improvement to a sensory trick perform better in multimodal temporal discrimination.
Carrillo, F., Schneider, S.A., Taylor, A.M.R., Srinivasan, V., Kapoor, R., Bhatia, K.P. (2009). Prominent oromandibular dystonia and pharyngeal telangiectasia in atypical ataxia telangiectasia. Cerebellum, 8 (1), 22-27. doi:10.1007/s12311-008-0055-7
Schneider, S.A., Udani, V., Sawant, C., Bhatia, K.P. (2009). Recurrent acute dystonic reaction and oculogyric crisis despite withdrawal of dopamine receptor blocking drugs.
Schneider, S.A., Udani, V., Sankhla, C.S., Bhatia, K.P. (2009). Recurrent acute dystonic reaction and oculogyric crisis despite withdrawal of dopamine receptor blocking drugs. Movement Disorders, 24 (8), 1226-1229. doi:10.1002/mds.22532
Filipovic, S.R., Rothwell, J.C., van de Warrenburg, B.P., Bhatia, K. (2009). Repetitive transcranial magnetic stimulation for levodopa-induced dyskinesias in Parkinson's disease. Mov Disord., 24 (2), 246-253.
Edwards, M.J., Bhatia, K.P. (2009). Reply: Puschmann "Unverricht-Lundborg disease-A misnomer". Movement Disorders, 24 (4), 630. doi:10.1002/mds.22118
De Grandis, E., Mir, P., Edwards, M.J., Bhatia, K.P. (2009). Restless legs may be associated with the post-polio syndrome. Parkinsonism and Related Disorders, 15 (1), 74-75. doi:10.1016/j.parkreldis.2008.02.005
Schneider, S.A., Bhatia, K.P. (2009). Secondary dystonia-clinical clues and syndromic associations.. Journal of movement disorders, 2 (2), 58-63. doi:10.14802/jmd.09016
Tinazzi, M., Fiorio, M., Fiaschi, A., Rothwell, J.C., Bhatia, K.P. (2009). Sensory functions in dystonia: insights from behavioral studies. Movement Disorders, 24 (10), 1427-1436. doi:10.1002/mds.22490
Tinazzi, M., Fiorio, M., Fiaschi, A., Rothwell, J.C., Bhatia, K.P. (2009). Sensory functions in dystonia: insights from behavioral studies. 24 (10), 1427-1436.
Katschnig, P., Kagi, G., Schwingenschuh, P., Rothwell, J.C., Bhatia, K.P. (2009). Sensory temporal discrimination and mental rotation of corporal objects in patients with early-onset parkinsonism, positive or negative fur mutations in the parkin gene, compared to healthy controls.
Katschnig, P., Kagi, G., Schwingenschuh, P., Rothwell, J.C., Bhatia, K.P. (2009). Sensory-temporal discrimination and mental rotation of corporal objects in patients with early-onset parkinsonism, positive or negative for mutations in the Parkin gene, compared to healthy controls.
Scholz, S.W., Houlden, H., Schulte, C., Sharma, M., Li, A., Berg, D., ...Simon-Sanchez, J. (2009). SNCA Variants Are Associated with Increased Risk for Multiple System Atrophy. ANNALS OF NEUROLOGY, 65 (5), 610-614. doi:10.1002/ana.21685
Schwingenschuh, P., Katschnig, P., Teo, J.T., Edwards, M.J., Korlipara, P., Rothwell, J.C., Bhatia, K.P. (2009). The blink reflex recovery cycle differs between patients with benign essential blepharospasm and patients with atypical (presumed psychogenic) blepharospasm.
Ibrahim, N.M., Martino, D., van de Warrenburg, B.P.C., Quinn, N.P., Bhatia, K.P., Brown, R.J., ...Schrag, A. (2009). The prognosis of fixed dystonia: a follow-up study.. PARKINSONISM & RELATED DISORDERS, 15 (8), 592-597. doi:10.1016/j.parkreldis.2009.02.010
Czerny, J., Cordivari, C., Schwingenschuh, P., Esposito, M., Bhatia, K.P. (2009). The smiling tremor.
Kojovic, M., Edwards, M., Schneider, S., Bitner, M., Valente, E.M., Bhatia, K. (2009). The syndrome of deafness-dystonia - a case series of 11 patients.
Kojovic, M., Edwards, M.J., Schneider, S., Bitner, M., Valente, E.M., Bhatia, K.P. (2009). The syndrome of deafness-dystonia - A case series of 11 patients.
Schwingenschuh, P., Katschnig, P., Lunn, M.P., Manji, H., Bhatia, K.P., Reilly, M.M., Edwards, M.J. (2009). Tremor in immune-mediated neuropathies.
Schwingenschuh, P., Katschnig, P., Aguirregomozcorta, M., Lunn, M.P., Manji, H., Bhatia, K.P., ...Edwards, M.J. (2009). Tremor in immune-mediated neuropathies.
Schwingenschuh, P., Cordivari, C., Czerny, J., Esposito, M., Bhatia, K.P. (2009). Tremor on smiling. Movement Disorders, 24 (10), 1542-1545. doi:10.1002/mds.22666
Obeso, J.A., Jahanshahi, M., Alvarez, L., Macias, R., Pedroso, I., Wilkinson, L., ...Rodríguez-Oroz, M.C. (2009). What can man do without basal ganglia motor output? The effect of combined unilateral subthalamotomy and pallidotomy in a patient with Parkinson's disease. Experimental Neurology, 220 (2), 283-292. doi:10.1016/j.expneurol.2009.08.030

2008

Martino, D., Bhatia, K.P. (2008). A case of intermittent chorea induced by coffee. In Movement Disorders 100 Instructive Cases. CRC Press.
Cheeran, B., Talelli, P., Mori, F., Koch, G., Suppa, A., Edwards, M., ...Rothwell, J.C. (2008). A common polymorphism in the brain-derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS. The Journal of Physiology, 586 (23), 5717-5725. doi:10.1113/jphysiol.2008.159905
Tinazzi, M., Simonetto, S., Franco, L., Bhatia, K.P., Moretto, G., Fiaschi, A., Deluca, C. (2008). Abduction finger sign: a new sign to detect unilateral functional paralysis of the upper limb.. MOVEMENT DISORDERS, 23 (16), 2415-2419. doi:10.1002/mds.22268
Schwingenschuh, P., Terranova, C., Carrillo, F., Schneider, S., Kagi, G., Edwards, M.J., ...Mir, P. (2008). Adult onset dystonia can cause tremulous pseudoparkinsoniasm and is one cause of SWEDDs: Clinical description of 30 cases.
Schwingenschuh, P., Terranova, C., Carrillo, F., Schneider, S., Kagi, G., Edwards, M.J., ...Mir, P. (2008). Adult onset dystonia can cause tremulous pseudoparkinsoniasm and is one cause of SWEDDs: Clinical description of 30 cases.
Koch, G., Schneider, S., Baumer, T., Franca, M., Munchau, A., Cheeran, B., ...Caltagirone, C. (2008). Altered dorsal premotor-motor interhemispheric pathway activity in focal arm dystonia. Movement Disorders, 23 (5), 660-668. doi:10.1002/mds.21881
van de Warrenburg, B.P.C., Church, A.J., Martino, D., Candler, P.M., Bhatia, K.P., Giovannoni, G., Quinn, N.P. (2008). Antineuronal antibodies in Parkinson's disease. Movement Disorders, 23 (7), 958-963. doi:10.1002/mds.21929
Kagi, G., Schwingenschuh, P., Bhatia, K.P. (2008). Arm swing is reduced in adult onset primary cervical dystonia.
Kagi, G., Schwingenschuh, P., Bhatia, K.P. (2008). Arm swing is reduced in adult onset primary cervical dystonia.
Kagi, G., Schwingenschuh, P., Bhatia, K.P. (2008). Arm swing is reduced in idiopathic cervical dystonia. Movement Disorders, 23 (12), 1784-1787. doi:10.1002/mds.22216
Trender-Gerhard, I., Sweeney, M.G., Schwingenschuh, P., Mir, P., Edwards, M.J., Gerhard, A., ...Bhatia, K.P. (2008). Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome in 34 patients.
Foltynie, T., Cheeran, B., Williams-Gray, C.H., Edwards, M.J., Schneider, S.A., Weinberger, D., ...Bhatia, K.P. (2008). BDNF val66met influences time to onset of levodopa-induced dyskinesia in Parkinson's disease.
Foltynie, T., Cheeran, B., Williams-Gray, C.H., Edwards, M.J., Schneider, S.A., Weinberger, D., ...Bhatia, K.P. (2008). BDNF val66met influences time to onset of levodopa-induced dyskinesia in Parkinson's disease.
Schwingenschuh, P., Ruge, D., Terranova, C., Edwards, M.J., Schneider, S.A., Silveira-Moriyama, L., ...Bhatia, K.P. (2008). Certain tremor parameters can differentiate PD tremor from pseudoparkinsonian tremor in patients with normal DAT scans (SWEDDs).
Schwingenschuh, P., Ruge, D., Terranova, C., Edwards, M.J., Schneider, S.A., Silveira-Moriyama, L., ...Bhatia, K.P. (2008). Certain tremor parameters can differentiate PD tremor from pseudoparkinsonian tremor in patients with normal DAT scans (SWEDDs).
Paisan-Raiz, C., Bhatia, K.P., Li, A., Hernandez, D., Davis, M., Wood, N., ...Schneider, S.A. (2008). Characterisation of PLA2G6 as a locus for dystonia-parkinsonism.
Paisan-Ruiz, C., Bhatia, K.P., Li, A., Hernandez, D., Davis, M., Wood, N., ...Schneider, S.A. (2008). Characterisation of PLA2G6 as a locus for dystonia-parkinsonism.
Schwingenschuh, P., Ruge, D., Terranova, C., Carrillo, F., Schneider, S.A., Kagi, G., ...Rothwell, J. (2008). Clinical and electrophysiological criteria to differentiate patients with dystonic tremulous pseudo-parkinsonism from tremor-dominant Parkinson's disease.
Tisch, S., Rothwell, J.C., Zrinzo, L., Bhatia, K.P., Hariz, M., Limousin, P. (2008). Cortical evoked potentials from pallidal stimulation in patients with primary generalized dystonia. Mov Disord, 23 265–73. doi:10.1002/mds.21835
Avanzino, L., Martino, D., van de Warrenburg, B.P., Schneider, S.A., Abbruzzese, G., Defazio, G., ...Rothwell, J.C. (2008). Cortical excitability is abnormal in patients with the "fixed dystonia" syndrome. Movement Disorders, 23 (5), 646-652. doi:10.1002/mds.21801
Farrer, M.J., Hulihan, M.M., Kachergus, J., Stoessl, A.J., Grantier, L.L., Daechsel, J., ...Calne, D.B. (2008). DCTN1 mutations in families with parkinsonism, depression, weight loss and central hypoventilation: Perry syndrome.
Schneider, S.A., Walker, R.H., Bhatia, K.P. (2008). Differential diagnosis of chorea.
Schneider, S.A., Bhatia, K.P. (2008). Dystonia in the Woodhouse Sakati svndrome - a new family and literature review.
Schneider, S.A., Bhatia, K.P. (2008). Dystonia in the Woodhouse Sakati syndrome - a new family and literature review.
Schneider, S.A., Bhatia, K.P. (2008). Dystonia in the Woodhouse Sakati syndrome - A new family and literature review.
Schneider, S.A., Bhatia, K.P. (2008). Dystonia in the Woodhouse Sakati syndrome: A new family and literature review. Movement Disorders, 23 (4), 592-596. doi:10.1002/mds.21886
Schneider, S.A., Robertson, M.M., Rizzo, R., Turk, J., Bhatia, K.P., Orth, M. (2008). Fragile X syndrome associated with tic disorders. Movement Disorders, 23 (8), 1108-1112. doi:10.1002/mds.21995
Weber, Y.G., Storch, A., Wuttke, T.V., Brockmann, K., Kempfle, J., Maljevic, S., ...Huber, S.M. (2008). GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak. Journal of Clinical Investigation, 118 (6), 2157-2168. doi:10.1172/JCI34438
Wild, E.J., Mudanohwo, E.E., Sweeney, M.G., Schneider, S.A., Beck, J., Bhatia, K.P., ...Tabrizi, S.J. (2008). Huntington's disease phenocopies are clinically and genetically heterogeneous. Movement Disorders, 23 (5), 716-720. doi:10.1002/mds.21915
Filipovic, S.R., Heywood, P., Rothwell, J.C., de Warrenburgh, B., Bhatia, K. (2008). Low frequency repetitive transcranial magnetic stimulation reduces levodopa induced diphasic dyskinesias in Parkinson's disease: A case report.
Schneider, S.A., Talelli, P., Cheeran, B.J., Khan, N.L., Wood, N.W., Rothwell, J.C., Bhatia, K.P. (2008). Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations. Movement Disorders, 23 (13), 1812-1819. doi:10.1002/mds.22025
Alazami, A.M., Al-Saif, A., Al-Semari, A., Bohlega, S., Zlitni, S., Alzahrani, F., ...Khalak, H. (2008). Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. The American Journal of Human Genetics, 83 (6), 684-691. doi:10.1016/j.ajhg.2008.10.018
Holton, J.L., Schneider, S.A., Ganesharajah, T., Gandhi, S., Strand, C., Shashidharan, P., ...Bhatia, K.P. (2008). Neuropathology of primary adult onset non-DYT1 dystonia.
Holton, J.L., Schneider, S.A., Ganesharajah, T., Gandhi, S., Strand, C., Shashidharan, P., ...Bhatia, K.P. (2008). Neuropathology of primary adult-onset dystonia. Neurology, 70 (9), 695-699. doi:10.1212/01.wnl.0000302175.76229.f0
Holton, J.L., Schneider, S.A., Gandhi, S., Ganesharajah, T., Strand, C., Shashidharan, P., ...Bhatia, K.P. (2008). Neuropathology of primary dystonia unrelated to DYT1 mutations.
Teo, J.T.H., van de Warrenburg, B.P.C., Schneider, S.A., Rothwell, J.C., Bhatia, K.P. (2008). Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia.
Teo, J.T.H., van de Warrenburg, B.P.C., Schneider, S.A., Rothwell, J.C., Bhatia, K.P. (2008). Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia.
Kagi, G., Klein, C., Wood, N.W., Schneider, S.A., Pramstaller, P.P., Tadic, V., ...Bhatia, K.P. (2008). Non-motor symptoms in parkin gene-related parkinsonism.
Kagi, G., Klein, C., Wood, N.W., Schneider, S.A., Pramstaller, P.P., Tudic, V., ...Bhatia, K.P. (2008). Non-motor symptoms in parkin gene-related parkinsonism.
Schwingenschuh, P., Bhatia, K.P. (2008). Painful moving tongue in a patient with the painful legs moving toes syndrome. Movement Disorders, 23 (9), 1324-1325. doi:10.1002/mds.22160
Edwards, M., Quinn, N., Bhatia, K. (2008). Parkinson's disease and other movement disorders. Oxford: Oxford University Press.
De Grandis, E., Mir, P., Edwards, M.J., Quinn, N.P., Bhatia, K.P. (2008). Paroxysmal dyskinesia with interictal myoclonus and dystonia: A report of two cases. Parkinsonism and Related Disorders, 14 (3), 250-252. doi:10.1016/j.parkreldis.2007.03.005
Schwingenschuh, P., Schneider, S.A., Terranova, C., Edwards, M., Dickson, J., Silveira-Moriyama, L., ...Bhatia, K. (2008). Patients with adult onset dystonic tremor and scans without evidence of dopaminergic deficit (SWEDDs) resembiling tremulous Parkinson's Disease: A comparative analysis of 21 cases.
Healy, D.G., Falchi, M., O'Sullivan, S.S., Bonifati, V., Durr, A., Bressman, S., ...Goldwurm, S. (2008). Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. The Lancet Neurology, 7 (7), 583-590. doi:10.1016/S1474-4422(08)70117-0
Van De Warrenburg, B.P.C., Bhatia, K.P., Quinn, N.P. (2008). Pisa syndrome after unilateral pallidotomy in Parkinson's disease: An unrecognised, delayed adverse event? (Journal of Neurology, Neurosurgery and Psychiatry (2007) 78, (329-330)). Journal of Neurology, Neurosurgery and Psychiatry, 79 (3), 337-. doi:10.1136/jnnp.2006.103358corr1
Paisan-Ruiz, C., Bhatia, K.P., Li, A., Hernandez, D., Davis, M., Wood, N., ...Schneider, S.A. (2008). PLA2G6 as a locus for adult-onset dystonia-parkinsonism.
Schwingenschuh, P., Ruge, D., Terranova, C., Schneider, S.A., Mir, P., Rothwell, J.C., ...Edwards, M.J. (2008). Plasticity of sensorimotor circuits in patients with SWEDDs resembles the pattern seen in dystonia and differs from Parkinson's disease.
Schwingenschuh, P., Ruge, D., Terranova, C., Schneider, S.A., Mir, P., Rothwell, J.C., ...Edwards, M.J. (2008). Plasticity of sensorimotor circuits in patients with SWEDDs resembles the pattern seen in dystonia and differs from Parkinson's disease.
Teo, J.T.H., Schneider, S.A., Cheeran, B.J., Fernandez-Del-Olmo, M., Guinti, P., Rothwell, J.C., Bhatia, K.P. (2008). Prolonged cortical silent period but normal sensorimotor plasticity in spinocerebellar ataxia 6.
Teo, J.T.H., Schneider, S.A., Cheeran, B.J., Fernandez-del-Olmo, M., Guinti, P., Rothwell, J.C., Bhatia, K.P. (2008). Prolonged cortical silent period but normal sensorimotor plasticity in spinocerebellar ataxia 6.
Schwingenschuh, P., Pont-Sunyer, C., Surtees, R., Bhatia, K.P. (2008). Psychogenic movement disorders in children: A report of 15 cases and a review of the literature.
Schwingenschuh, P., Pont-Sunyer, C., Surtees, R., Bhatia, K.P. (2008). Psychogenic movement disorders in children: A report of 15 cases and a review of the literature.
Schwingenschuh, P., Pont-Sunyer, C., Surtees, R., Edwards, M.J., Bhatia, K.P. (2008). Psychogenic movement disorders in children: A report of 15 cases and a review of the literature. Movement Disorders, 23 (13), 1882-1888. doi:10.1002/mds.22280
Cheeran, B.J., Talelli, P., Mori, F., Koch, G., Schneider, S.A., Suppa, A., ...Rothwell, J.C. (2008). Stimulation genomics: Identifying functional polymorphisms modulating LTP and LTD in human cerebral cortex and implications for levodopa induced dyskinesia in Parkinson's disease (PD).
Cheeran, B.J., Talelli, P., Mori, F., Koch, G., Schneider, S.A., Suppa, A., ...Rothwell, J.C. (2008). Stimulation genomics: Identifying functional polymorphisms modulating LTP and LTD in human cerebral cortex and implications for levodopa induced dyskinesia in Parkinson's disease (PD).
Cano, S.J., Warner, T.T., Thompson, A.J., Bhatia, K.P., Fitzpatrick, R., Hobart, J.C. (2008). The cervical dystonia impact profile (CDIP-58): can a Rasch developed patient reported outcome measure satisfy traditional psychometric criteria?. Health and Quality of Life Outcomes, 6 58-. doi:10.1186/1477-7525-6-58
Chew, N.K., Mir, P., Edwards, M.J., Cordivari, C., Martino, D., Schneider, S.A., ...Bhatia, K.P. (2008). The natural history of Unverricht-Lundborg disease: A report of eight genetically proven cases. Movement Disorders, 23 (1), 107-113. doi:10.1002/mds.21812
Kagi, G., Bhatia, K.P., Tolosa, E. (2008). The role of DAT-SPECT in movement disorders.
Silverdale, M.A., Schneider, S.A., Bhatia, K.P., Lang, A.E. (2008). The spectrum of orolingual tremor--a proposed classification system.. MOVEMENT DISORDERS, 23 (2), 159-167. doi:10.1002/mds.21776
Talelli, P., van de Warrenburg, B.P.C., Schneider, S.A., Edwards, M.J., Giunti, P., Wood, N.W., ...Bhatia, K.P. (2008). The syndrome of cervical dystonia-cerebellar ataxia (DYTCA): Dystonia without loss of cortical inhibition.
Talelli, P., van de Warrenburg, B.P.C., Schneider, S.A., Edwards, M.J., Giunti, P., Wood, N.W., ...Bhatia, K.P. (2008). The syndrome of cervical dystonia-cerebellar ataxia (DYTCA): Dystonia without loss of cortical inhibition.
Koukouni, V., Valente, E.M., Cordivari, C., Bhatia, K.P., Quinn, N.P. (2008). Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp. Movement Disorders, 23 (13), 1913-1915. doi:10.1002/mds.21935

2007

Schwingenschuh, P., Schneider, S., Silveira-Moriyama, L., Kaegi, G., Terranova, C., Mir, P., ...Lees, A. (2007). Adult onset dystonic tremor as differential diagnosis for Parkinson's disease: Detailed clinical description of 20 patients emphasizing non-motor symptoms including olfactory function.
Schwingenschuh, P., Schneider, S., Silveira-Moriyama, L., Kaegi, G., Terranova, C., Mir, P., ...Lees, A. (2007). Adult onset dystonic tremor as differential diagnosis for Parkinson's disease: Detailed clinical description of 20 patients emphasizing non-motor symptoms including olfactory function.
Khan, N.L., Bhatt, M., Brooks, D.J., Korlipara, P., Schapira, A., Piccini, P., ...Bhatia, K. (2007). An Indian kindred with reversible dystonia and parkinsonism.
Quartarone, A., Rizzo, V., Terranova, C., Schneider, S.A., Morgante, F., Girlanda, P., ...Rothwell, J.C. (2007). Associative plasticity in psychogenic dystonia.
Kim, H.T., Edwards, M.J., Tyson, J., Quinn, N.P., Bitner-Glindzicz, M., Bhatia, K.P. (2007). Blepharospasm and limb dystonia caused by Mohr-Tranebjaerg syndrome with a novel splice-site mutation in the deafness/dystonia peptide gene. Movement Disorders, 22 (9), 1328-1331.
Fiorio, M., Stanzani, C., Rothwell, J.C., Bhatia, K.P., Moretto, G., Fiaschi, A., Tinazzi, M. (2007). Defective temporal discrimination of passive movements in Parkinson's disease.. NEUROSCIENCE LETTERS, 417 (3), 312-315. doi:10.1016/j.neulet.2007.02.050
Fiorio, M., Gambarin, M., Valente, E.M., Liberini, P., Loi, M., Cossu, G., ...Aglioti, S.M. (2007). Defective temporal processing of sensory stimuli in DYT1 mutation carriers: a new endophenotype of dystonia?. Brain, 130 (1), 134-142. doi:10.1093/brain/awl283
Edwards, M.J., Bhatia, K.P. (2007). Drug-induced and tardive dystonia. In Warner, T.T., Bressman, S.B. (Eds.), Clinical diagnosis and management of dystonia. (pp. 149-158). London: Informa healthcare.
Warner, T.T. (2007). Dystonia. In Schapira, A.H.V. (Ed.), Neurology and Clinical Neurosciences. (pp. 443-454). Philadelphia: Mosby Elsevier.
Tisch, S., Zrinzo, L., Limousin, P., Bhatia, K.P., Quinn, N., Ashkan, K., Hariz, M. (2007). Effect of electrode contact location on clinical efficacy of pallidal deep brain stimulation in primary generalised dystonia. J Neurol Neurosurg Psychiatr, 78 1314–9. doi:10.1136/jnnp.2006.109694
Cano, S.J., Thompson, A., Bhatia, K., Fitzpatrick, R., Warner, T.T., Hobart, J.C. (2007). Evidence-based guidelines for using the Short Form 36 in cervical dystonia.. Movement Disorders, 22 (1), 122-127.
Schneider, S.A., Robertson, M.M., Rizzo, R., Turk, J., Bhatia, K.P., Orth, M. (2007). Fragile X syndrome associated with tic disorders.
Tisch, S., Ruge, D., Limousin, P., Hariz, M., Bhatia, K.P., Quinn, N.P., ...Rothwell, J.C. (2007). Longitudinal effects of pallidal stimulation on motor cortex function in dystonia.
Fiorio, M., Tinazzi, M., Ionta, S., Fiaschi, A., Moretto, G., Edwards, M.J., ...Aglioti, S.M. (2007). Mental rotation of body parts and non-corporeal objects in patients with idiopathic cervical dystonia.. NEUROPSYCHOLOGIA, 45 (10), 2346-2354. doi:10.1016/j.neuropsychologia.2007.02.005
Holton, J.L., Schneider, S.A., Gandhi, S., Ganesharajah, T., Strand, C., Shashidharan, P., ...Bhatia, K.P. (2007). Neuropathology of primary dystonia unrelated to DYT1 mutations.
Yogarajah, M., Wilkins, A., Bhatia, K., Jarman, P. (2007). New insight into the mechanisms underling chorea in polycythaemia vera: A case report.
Tisch, S., Rothwell, J.C., Bhatia, K.P., Quinn, N., Zrinzo, L., Jahanshahi, M., ...Limousin, P. (2007). Pallidal stimulation modifies after-effects of paired associative stimulation on motor cortex excitability in primary generalised dystonia. Experimental Neurology, 206 (1), 80-85. doi:10.1016/j.expneurol.2007.03.027
van de Warrenburg, B.P.C., Rodriguez-Justo, M., Vella, N.R., Freeman, A., Bhatia, K.P., Quinn, N.P. (2007). Paraneoplastic cerebellar ataxia due to burnt-out testicular germ cell tumour?. European Neurology, 57 (3), 178-181.
Mir, P., Schneider, S.A., Bhatia, K.P. (2007). Paroxysmal dyskinesias. In Warner, T.T., Bressman, S.B. (Eds.), Clinical diagnosis and management of dystonia. (pp. 159-170). London: Informa healthcare.
Schneider, S.A., Edwards, M.J., Mir, P., Cordivari, C., Hooker, J., Dickson, J., ...Bhatia, K.P. (2007). Patients with adult-onset dystonic tremor resembling parkinsonian tremor have scans without evidence of dopaminergic deficit (SWEDDs). Movement Disorders, 22 (15), 2210-2215. doi:10.1002/mds.21685
van de Warrenburg, B.P., Cordivari, C., Brown, P., Bhatia, K.P. (2007). Persisting hyperekplexia after idiopathic, self-limiting brainstem encephalopathy. Movement Disorders, 22 (7), 1017-1020.
Draganski, B., Schneider, S.A., Stefan, K., Bhatia, K.P., Frackowiak, R.S.J. (2007). Phenotype and genotype driven changes of basal ganglia structure in primary dystonia.
van de Warrenburg, B.P.C., Bhatia, K.P., Quinn, N.P. (2007). Pisa syndrome after unilateral pallidotomy in Parkinson's disease: an unrecognised, delayed adverse event?. Journal of Neurology, Neurosurgery and Psychiatry, 78 (3), 329-330. doi:10.1136/jnnp.2006.103358
Norlinah, I.M., Bhatia, K.P., Ostergaard, K., Howard, R., Arabia, G., Quinn, N.P. (2007). Primary lateral sclerosis mimicking atypical parkinsonism. Movement Disorders, 22 (14), 2057-2062. doi:10.1002/mds.21645
Koukouni, V., Bhatia, K.P. (2007). Psychogenic parkinsonism. In Koller, W.C., Melamed, E. (Eds.), Parkinson's disease and related disorders, part II. (pp. 501-506). Edinburgh: Elsevier.
Bhatia, K.P., Schneider, S.A. (2007). Psychogenic tremor and related disorders. Journal of Neurology, 254 (5), 569-574. doi:10.1007/s00415-006-0348-z
Schneider, S.A., Bhatia, K.P. (2007). The entitity of jaw tremor and dystonia.
Schneider, S.A., Bhatia, K.P. (2007). The entity of jaw tremor and dystonia. Movement Disorders, 22 (10), 1491-1495.
Koukouni, V., Martino, D., Arabia, G., Quinn, N.P., Bhatia, K.P. (2007). The entity of young onset primary cervical dystonia. Movement Disorders, 22 (6), 843-847. doi:10.1002/mds.21421
Schneider, S.A., Walker, R.H., Bhatia, K.P. (2007). The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test. Nature Clinical Practice Neurology, 3 (9), 517-525. doi:10.1038/ncpneuro0606
van de Warrenburg, B.P.C., Cordivari, C., Ryan, A.M., Phadke, R., Holton, J.L., Bhatia, K.P., ...Quinn, N.P. (2007). The phenomenon of disproportionate antecollis in Parkinson's disease and multiple system atrophy. Movement Disorders, 22 (16), 2325-2331. doi:10.1002/mds.21634
Silverdale, M.A., Schneider, S.A., Bhatia, K.P., Lang, A.E. (2007). The spectrum of orolingual tremor - a proposed classification system.
Talelli, P., van de Warrenburg, B.P.C., Schneider, S.A., Giunti, P., Quinn, N.P., Wood, N.W., ...Bhatia, K.P. (2007). The syndrome of dystonia and cerebellar ataxia: Cortical excitability and pathophysiological implications.
van der Salm, S.M.A., van Rootselaar, A.-.F., Foncke, E.M.J., Koelman, J.T.H.M., Bour, L.J., Bhatia, K.P., ...Thijssen, M.A.J. (2007). Transcranial magnetic stimulation in myoclonus-dystonia.

2006

Abou-Sleiman, P.M., Muqit, M.M.K., McDonald, N.Q., Gandhi, S., Healy, D.G., Harvey, K., ...Lees, A.J. (2006). A heterozygous effect for PINK1 mutations in Parkinson's disease; low frequency low penetrance?. Annals of Neurology, 60 (4), 414-419. doi:10.1002/ana.20960
Healy, D., Muqit, M., Abu Sleiman, P., Yang, Y., Holton, J., Revesz, T., ...Andrew, L. (2006). A novel 5'UTR mutation of Nurr1 reduces Nurr1 expression in Parkinson's disease brain in vivo.
Albanese, A., Barnes, M.P., Bhatia, K.P., Fernandez-Alvarez, E., Filippini, G., Gasser, T., ...Savoiardo, M. (2006). A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force.. EUROPEAN JOURNAL OF NEUROLOGY, 13 (5), 433-444. doi:10.1111/j.1468-1331.2006.01537.x
Huang, Y., Edwards, M.J., Rothwell, J.C., Bhatia, K.P. (2006). Abnormal blink reflex recovery cycle in manifesting and non-manitesting carriers of the DYT1 gene mutation.
Avanzino, L., Martino, D., Schneider, S., van de Warrenburg, B., Defazio, G., Abbruzzese, G., ...Rothwell, J. (2006). Abnormal cortical excitability in patients with the "fixed dystonia" syndrome.
Edwards, M.J., Huang, Y.Z., Mir, P., Rothwell, J.C., Bhatia, K.P. (2006). Abnormalities in motor cortical plasticity differentiate manifesting and nonmanifesting DYT1 carriers. Movement Disorders, 21 (12), 2181-2186. doi:10.1002/mds.21160
Bhatia, K.P., Schneider, S.A., Edwards, M.J., Hooker, J., Mir, P., Dickson, J., ...Quinn, N.P. (2006). Adult onset dystonic tremor with similarities to Parkinsonian tremor may be one cause of SWEDDS.
Schneider, S.A., Edwards, M.J., Grill, S.E., Goldstein, S., Kanchana, S., Quinn, N.P., ...Reich, S.G. (2006). Adult-onset primary lower limb dystonia. Movement Disorders, 21 (6), 767-771.
Mir, P., Gilio, F., Edwards, M., Inghilleri, M., Bhatia, K.P., Rothwell, J.C., Quinn, N. (2006). Alteration of central motor excitability in a patient with hemimasticatory spasm after treatment with botulinum toxin injections. Movement Disorders, 21 (1), 73-78.
Martino, D., Chew, N.K., Mir, P., Edwards, M.J., Quinn, N.P., Bhatia, K.P. (2006). Atypical movement disorders in antiphospholipid syndrome. Movement Disorders, 21 (7), 944-949. doi:10.1002/mds.20842
Schneider, S.A., Edwards, M.J., Cordivari, C., MacLeod, W.N., Bhatia, K.P. (2006). Botulinum toxin A may be efficacious as treatment for jaw tremor in Parkinson's disease. Movement Disorders, 21 (10), 1722-1724.
Schneider, S.A., Edwards, M.J., Cordivari, C., Macleod, W., Bhatia, K.P. (2006). Botulinum toxin is effective in the treatment of Parkinson jaw tremor.
Cano, S.J., Hobart, J.C., Edwards, M., Fitzpatrick, R., Bhatia, K., Thompson, A.J., Warner, T.T. (2006). CDIP-58 can measure the impact of botulinum toxin treatment in cervical dystonia.. Neurology, 67 (12), 2230-2232. doi:10.1212/01.wnl.0000249310.25427.f2
Tisch, S., Limousin, P., Rothwell, J.C., Asselman, P., Quinn, N., Jahanshahi, M., ...Hariz, M. (2006). Changes in blink reflex excitability after globus pallidus internus stimulation for dystonia. Movement Disorders, 21 (10), 1650-1655.
Tisch, S., Limousin, P., Rothwell, J.C., Asselman, P., Zrinzo, L., Jahanshahi, M., ...Hariz, M.I. (2006). Changes in forearm reciprocal inhibition following pallidal stimulation for dystonia. Neurology, 66 1091–3. doi:10.1212/01.wnl.0000204649.36458.8f
Tisch, S., Zrinzo, L., Hariz, M., Quinn, N., Bhatia, K.P., Rothwell, J.C., Limousin, P. (2006). Cortical evoked potentials from stimulation of globus pallidus in patients with primary generalised dystonia. EUROPEAN JOURNAL OF NEUROLOGY, 13 221.
Talelli, P., Schneider, S.A., Cheeran, B.J., Kahn, N.N., Wood, N.W., Rothwell, J.C., Bhatia, K.P. (2006). Corticospinal and intracortical excitability in patients and asymptomatic carriers with parkin gene mutations: A TMS study.
Mayahi, L., Mason, L., Storry, C., Donald, A., Trender-Gherhard, I., Mathias, C., ...Pellerin, D. (2006). Endothelial, sympathetic and cardiac function in inherited 6R-L-Erythro-5,6,7,8-Tetrahydro-L-Biopterin deficiency. Circulation, 114 (18), 283.
Schneider, S.A., Mohire, M.D., Trender-Gerhard, I., Asmus, F., Sweeney, M., Mary, D., ...Bhatia, K.P. (2006). Familial dopa-responsive cervical dominant dystonia.
Schneider, S.A., Mohire, M.D., Trender-Gerhard, I., Asmus, F., Sweeney, M., Davis, M., ...Bhatia, K.P. (2006). Familial dopa-responsive cervical dystonia. Neurology, 66 (4), 599-601.
Schneider, S.A., Bhatia, K.P. (2006). Historical landmarks in the elucidation of DRD - Did it exist before Segawa's description?.
Gerhard, A., Trender-Gerhard, I., Turkheimer, F., Quinn, N.P., Bhatia, K.P., Brooks, D.J. (2006). In vivo imaging of microglial activation with [C-11](R)-PK11195 PET in progressive supranuclear palsy. Movement Disorders, 21 (1), 89-93.
Koch, G., Schneider, S., Baumer, T., Franca, M., Munchau, A., Cheeran, B., ...Rothwell, J.C. (2006). Interhemispheric inhibition of the dorsal premotor-motor pathway is reduced in writer's cramp dystonia.
Bhatia, K.P., Schneider, S.A. (2006). Is the anticonvulsant topiramate beneficial in essential tremor?. Nature Clinical Practice Neurology, 2 (9), 478-479.
Huang, Y.Z., Trender-Gerhard, I., Edwards, M.J., Mir, P., Rothwell, J.C., Bhatia, K.P. (2006). Motor system inhibition in dopa-responsive dystonia and its modulation by treatment. Neurology, 66 (7), 1088-1090.
Koukouni, V., Cordivari, C., Bhatia, K.P., Quinn, N.P. (2006). Myoclonus dystonia due to e-sarcoglycane gene mutation presenting with falls. EUROPEAN JOURNAL OF NEUROLOGY, 13 91.
Healy, D.G., Abou-Sleiman, P.M., Ahmadi, K.R., Gandhi, S., Muqit, M.M., Bhatia, K.P., ...Revesz, T. (2006). NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach. Movement Disorders, 21 (11), 1960-1963. doi:10.1002/mds.21018
Schneider, S.A., van de Warrenburg, B.P.C., Hughes, T.D., Davis, M., Sweeney, M., Wood, N., ...Bhatia, K.P. (2006). Phenotypic homogeneity of the Huntington disease - like presentation in a SCA17 family. Neurology, 67 (9), 1701-1703.
Schneider, S.A., van de Warrenburg, B.A., Hughes, T.D., Davis, M., Sweeney, M., Wood, N., ...Bhatia, K.P. (2006). Phenotypic homogeneity of the Huntington's disease-like presentation in a SCA17 family.
Defazio, G., Martino, D., Aniello, M.S., Masi, G., Gigante, A., Bhatia, K., ...Berardelli, A. (2006). Planning genetic studies on primary adult-onset dystonia: Sample size estimates based on examination of first-degree relatives. JOURNAL OF THE NEUROLOGICAL SCIENCES, 251 (1-2), 29-34. doi:10.1016/j.jns.2006.08.009
Ibrahim, M., Bhatia, K.P., Ostergaard, K., Arabia, G., Quinn, N.P. (2006). Primary lateral sclerosis mimicking atypical parkinsonian syndrome: A challenging early diagnosis.
Medcalf, P., Bhatia, K.P. (2006). Restless legs syndrome. BMJ (Clinical Research Ed.), 333 (7566), 457-459A.
Cordivari, C., Misra, V.P., Vincent, A., Catania, S., Bhatia, K.P., Lees, A.J. (2006). Secondary nonresponsiveness to botulinum toxin a in cervical dystonia: The role of electromyogram-guided injections, botulinum toxin a antibody assay, and the extensor digitorum brevis test. Movement Disorders, 21 (10), 1737-1741.
Schneider, S.A., Aggarwal, A., Bhatt, M., Dupont, E., Tisch, S., Limousin, P., ...Bhatia, K.P. (2006). Severe tongue protrusion dystonia: clinical syndromes and possible treatment. Neurology, 67 (6), 940-943.
Schneider, S.A., Aggarwal, A., Bhatt, M., Dupont, E., Tisch, S., Limousin, P., ...Bhatia, K.P. (2006). Severe tongue protrusion dystonia: clinical syndromes and their management.
Tinazzi, M., Fiorio, M., Stanzani, C., Moretto, G., Smania, N., Fiaschi, A., ...Rothwell, J.C. (2006). Temporal discrimination of two passive movements in writer's cramp. Movement Disorders, 21 (8), 1131-1135.
Tisch, S., Hariz, M., Bhatia, K.P., Quinn, N., Zrinzo, L., Jahanshahi, M., ...Limousin, P. (2006). The effect of pallidal stimulation on motor cortex plasticity in primary generalised dystonia.
Koukouni, V., Martino, D., Arabia, G., Quinn, N.P., Bhatia, K.P. (2006). The entity of young onset primary cervical dystonia.
Schneider, S.A., Bhatia, K.P. (2006). The sodium amytal and benzodiazepine interview and its possible application in psychogenic movement disorders. In Hallett, M., Fahn, S., Jankovic, J., Lang, A.E., Cloninger, R.C., Yudofsky, S.C. (Eds.), Psychogenic Movement Disorders: neurology and neuropsychiatry. (pp. 249-255). Philadelphia: Lippincott, Williams & Wilkins.
van de Warrenburg, B.P., Giunti, P., Schneider, S.A., Quinn, N.P., Wood, N.W., Bhatia, K.P. (2006). The syndrome of (predominantly cervical) dystonia and cerebellar ataxia: new cases indicate a distinct but heterogeneous entity.
Healy, D.G., Abou-Sleiman, P.M., Casas, J.P., Ahmadi, K.R., Lynch, T., Gandhi, S., ...Bhatia, K.P. (2006). UCHL-1 is not a Parkinson's disease susceptibility gene. 59 627-633.

2005

Anderson, K.N., Bhatia, K.P., Losseff, N.A. (2005). A case of restless legs syndrome in association with stroke. Sleep, 28 (1), 147-148.
Gilks, W.P., Abou-Sleiman, P.M., Gandhi, S., Jain, S., Singleton, A., Lees, A.J., ...Quinn, N.P. (2005). A common LRRK2 mutation in idiopathic Parkinson's disease.. The Lancet, 365 (9457), 415-416. doi:10.1016/S0140-6736(05)17830-1
Mir, P., Huang, Y.Z., Gilio, F., Edwards, M.J., Berardelli, A., Rothwell, J.C., Bhatia, K.P. (2005). Abnormal cortical and spinal inhibition in paroxysmal kinesigenic dyskinesia. Brain, 128 (2), 291-299. doi:10.1093/brain/awh342
Mir, P., Edwards, M.J., Curtis, A.R.J., Bhatia, K.P., Quinn, N.P. (2005). Adult-onset generalized dystonia due to a mutation in the neuroferritinopathy gene. Movement Disorders, 20 (2), 243-245.
Schneider, S.A., Edwards, M.J., Quinn, N.P., Bhatia, K.P. (2005). Adult-onset primary lower limb dystonia: Clinical description of a rare entity.
Tisch, S., Limousin, P., Quinn, N., Bhatia, K., Hariz, M. (2005). Clinical improvement following bilateral globus pallidus interna deep brain stimulation for generalised dystonia.
Katzenschlager, R., Hughes, A., Evans, A., Manson, A.J., Hoffman, M., Swinn, L., ...Lees, A.J. (2005). Continuous subcutaneous apomorphine therapy improves Dyskinesias in Parkinson's disease: A prospective study using single-dose challenges. Movement Disorders, 20 (2), 151-157.
Bhatia, K.P., Lang, A.E. (2005). Corticobasal degeneration. In Neurodegenerative Diseases: Neurobiology, Pathogenesis and Therapeutics. (pp. 682-696). .
Khan, N.L., Scherfler, C., Graham, E., Bhatia, K.P., Quinn, N., Lees, A.J., ...Piccini, P. (2005). Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation. Neurology, 64 (1), 134-136.
Kim, H.T., Edwards, M.J., Lakshmi Narsimhan, R., Bhatia, K.P. (2005). Hyperthyroidism exaggerating parkinsonian tremor: A clinical lesson. Parkinsonism and Related Disorders, 11 (5), 331-332. doi:10.1016/j.parkreldis.2005.01.009
Graves, T., Imbrici, P., Eunson, L., Bhatia, K.P., Wodia, N.H., Hanna, M.G., Kullmann, D.M. (2005). Late onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A.
Imbrici, P., Eunson, L.H., Graves, T.D., Bhatia, K.P., Wadia, N.H., Kullmann, D.M., Hanna, M.G. (2005). Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A. Neurology, 65 (6), 944-946.
Warner, T.T., Cano, S.J., Edwards, M., FitzPatrick, R., Thompson, A.J., Bhatia, K.P. (2005). Measuring clinical change in cervical dystonia: A comparison of the CDIP-58 with existing rating scales.
Edwards, M.J., Huang, K.Z., Mir, P., Trender-Gerhard, I., Rothwell, J.C., Bhatia, K.P. (2005). Motor system inhibition in dopa-responsive dystonia and its modulation by levodopa treatment.
Huang, Y.Z., Trender-Gerhard, L., Edwards, M.J., Mir, P., Rothwell, J.C., Bhatia, K.P. (2005). Motor system inhibition in dopa-responsive dystonia and its modulation by treatment.
Khan, N.L., Jain, S., Lynch, J.M., Pavese, N., Abou-Sleiman, P., Holton, J.L., ...Ganguly, M. (2005). Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. Brain, 128 (12), 2786-2796.
Tinazzi, M., Gerschlager, W., Bhatia, K.P. (2005). Orthostatic tremor. In Lyons, K.E., Pahwa, R. (Eds.), Handbook of Essential Tremor and Other Tremor Disorders. (pp. 251-261). Boca Raton: Taylor & Francis.
Kuoppamaki, M., Rothwell, J.C., Brown, R.G., Quinn, N., Bhatia, K.P., Jahanshahi, M. (2005). Parkinsonism following bilateral lesions of the globus pallidus: performance on a variety of motor tasks shows similarities with Parkinson's disease. Journal of Neurology, Neurosurgery and Psychiatry, 76 (4), 482-490.
Schneider, S.A., Quinn, N.P., Surtees, R., Bhatia, K.P. (2005). Paroxysmal dyskinesias and seizures associated with hemiplegic migraine: A report of three cases.
Bhatia, K.P. (2005). Paroxysmal dyskinesias in humans. In Movement Disorders. (pp. 449-457). .
Munchau, A., Bhatia, K.P., Schneider, S.A. (2005). Pharmacological treatment of Parkinson's disease. In Morris, H. (Ed.), Neurology update: reviews for continuing professional development. (pp. 197-213). Oxford: Radcliffe Publishing.
Bhatt, M.H., Chhaya, N.A., Vaidya, S.R., Quinn, N., Bhatia, K.P. (2005). Prevalence of Parkinson's disease in the Parsee (Zoroastrian) community.
Kim, H.T., Shields, S., Bhatia, K.P., Quinn, N. (2005). Progressive supranuclear palsy-like phenotype associated with bilateral hypoxic-ischemic striopallidal lesions. Movement Disorders, 20 (6), 755-757.
Mahapatra, R.K., Mir, P., Edwards, M.J., Allen, D., Bhatia, K.P. (2005). Secondary generalized dystonia without basal ganglia damage. Parkinsonism and Related Disorders, 11 (2), 121-123.
Tinazzi, M., Stanzani, C., Fiorio, M., Smania, N., Moretto, G., Fiaschi, A., ...Rothwell, J.C. (2005). Temporal discrimination of two passive movements in humans: a new psychophysical approach to assessing kinaesthesia. Experimental Brain Research, 166 (2), 184-189.
Tinazzi, M., Farina, S., Bhatia, K., Fiaschi, A., Moretto, G., Bertolasi, L., ...Smania, N. (2005). TENS for the treatment of writer's cramp dystonia: A randomized, placebo-controlled study. NEUROLOGY, 64 (11), 1946-1948. doi:10.1212/01.WNL.0000163851.70927.7E
Valente, E.M., Edwards, M.J., Mir, P., DiGiorgio, A., Salvi, S., Davis, M., ...Pennisi, G. (2005). The epsilon-sarcoglycan gene in myoclonic syndromes. Neurology, 64 (4), 737-739.
Edwards, M.J., Hooker, J., Mir, P., Quinn, N.P., Bhatia, K.P. (2005). The usefulness of SPECT DAT scans in differentiating dystonic rest tremor from Parkinson's disease: Some illustrative cases.
Huang, Y.Z., Edwards, M.J., Rounis, E., Bhatia, K.P., Rothwell, J.C. (2005). Theta burst stimulation of the human motor cortex. Neuron, 45 (2), 201-206. doi:10.1016/j.neuron.2004.12.033
Tisch, S., Limousin, P., Jahanshahi, M., Bhatia, K.P., Quinn, N., Hariz, M. (2005). Time-course, predictors, and regional distribution of improvement in primary generalised dystonia following pallidal deep brain stimulation.
Martino, D., Tanner, A., Defazio, G., Church, A.J., Bhatia, K.P., Giovannoni, G., Dale, R.C. (2005). Tracing Sydenham's chorea: historical documents from a British paediatric hospital. Archives of Disease in Childhood, 90 (5), 507-511.
Papapetropoulos, S., Scaravilli, T., Morris, H., An, S.F., Henderson, D.C., Quinn, N.P., ...Bhatia, K.P. (2005). Young onset limb spasticity with PSP-like brain and spinal cord NFT-tau pathology. Neurology, 64 (4), 731-733.

2004

Edwards, M.J., Dale, R.C., Church, A.J., Giovannoni, G., Bhatia, K.P. (2004). A dystonic syndrome associated with anti-basal ganglia antibodies. Journal of Neurology, Neurosurgery and Psychiatry, 75 (6), 914-916.
Healy, D.G., Abou-Sleiman, P.M., Ozawa, T., Lees, A.J., Bhatia, K., Ahmadi, K.R., ...Kamm, C. (2004). A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease. Annals of Neurology, 55 (3), 443-446. doi:10.1002/ana.20063
Healy, D.G., Abou-Sleiman, P.M., Ozawa, T., Lees, A.J., Bhatia, K., Ahmai, K.R., ...Kamm, C. (2004). A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease.(vol 55, 443, 2004). ANNALS OF NEUROLOGY, 56 (2), 311. doi:10.1002/ana.20235
Scaravilli, T., Papapetropoulos, S., Morris, H., Quinn, N.P., Scaravilli, F., Bhatia, K.P. (2004). A patient with PSP-like brain and spinal cord NFT-tau pathology presenting as young onset spastic paraplegia.
Bhatt, M., Sethi, K.D., Bhatia, K. (2004). Acute and tardive dystonia. In Sethi, K.D. (Ed.), Drug-induced movement disorders. (pp. 111-128). New York: Marcel Dekker, Inc..
Edwards, M.J., Dale, R.C., Church, A.J., Trikouli, E., Quinn, N.P., Lees, A.J., ...Bhatia, K.P. (2004). Adult-onset tic disorder, motor stereotypies, and behavioural disturbance associated with antibasal ganglia antibodies. Movement Disorders, 19 (10), 1190-1196.
Edwards, M.J., Trikouli, E., Martino, D., Church, A.J., Giovannoni, G., Bhatia, K.P. (2004). Antibasal ganglia antibodies in atypical dystonia and tics: A prospective study.
Edwards, M.J., Trikouli, E., Martino, D., Bozi, M., Dale, R.C., Church, A.J., ...Giovannoni, G. (2004). Anti-basal ganglia antibodies in patients with atypical dystonia and tics - A prospective study. Neurology, 63 (1), 156-158.
Edwards, M.J., Trikouli, E., Martino, D., Bozi, M., Dake, R.C., Church, A.J., ...Giovannoni, G. (2004). Anti-basal ganglia antibodies in patients with atypical dystonia and tics: A prospective study.
Sinha, K.K., Worth, P.F., Jha, D.K., Sinha, S., Stinton, V.J., Davis, M.B., ...Bhatia, K.P. (2004). Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India. Journal of Neurology, Neurosurgery and Psychiatry, 75 (3), 448-452.
Khan, N.L., Bhatt, M., Khan, N., Brooks, D.J., Piccini, P., Bhatia, K.P. (2004). Autosomal dominant, neuroleptic-induced reversible, dystonia and parkinsonism.
Tisch, S., Limousin, P., Rothwell, J., Asselmann, P., Bhatia, K., Hariz, M. (2004). Blink reflex R2 inhibition following pallidal deep brain stimulation for dystonia.
Cano, S.J., Warner, T.T., Linacre, J.M., Bhatia, K.P., Thompson, A.J., Fitzpatrick, R., Hobart, J.C. (2004). Capturing the true burden of dystonia on patients: the Cervical Dystonia Impact Profile (CDIP-58). Neurology, 63 (9), 1629-1633.
Pereira, A.C., Edwards, M.J., Buttery, P.C., Hawkes, C.H., Quinn, N.P., Giovannoni, G., ...Bhatia, K.P. (2004). Choreic syndrome and coeliac disease: A hitherto unrecognised association. Movement Disorders, 19 (4), 478-482.
Filipovic, S.R., Jahanshahi, M., Viswanathan, R., Heywood, P., Rogers, D., Bhatia, K.P. (2004). Clinical features of the geste antagoniste in cervical dystonia. Advances in Neurology, 94 (4), 191-201.
Mahapatra, R.K., Bozi, M., Mir, P., Chuang, C., Edwards, M., Bhatia, K.P. (2004). Clinical heterogeneity in vascular parkinsonism.
Martino, D., Chew, N.K., Mir, P., Cifelli, A., Bajaj, N., Edwards, M.J., Bhatia, K.P. (2004). Clinical heterogeneity of movement disorders associated with antiphospholipid syndrome.
Chew, N.K., Martino, D., Mir, P., Bajaj, N., Edwards, M., Bhatia, K.P. (2004). Clinical heterogeneity of movement disorders associated with antiphospholipid syndrome.
Lucas, V.S., Roberts, G.J. (2004). Commentary.
Mahapatra, R.K., Edwards, M.J., Schott, J.M., Bhatia, K.P. (2004). Corticobasal degeneration. The Lancet Neurology, 3 (12), 736-743.
Cano, S.J., Hobart, J.C., Thompson, A.J., Bhatia, K., Fitzpatrick, R., Warner, T.T. (2004). Develepment and validation of a new dystonia patient-based outcome measure: The Cervical Dystonia Impact Profile (CDIP-58).
Edwards, M.J., Huang, Y.Z., Rothwell, J.C., Bhatia, K.P. (2004). Different patterns of electrophysiological deficit in manifesting and non-manifesting carriers of the DYT1 gene.
Edwards, M.J., Huang, Y.Z., Mir, P., Rothwell, J.C., Bhatia, K.P. (2004). Differential motor system plasticity in manifesting and non manifesting DYT1 gene carriers.
Edwards, M.J., Huang, Y.Z., Mir, P., Rothwell, J.C., Bhatia, K.P. (2004). Differential motor system plasticity is linked to development of dystonia in DYT1 mutation carriers. EUROPEAN JOURNAL OF NEUROLOGY, 11 353.
Healy, D.G., Abou-Sleiman, P.M., Valente, E.M., Gilks, W.P., Bhatia, K., Quinn, N., ...Wood, N.W. (2004). DJ-1 mutations in Parkinson's disease. Journal of Neurology, Neurosurgery and Psychiatry, 75 (1), 144-145.
Healy, D.G., Abou-Sleiman, P.M., Ozawa, T., Lees, A.J., Bhatia, K., Ahmai, K.R., ...Kamm, C. (2004). Erratum: A functional polymorphism regulating dopamine β-hydroxylase influences against Parkinson's disease (Annals of Neurology (March 2004) 55 (443-446) DOI: 10.1002/ana.20235. Annals of Neurology, 56 (2), 311-.
Bloem, B.R., Bhatia, K.P. (2004). Gait and balance in basal ganglia disorders. In Bronstein, A., Brandt, T., Woollacott, M.H., Nutt, J.G. (Eds.), Clinical Disorders of Balance, Posture and Gait. (pp. 173-206). London: Arnold.
Russo, N., Edwards, M., Andrews, T., O'Brien, M., Bhatia, K.P. (2004). Hereditary haemochromatosis is unlikely to cause movement disordersA critical review. Journal of Neurology, 251 (7), 849-852.
Gerhard, A., Watts, J., Trender-Gerhard, I., Turkheimer, F., Banati, R.B., Bhatia, K., Brooks, D.J. (2004). In vivo imaging of microglial activation with [C-11](R)-PK 11195 PET in corticobasal degeneration. Movement Disorders, 19 (10), 1221-1226.
Filipovic, S.R., Siebner, H.R., Rowe, J.B., Cordivari, C., Gerschlager, W., Rothwell, J.C., ...Bhatia, K.P. (2004). Modulation of cortical activity by repetitive transcranial magnetic stimulation (rTMS): a review of functional imaging studies and the potential use in dystonia. Advances in Neurology, 94 (1), 45-52.
Gerschlager, W., Munchau, A., Katzenschlager, R., Brown, P., Rothwell, J.C., Quinn, N., ...Bhatia, K.P. (2004). Natural history and syndromic associations of orthostatic tremor: A review of 41 patients. Movement Disorders, 19 (7), 788-795.
Schrag, A., Bhatt, M., Soonawala, N., Quinn, N.P., Bhatia, K.P. (2004). Occurrence of atypical parkinsonism in Indians and Caucasians. Acta Neurologica Scandinavica, 109 (2), 155-156.
Khan, N.L., Katzenschlager, R., Watt, H., Bhatia, K.P., Wood, N.W., Quinn, N., Lees, A.J. (2004). Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease.. Neurology, 62 (7), 1224-1226.
Huang, Y.Z., Edwards, M.J., Bhatia, K.P., Rothwell, J.C. (2004). One-Hz repetitive transcranial magnetic stimulation of the premotor cortex alters reciprocal inhibition in DYT1 dystonia. Movement Disorders, 19 (1), 54-59.
Whone, A.L., Von Spiczak, S., Edwards, M., Valente, E.M., Hammers, A., Bhatia, K.P., Brooks, D.J. (2004). Opioid binding in DYT1 primary torsion dystonia: An C-11- diprenorphine PET Study. Movement Disorders, 19 (12), 1498-1503.
Bhatia, K.P. (2004). Paroxysmal Dyskinesias in Humans. In Movement Disorders: Genetics and Models: Second Edition. (pp. 449-457). .
Cano, S.J., Hobart, J.C., Fitzpatrick, R., Bhatia, K., Thompson, A.J., Warner, T.T. (2004). Patient-based outcomes of cervical dystonia: A review of rating scales. Movement Disorders, 19 (9), 1054-1059.
Grosse, P., Edwards, M., Tijssen, M.A.J., Schrag, A., Lees, A.J., Bhatia, K.P., Brown, P. (2004). Patterns of EMG-EMG coherence in limb dystonia. Movement Disorders, 19 (7), 758-769.
Filipovic, S.R., Jahanshahi, M., Viswanathan, R., Heywood, P., Rogers, D., Bhatia, K.P. (2004). Presence of head tremor reduces the effectiveness of the botulimun toxin injections for cervical dystonia: A patients' perspective.
Tarsy, D., Schrag, A., Quinn, N., Bhatia, K. (2004). Psychogenic facial spasm ("The Smirk").
Morgan, J.C., Mir, P., Mahapatra, R.K., Bhatia, K.P., Sethi, K.D. (2004). Psychogenic parkinsonism: Clinical features of a large case series.
Quinn, N.P., Bhatia, K. (2004). Re: Yianni et al., Globus pallidus internus deep brain stimulation for dystonic conditions: a prospective audit. Movement Disorders, 19 (1), 114.
Filipovic, S.R., Heywood, P., Rothwell, J.C., Bhatia, K.P. (2004). Repetitive transcranial magnetic stimulation (rTMS) for levodopa-induced dyskinesias in Parkinson's disease: Preliminary results.
Healy, D.G., Abou-Sleiman, P.M., Lees, A.J., Casas, J.P., Quinn, N., Bhatia, K., ...Wood, N.W. (2004). Tau gene and Parkinson's disease: a case-control study and meta-analysis. 75 962-965.
Cano, S.J., Warner, T.T., Fitzpatrick, R., Bhatia, K., Thompson, A.J., Hobart, J.C. (2004). The cervical dystonia impact profile (CDIP-58): A new patient-based rating scale.
Healy, D.G., Abou-Sleiman, P.M., Ahmadi, K.R., Muqit, M.M.K., Bhatia, K.P., Quinn, N.P., ...Wood, N.W. (2004). The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of Parkinsonism. Annals of Neurology, 56 (3), 329-335. doi:10.1002/ana.20206
Schrag, A., Trimble, M., Quinn, N., Bhatia, K. (2004). The syndrome of fixed dystonia: an evaluation of 103 patients.. Brain, 127 (10), 2360-2372. doi:10.1093/brain/awh262
Schrag, A.E., Trimble, M.R., Quinn, N.P., Bhatia, K. (2004). The syndrome of fixed dystonia: An evaluation of 105 patients.
Huang, Y.Z., Edwards, M.J., Runis, E., Bhatia, K.P., Rothwell, J.C. (2004). Theta burst conditioning of the human cortex with rTMS.
Ben Shlomo, Y., Bhatia, K. (2004). Using monoamine oxidase type B inhibitors in Parkinson's disease - They are effective and safe, at least when used alone. BMJ (Clinical Research Ed.), 329 (7466), 581-582.

2003

Katzenschlager, R., Costa, D., Gerschlager, W., O'Sullivan, J., Zijlmans, J., Gacinovic, S., ...Lees, A.J. (2003). [I-123]-FP-CIT-SPECT demonstrates dopaminergic deficit in orthostatic tremor. Annals of Neurology, 53 (4), 489-496.
Edwards, M., Russo, N., Summers, B., Morton, J., Peake, D., Bhatia, K. (2003). An unusual family with multiple movement disorders. Journal of Neurology, 250 (7), 793-796.
Edwards, M., Russo, N., Summers, B., Morton, J., Peake, D., Bhatia, K. (2003). An unusual family with multiple movement disorders.. JOURNAL OF NEUROLOGY, 250 (7), 793-796. doi:10.1007/s00415-003-1078-0
Khan, N.L., Wood, N.W., Bhatia, K.P. (2003). Autosomal recessive, DYT2-like primary torsion dystonia: a new family. Neurology, 61 (12), 1801-1803.
Edwards, M.J., Huang, Y.Z., Wood, N.W., Rothwell, J.C., Bhatia, K.P. (2003). Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation. Brain, 126 (9), 2074-2080. doi:10.1093/brain/awg209
Edwards, M., Schott, G., Bhatia, K. (2003). Episodic focal lingual dystonic spasms. Movement Disorders, 18 (7), 836-837.
Edwards, M., Schott, G., Bhatia, K. (2003). Episodic focal lingual dystonic spasms.. MOVEMENT DISORDERS, 18 (7), 836-837. doi:10.1002/mds.10436
Katzenschlager, R., Costa, D., Gerschlager, W., O'Sullivan, J., Zijlmans, J., Gacinovic, S., ...Lees, A.J. (2003). Erratum: [¹²I]-FP-CIT-SPECT demonstrates dopaminergic deficit in orthostatic tremor (Annals of Neurology (2003) 53 (489-496)). Annals of Neurology, 54 (2), 278-. doi:10.1002/ana.10704
Cordivari, C., Vincent, A., Misra, V.P., Catania, S., Murray, N.M.F., Bhatia, K.P., Lees, A.J. (2003). Failure to identify change in the cervical dystonia muscle pattern is the main cause of reduced response to BTXA.
Litvan, I., Bhatia, K.P., Burn, D.J., Goetz, C.G., Lang, A.E., McKeith, I., ...Wenning, G.K. (2003). Movement Disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for Parkinsonian disorders. Movement Disorders, 18 (5), 467-486.
Khan, N.L., Graham, E., Critchley, P., Schrag, A.E., Wood, N.W., Lees, A.J., ...Quinn, N. (2003). Parkin disease: a phenotypic study of a large case series. Brain, 126 (6), 1279-1292. doi:10.1093/brain/awg142
Bozi, M., Bhatia, K.P. (2003). Paroxysmal exercise-induced dystonia as a presenting feature of young-onset Parkinson's disease. Movement Disorders, 18 (12), 1545-1547.
Siebner, H.R., Filipovic, S.R., Rowe, J.B., Cordivari, C., Gerschlager, W., Rothwell, J.C., ...Bhatia, K.P. (2003). Patients with focal arm dystonia have increased sensitivity to slow-frequency repetitive TMS of the dorsal premotor cortex. Brain, 126 (12), 2710-2725. doi:10.1093/brain/awg282
Rothwell, J.C., Edwards, M., Huang, Y.Z., Bhatia, K.P. (2003). Physiological studies in carriers of the DYT1 gene mutation. Revue Neurologique, 159 (10), 880-884.
Rothwell, J.C., Edwards, M., Huang, Y.Z., Bhatia, K.P. (2003). Physiological studies in carriers of the DYT1 gene mutation. Revue Neurologique, 159 (10 I), 880-884.
Gerschlager, W., Katzenschlager, R., Schrag, A., Lees, A.J., Brown, P., Quinn, N., Bhatia, K.P. (2003). Quality of life in patients with orthostatic tremor. Journal of Neurology, 250 (2), 212-215.
Sibbing, D., Trender-Gerhardt, I., Wood, N.W., Oertel, W.H., Bhatia, K.P., Bandmann, O. (2003). The promoter region of the Menkes gene ATP7A is not altered in focal or generalized dystonia. Annals of Neurology, 53 (2), 278-279.
Sibbing, D., Trender-Gerhardt, I., Wood, N.W., Oertel, W.H., Bhatia, K.P., Bandmann, O., ...Becker, G. (2003). The promoter region of the menkes gene ATP7A is not altered in focal or generalized dystonia [2] (multiple letters). Annals of Neurology, 53 (2), 278-279. doi:10.1002/ana.10436
Edwards, M., Wood, N., Bhatia, K. (2003). Unusual phenotypes in DYT1 dystonia: A report of five cases and a review of the literature. Movement Disorders, 18 (6), 706-711.
Edwards, M., Wood, N., Bhatia, K. (2003). Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature.. MOVEMENT DISORDERS, 18 (6), 706-711. doi:10.1002/mds.10411

2002

Misbahuddin, A., Placzek, M.R., Chaudhuri, K.R., Wood, N.W., Bhatia, K.P., Warner, T.T. (2002). A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm. Neurology, 58 (1), 124-126.
Russo, N.M., Edwards, M.J., Summers, B.A., Morton, J.E., Peake, D., Bhatia, K.P. (2002). A remarkable association of generalized dystonia, Huntington's disease, progressive supranuclear palsy, and secondary paroxysmal dyskinesia in one family.
Ramachandran, V., Church, A., Giovannoni, G., Bhatia, K.P. (2002). Anti-basal ganglia antibodies are absent in patients with primary blepharospasm. Neurology, 58 (1), 150.
Dressler, D., Munchau, A., Bhatia, K.P., Quinn, N.P., Bigalke, H. (2002). Antibody-induced botulinum toxin therapy failure: can it be overcome by increased botulinum toxin doses?. European Neurology, 47 (2), 118-121.
Khan, N.L., Wood, N.W., Bhatia, K.P. (2002). Autosomal recessive, DYT-2-like primary torsion dystonia: A new family.
Filipovic, S.R., Jahanshahi, M., Viswanathan, R., Heywood, P., Bhatia, K.P. (2002). Clinical features of the geste antagoniste in cervical dystonia. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 73 (2), 215.
Tijssen, M.A.J., Munchau, A., Marsden, J.F., Lees, A., Bhatia, K.P., Brown, P. (2002). Descending control of muscles in patients with cervical dystonia. Movement Disorders, 17 (3), 493-500.
Edwards, M.J., Dale, R.C., Church, A.J., Giovannoni, G., Bhatia, K.P. (2002). Dystonia in adolescents and adults associated with anti-basal ganglia antibodies.
Guerrini, R., Sanchez-Carpintero, R., Deonna, T., Santucci, M., Bhatia, K.P., Moreno, T., ...Bernardina, B.D. (2002). Early-onset absence epilepsy and paroxysmal dyskinesia. Epilepsia, 43 (10), 1224-1229.
Bajaj, N.P.S., Waldman, A., Orrell, R., Wood, N.W., Bhatia, K.P. (2002). Familial adult onset of Krabbe's disease resembling hereditary spastic paraplegia with normal neuroimaging. Journal of Neurology, Neurosurgery and Psychiatry, 72 (5), 635-638.
Barnett, M.H., Jarman, P.R., Heales, S.J.R., Bhatia, K.P. (2002). Further case of paroxysmal exercise-induced dystonia and some insights into pathogenesis. Movement Disorders, 17 (6), 1386-1387.
Spacey, S.D., Valente, E.M., Wali, G.M., Warner, T.T., Jarman, P.R., Schapira, A.H.V., ...Wood, N.W. (2002). Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene. Movement Disorders, 17 (4), 717-725.
Munchau, A., Orth, M., Rothwell, J.C., Di Lazzaro, V., Oliviero, A., Profice, P., ...Bhatia, K.P. (2002). Intracortical inhibition is reduced in a patient with a lesion in the posterolateral thalamus. Movement Disorders, 17 (1), 208-212.
Asmus, F., Zimprich, A., Tezenas Du, M.S., Kabus, C., Deuschl, G., Kupsch, A., ...Strom, T.M. (2002). Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype. Annals of Neurology, 52 (4), 489-492.
Edwards, M.J.J., Hargreaves, I.P., Heales, S.J.R., Jones, S.J., Ramachandran, V., Bhatia, K.P., Sisodiya, S. (2002). N-acetylcysteine and Unverricht-Lundborg disease - Variable response and possible side effects. Neurology, 59 (9), 1447-1449.
Eunson, L., Khan, N.L., Quinn, N., Bhatia, K., Wood, N.W., Davis, M.B. (2002). Novel parkin mutations in early-onset parkinsonism.
Bhatia, K.P. (2002). Other extrapyramidal syndromes: parkinsonism-plus and other forms of secondary parkinsonism. In Asbury, A.K., McKhann, G.M., McDonald, W.I., Goadsby, P.J., McArthur, J.C. (Eds.), Diseases of the nervous system: clinical neuroscience and therapeutic principles. (pp. 490-512). Cambridge: Cambridge University Press.
Bhatia, K.P. (2002). Other extrapyramidal syndromes:parkinsonism-plus and other forms of secondary parkinsonism. In Diseases of the Nervous System Clinical Neuroscience and Therapeutic Principles. (pp. 489-511). Cambridge University Press.
Bozi, M., Bhatia, K.P. (2002). Paroxysmal exercise-induced dystonia as the initial manifestation of Parkinson's disease.
Cordivari, C., Vincent, A., Misra, V.P., Catania, S., Bhatia, K.P., Lees, A.J. (2002). Patients with cervical dystonia thought to be secondary non responders to botulinum toxin treatment should be given a trial of EMG guided injections.
Kuoppamaki, M., Bhatia, K.P., Quinn, N. (2002). Progressive delayed-onset dystonia after cerebral anoxic insult in adults. Movement Disorders, 17 (6), 1345-1349.
Obeso, J.A., Bhatia, K., Rothwell, J.C. (2002). The contribution of C. David Marsden to the study and treatment of myoclonus. MYOCLONUS AND PAROXYSMAL DYSKINESIAS, 89 1-12.
Khan, N., Valente, E.M., Brooks, D.J., Piccini, P., Bhatia, K.P., Quinn, N.P., Wood, N.W. (2002). The genetic basis and phenotypic variability in early onset parkinsonism. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 73 (2), 213.
Quinn, N., Bhatia, K. (2002). The man who walks backwards. Journal of the Royal Society of Medicine, 95 (5), 273.
Edwards, M.J., Hargreaves, I.P., Heales, S.J., Jones, S.J., Ramachandran, V., Bhatia, K.P. (2002). The treatment of Unverricht-Lundborg disease with N-acetylcysteine.
Edwards, M.J., Wood, N.W., Bhatia, K.P. (2002). Unusual phenotypes in DYT1 dystonia: A report of 5 cases and review of the literature.

2001

Bajaj, N.P.S., Waldman, A.D., Orrell, R.W., Bhatia, K.P. (2001). A unique family with adult onset Krabbe disease and normal neuroimaging.
Munchau, A., Corna, S., Gresty, M.A., Bhatia, K.P., Palmer, J.D., Dressler, D., ...Bronstein, A.M. (2001). Abnormal interaction between vestibular and voluntary head control in patients with spasmodic torticollis. Brain, 124 (1), 47-59.
Munchau, A., Schrag, A., Chuang, C., MacKinnon, C.D., Bhatia, K.P., Quinn, N.P., Rothwell, J.C. (2001). Arm tremor in cervical dystonia differs from essential tremor and can be classified by onset age and spread symptoms. Brain, 124 (9), 1765-1776. doi:10.1093/brain/124.9.1765
Placzek, M.R., Misbahuddin, A., Chaudhuri, K.R., Wood, N.W., Bhatia, K.P., Warner, T.T. (2001). Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene. Journal of Neurology, Neurosurgery and Psychiatry, 71 (2), 262-264.
Houlden, H., Baker, M., Morris, H.R., MacDonald, N., Pickering-Brown, S., Adamson, J., ...Kertesz, A. (2001). Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype. Neurology, 56 (12), 1702-1706.
Bhatia, K.P. (2001). Familial (idiopathic) paroxysmal dyskinesias: an update. Seminars in Neurology, 21 (1), 69-74.
Bhatia, K.P. (2001). Familial (idiopathic) paroxysmal dyskinesias: An update. Seminars in Neurology, 21 (1), 69-74. doi:10.1055/s-2001-13121
Bajaj, N.P.S., Waldman, A.D., Quinn, N.P., Palace, J., Ron, M., Bhatia, K.P. (2001). Hallervorden-Spatz syndrome: unusual presentation and MRS study. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 70 (2), 275.
Dickson, D.W., Anderton, B., Morris, H., Hodges, J., Bak, T.H., Dubois, B., ...Golbe, L.I. (2001). International medical workshop covering progressive supranuclear palsy, Multiple System Atrophy and cortico basal degeneration. Movement disorders : official journal of the Movement Disorder Society, 16 (2), 382-395. doi:10.1002/mds.1074
Bhatia, K.P., Valente, E.M. (2001). Paroxysmal movement disorders as channelopathies. In Rose, M., Griggs, R.C. (Eds.), Channelopathies of the nervous system. (pp. 250-258). Oxford: Butterworth Heinemann.
Munchau, A., Bahlke, G., Allen, P.J., Quinn, N.P., Lees, A.J., Rothwell, J.C., ...Bhatia, K.P. (2001). Polymyography combined with time-locked video recording (video EMG) for presurgical assessment of patients with cervical dystonia. European Neurology, 45 (4), 222-228.
Munchau, A., Palmer, J.D., Dressler, D., O'Sullivan, J.D., Tsang, K.L., Jahanshahi, M., ...Bhatia, K.P. (2001). Prospective study of selective peripheral denervation for botulinum-toxin resistant patients with cervical dystonia. Brain, 124 (4), 769-783.
Munchau, A., Good, C.D., McGowan, S., Quinn, N.P., Palmer, J.D., Bhatia, K.P. (2001). Prospective study of swallowing function in patients with cervical dystonia undergoing selective peripheral denervation. Journal of Neurology, Neurosurgery and Psychiatry, 71 (1), 67-72.
Bhatia, K.P. (2001). Psychogenic gait disorders. In Ruzicka, E., Hallett, M., Jankovic, J. (Eds.), Gait disorders. (pp. 251-254). London: Lippincott, Williams and Wilkins.
Munchau, A., Filipovic, S.R., Oester-Barkey, A., Quinn, N.P., Rothwell, J.C., Bhatia, K.P. (2001). Spontaneously changing muscular activation pattern in patients with cervical dystonia. Movement Disorders, 16 (6), 1091-1097.
Bhatia, K.P., Brooks, D.J., Burn, D.J., Clarke, C.E., Grosset, D.G., MacMahon, D.G., ...Williams, A.C. (2001). Updated guidelines for the management of Parkinson's disease. Hospital Medicine, 62 (8), 456-470.

2000

Munchau, A., Valente, E.M., Shahidi, G.A., Eunson, L.H., Hanna, M.G., Quinn, N.P., ...Bhatia, K.P. (2000). A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 68 (5), 609-614.
Valente, E.M., Spacey, S.D., Wali, G.M., Bhatia, K.P., Dixon, P.H., Wood, N.W., Davis, M.B. (2000). A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16. Brain, 123 2040-2045.
Munchau, A., Valente, E.M., Davis, M.B., Stinton, V.J., Wood, N.W., Quinn, N.P., Bhatia, K.P. (2000). A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia. Movement Disorders, 15 (5), 954-959.
Schrag, A., Quinn, N.P., Bhatia, K.P., Marsden, C.D. (2000). Benign hereditary chorea: entity or syndrome ?. Movement Disorders, 15 (2), 280-288.
Bhatia, K.P. (2000). Benzodiazepines in the treatment of movement disorders. In Trimble, M.R., Hindmarch, I. (Eds.), Benzodiazepines. (pp. 121-130). Petersfield: Wrightson Biomedical Publishing Ltd.
Dressler, D., Dirnberger, G., Bhatia, K.P., Irmer, A., Quinn, N.P., Bigalke, H., Marsden, C.D. (2000). Bilateral striatal necrosis associated with Mycoplasma pneumoniae infection in an adolescent: Clinical and neuroradiologic follow up. Movement Disorders, 15 (5), 1023-1026. doi:10.1002/1531-8257(200009)15:5<1023::AID-MDS1045>3.0.CO;2-A
O'Sullivan, J.D., Bhatia, K.P., Lees, A.J. (2000). Botulinum toxin A as treatment for drooling saliva in PD. Neurology, 55 (4), 606-607.
O'Sullivan, J.D., Bhatia, K.P., Lees, A.J. (2000). Botulinum toxin A as treatment for drooling saliva in PD [7] (multiple letters). Neurology, 55 (4), 606-607. doi:10.1212/WNL.55.4.606-a
Dressler, D., Dirnberger, G., Bhatia, K.P., Irmler, A., Quinn, N.P., Bigalke, H., Marsden, C.D. (2000). Botulinum toxin antibody testing: comparison between the mouse protection assay and the mouse lethality assay. Movement Disorders, 15 (5), 973-976.
Bhatia, K.P., Lee, M.S., Rinne, J.O., Revesz, T., Scaravilli, F., Davies, L., Marsden, C.D. (2000). Corticobasal degeneration look-alikes. In Litvan, I., Goetz, C.G., Lang, A.E. (Eds.), Corticobasal degeneration and related disorders. (pp. 169-182). New York: Lippincott-Raven.
Bhatia, K.P., Griggs, R.C., Ptacek, L.J. (2000). Episodic movement disorders as channelopathies. Movement Disorders, 15 (3), 429-433.
Bhatia, K.P., Griggs, R.C., Ptek, L.J. (2000). Episodic movement disorders as channelopathies. Movement Disorders, 15 (3), 429-433. doi:10.1002/1531-8257(200005)15:3<429::AID-MDS1001>3.0.CO;2-R
Bhatia, K.P., Griggs, R.C., Ptáček, L.J. (2000). Episodic movement disorders as channelopathies.. Movement disorders : official journal of the Movement Disorder Society, 15 (3), 429-433. doi:10.1002/1531-8257(200005)15:3<429::aid-mds1001>3.0.co;2-r
Schrag, A., Munchau, A., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (2000). Essential tremor: an overdiagnosed condition?. Journal of Neurology, 247 (12), 955-959.
Jarman, P.R., Bhatia, K.P., Davie, C., Heales, S.J.R., Turjanski, N., Taylor-Robinson, S.D., ...Wood, N.W. (2000). Paroxysmal dystonic choreoathetosis: Clinical features and investigation of pathophysiology in a large family. Movement Disorders, 15 (4), 648-657. doi:10.1002/1531-8257(200007)15:4<648::AID-MDS1008>3.0.CO;2-T
Jarman, P.R., Bhatia, K.P., Davie, C.A., Heales, S.J.R., Turjanski, N., Taylor-Robinson, S.D., ...Wood, N.W. (2000). Paroxysmal dystonic choreoathetosis: clinical features and investigation of pathophysiology in a large family. Movement Disorders, 15 (4), 648-657.
Houlden, H., Baker, M., Bhatia, K., Hutton, M., Wood, N. (2000). Pathologically confirmed corticobasal degeneration shares the same tau haplotype association as progressive supranuclear palsy. ANNALS OF NEUROLOGY, 48 (3), 436.
Chawda, S.J., Munchau, A., Johnson, D.R., Bhatia, K.P., Quinn, N.P., Stevens, J., ...Palmer, J.D. (2000). Pattern of premature degenerative changes of the cervical spine in patients with spasmodic torticollis and the impact on the outcome of selective peripheral denervation. Journal of Neurology, Neurosurgery and Psychiatry, 68 (4), 465-471.
Crimlisk, H.L., Bhatia, K.P., Cope, H., David, A.S., Marsden, C.D., Ron, M.A. (2000). Patterns of referral in patients with medically unexplained motor symptoms. Journal of Psychosomatic Research, 49 217-219.
Munchau, A., Bhatia, K.P. (2000). Pharmacological treatment of Parkinson's disease. Postgraduate Medical Journal, 76 (900), 602-610.
Munchau, A., Bhatia, K.P. (2000). Regular review - Uses of botulinum toxin injection in medicine today. BRITISH MEDICAL JOURNAL, 320 (7228), 161-165. doi:10.1136/bmj.320.7228.161
Hanagasi, H.A., Kaptanoglu, G., Sahin, H.A., Emre, M. (2000). The use of NMDA antagonist memantine in drug-resistant dyskinesias resulting from L-dopa. MOVEMENT DISORDERS, 15 (5), 1016-1017. doi:10.1002/1531-8257(200009)15:5<1016::AID-MDS1042>3.0.CO;2-J
Munchau, A., Mathen, D., Cox, T., Quinn, N.P., Marsden, C.D., Bhatia, K.P. (2000). Unilateral lesions of the globus pallidus: report of four patients presenting with focal or segmental dystonia. Journal of Neurology, Neurosurgery and Psychiatry, 69 (4), 494-498.
Munchau, A., Bhatia, K.P. (2000). Uses of botulinum toxin injection in medicine today. BMJ (Clinical Research Ed.), 320 (7228), 161-165.

1999

Lee, M.S., Kim, Y.D., Im, J.H., Kim, H.J., Rinne, J.O., Bhatia, K.P. (1999). ¹²³I-IPT brain SPECT study in essential tremor and Parkinson's disease. Neurology, 52 (7), 1422-1426. doi:10.1212/wnl.52.7.1422
Lee, M.S., Kim, Y.D., Im, J.H., Kim, H.J., Rinne, J.O., Bhatia, K.P. (1999). 123I-IPT brain SPECT study in essential tremor and Parkinson's disease. Neurology, 52 1422-1426.
Bhatia, K.P., Muenchau, A., Valente, E., Shahidi, G., Quinn, N.P., Wood, N.W. (1999). A new family with paroxysmal exercise-induced dystonia and associated migraine. NEUROLOGY, 52 (6), A119.
Schrag, A., Bhatia, K., Brown, P., Marsden, C.D. (1999). An unusual jaw tremor with characteristics of primary orthostatic tremor. Movement Disorders, 14 (3), 528-530.
Schrag, A., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1999). Atypical and typical cranial dystonia following dental procedures. Movement Disorders, 14 (3), 492-496.
Quinn, N.P., Schrag, A.E., Bhatia, K.P., Marsden, C.D. (1999). Benign hereditary chorea: Entity or syndrome?. NEUROLOGY, 52 (6), A121.
Bhatia, K.P., Munchau, A., Brown, P. (1999). Botulinum toxin is a useful treatment in excessive drooling of saliva. Journal of Neurology, Neurosurgery and Psychiatry, 67 697-.
Bhatia, K.P. (1999). Case 33. In Wills, A.J., Marsden, C.D. (Eds.), Fifty neurological cases from the National Hospital. (pp. 109-110). London: Martin Dunitz.
Kiriakakis, V., Caputo, E., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1999). CLINICAL DIFFERENCES BETWEEN TARDIVE AND IDIOPATHIC CERVICAL DYSTONIA..
Bhatia, K.P., Munchau, A., Thompson, P.D., Houser, M., Chauhan, V.S., Hutchinson, M., ...Marsden, C.D. (1999). Generalised muscular weakness after botulinum toxin injections for dystonia: a report of three cases. Journal of Neurology, Neurosurgery and Psychiatry, 67 90-93.
Soonawala, N., Bhatia, K.P., Yeung, J.H., Quinn, N.P., Marsden, C.D. (1999). Idiopathic blepharospasm does not lead to a parkinsonian syndrome: results of a questionnaire-based follow-up study.. JOURNAL OF NEUROLOGY, 246 (4), 283-286. doi:10.1007/s004150050347
Munchau, A., Dressler, D., Bhatia, K.P., Vogel, P., Zuhlke, C. (1999). Machado-Joseph disease presenting as severe generalised dystonia in a German patient. Journal of Neurology, 246 (9), 840-842.
Schrag, A., Muenchau, A., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1999). Overdiagnosis of essential tremor. The Lancet, 353 (9163), 1498-1499.
Houser, M.K., Soland, V.L., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1999). Paroxysmal kinesigenic choreoathetosis: a report of 26 patients. Journal of Neurology, 246 120-126.
Pramstaller, P.P., Salerno, A., Bhatia, K.P., Prugger, M., Marsden, C.D. (1999). Primary central neurons system lymphoma presenting with a parkinsonian syndrome of pure akinesia. Journal of Neurology, 246 934-938.
Muenchau, A., Palmer, J., Dressler, D., Quinn, N.P., Lees, A., Bhatia, K.P. (1999). Selective peripheral denervation with posterior primary ramisectomy is useful for botulinum toxin resistant patients with cervical dystonia: Results of a prospective study. NEUROLOGY, 52 (6), A294.
Mathen, D., Marsden, C.D., Bhatia, K.P. (1999). SSRI-induced reversal of levodopa benefit in two patients with dopa-responsive dystonia. Movement Disorders, 14 (5), 874-876.
Mathen, D., Marsden, C.D., Bhatia, K.P. (1999). SSRI-induced reversal of levodopa benefit in two patients with dopa-responsive dystonia. Movement Disorders, 14 (5), 874-876. doi:10.1002/1531-8257(199909)14:5<874::AID-MDS1028>3.0.CO;2-Q
Schrag, A., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1999). The dancing larynx - a variant of palatal tremor?. Movement Disorders, 14 (5), 882-883.
Whurr, R., Bhatia, K., Masarei, A., Lorch, M., Kingsley, D., Pramstaller, P., ...Marsden, C.D. (1999). The incidence and nature of dysphagia following botulinum toxin injections for torticollis: A prospective study of 123 patients. JOURNAL OF MEDICAL SPEECH-LANGUAGE PATHOLOGY, 7 (3), 195-207.
Bhatia, K.P. (1999). The paroxysmal dyskinesias. Journal of Neurology, 246 149-155.

1998

Phillips, H.A., Scheffer, I.E., Crossland, K.M., Bhatia, K.P., Fish, D.R., Marsden, C.D., ...Plazzi, G. (1998). Autosomal dominant nocturnal frontal-lobe epilepsy: Genetic heterogeneity and evidence for a second locus at 15q24. The American Journal of Human Genetics, 63 1108-1116.
Kompoliti, K., Goetz, C.G., Boeve, B.F., Maraganore, D.M., Ahlskog, J.E., Marsden, C.D., ...Seal, E.C. (1998). Clinical presentation and pharmacological therapy in corticobasal degeneration. Archives of Neurology, 55 957-961.
Quinn, N., Bhatia, K. (1998). Functional neurosurgery for Parkinson's disease. British Medical Journal, 316 (7140), 1259-1260. doi:10.1136/bmj.316.7140.1259
Quinn, N.P., Bhatia, K.B. (1998). Functional neurosurgery for Parkinson's disease has come a long way, though much remains experimental. BMJ (Clinical Research Ed.), 316 1259-1260.
Bhatia, K.P., Brooks, D.J., Burn, D.J., Clarke, C.E., Playfer, J., Sawle, G.V., ...Williams, A.C. (1998). Guidelines for the management of Parkinson's disease. Hospital Medicine, 59 (6), 469-480.
Bhatia, K., Brooks, D.J., Burn, D.J., Clarke, C.E., Playfer, J., Sawle, G.V., ...Williams, A.C. (1998). Guidelines for the management of Parkinson's disease. The Parkinson's Disease Consensus Working Group.. Hospital medicine (London, England : 1998), 59 (6), 469-480.
Dressler, D., Scaravilli, T., Bhatia, K.P., Marsden, C.D. (1998). Nicotine nasal spray is not reliable treatment for blepharospasm: Results of a pilot study. MOVEMENT DISORDERS, 13 (1), 190. doi:10.1002/mds.870130142
Bhatia, K.P., Marsden, C.D., Thomas, D.G.T. (1998). Posteroventral pallidotomy can ameliorate attacks of paroxysmal dystonia induced by exercise. Journal of Neurology, Neurosurgery and Psychiatry, 65 604-605.
Crimlisk, H.L., Bhatia, K., Cope, H., David, A., Marsden, C.D., Ron, M.A. (1998). Slater revisited: 6 year follow up study of patients with medically unexplained motor symptoms. BMJ (Clinical Research Ed.), 316 582-586.
Manji, H., Howard, R.S., Miller, D.H., Hirsch, N.P., Carr, L., Bahtia, K., ...Marsden, C.D. (1998). Status dystonicus: the syndrome and its management. Brain, 121 243-252.
Sinha, K.K., Bhatia, K.P., Sweeney, M., Davis, M.B., Banerjee, A., Jha, D.K., Wood, N. (1998). The frequency and phenotype-genotype correlation in 18 families with autosomal dominant cerebellar ataxia type 1 (ADCA-1) from Eastern India. NEUROLOGY, 50 (4), A170.
Kiriakakis, V., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1998). The natural history of tardive dystonia - A long-term follow-up study of 107 cases. Brain, 121 2053-2066.
Kiriakakis, V., Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1998). The natural history of tardive dystonia: A long term follow-up study of 107 cases. NEUROLOGY, 50 (4), A347.
Valente, E.M., Warner, T.T., Jarman, P.R., Mathen, D., Fletcher, N.A., Marsden, C.D., ...Wood, N.W. (1998). The role of DYT1 in primary torsion dystonia in Europe.. Brain, 121 (12), 2335-2339.

1997

Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1997). Clinical features and natural history of adult-onset predominantly axial dystonia. ANNALS OF NEUROLOGY, 42 (3), M57.
Bhatia, K.P., Quinn, N.P., Marsden, C.D. (1997). Clinical features and natural history of axial predominant adult onset primary dystonia. Journal of Neurology, Neurosurgery and Psychiatry, 63 788-791.
Jarman, P.R., Wood, N.W., Davis, M.T., Davis, P.V., Bhatia, K.P., Marsden, C.D., Davis, M.B. (1997). Hereditary geniospasm: Linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity. The American Journal of Human Genetics, 61 928-933.
Hanna, M.G., Bhatia, K.P. (1997). Movement disorders and mitochondrial dysfunction. Current Opinion in Neurology, 10 351-356.
Bhatia, K.P., Soland, V.L., Bhatt, M.H., Quinn, N.P., Marsden, C.D. (1997). Paroxysmal exercise-induced dystonia: Eight new sporadic cases and a review of the literature. Movement Disorders, 12 1007-1012.
Anastasopoulos, D., Bhatia, K., Bronstein, A.M., Marsden, C.D., Gresty, M.A. (1997). Perception of spatial orientation in spasmodic torticollis. Part 2: The visual vertical.. Movement Disorders, 12 (5), 709-714.
Anastasopoulos, D., Bhatia, K., Bisdorff, A., Bronstein, A.M., Gresty, M.A., Marsden, C.D. (1997). Perception of spatial orientation in spasmodic torticollis. Part I: The postural vertical.. Movement Disorders, 12 (4), 561-569.
Lekhel, H., Popov, K., Anastasopoulos, D., Bronstein, A.M., Bhatia, K.P., Marsden, C.D., Gresty, M.A. (1997). Postural responses to vibration of neck muscles in patients with idiopathic torticollis. Brain, 120 583-591.

1996

Bhatia, K.P. (1996). A case of parkinsonism associated with multiple sclerosis - Reply. MOVEMENT DISORDERS, 11 (4), 461. doi:10.1002/mds.870110427
Burn, D.J., Cartlidge, N.E.F., Bhatia, K.P., Tranchant, C., Marsden, C.D. (1996). A case of parkinsonism associated with multiple sclerosis [1]. Movement Disorders, 11 (4), 460-461. doi:10.1002/mds.870110426
Kompoliti, K., Goetz, C., Maraganore, D.M., Boeve, B.F., Marsden, C.D., Bhatia, K.P., ...Burns, R.S. (1996). Clinical presentation and pharmacological therapy in cortico-basal ganglionic degeneration. ANNALS OF NEUROLOGY, 40 (3), T171.
Soland, V.L., Bhatia, K.P., Volonte, M.A., Marsden, C.D. (1996). Focal task-specific tremors.. MOVEMENT DISORDERS, 11 (6), 665-670. doi:10.1002/mds.870110611
Soland, V.L., Bhatia, K.P., Sheean, G.L., Marsden, C.D. (1996). Hereditary geniospasm: two new families.. MOVEMENT DISORDERS, 11 (6), 744-746. doi:10.1002/mds.870110626
Bhatia, K.P., Morris, J.H., Frackowiak, R.S. (1996). Primary progressive multifocal leukoencephalopathy presenting as an extrapyramidal syndrome.. JOURNAL OF NEUROLOGY, 243 (1), 91-95.
Soland, V.L., Bhatia, K.P., Marsden, C.D. (1996). Sex prevalence of focal dystonias.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 60 (2), 204-205. doi:10.1136/jnnp.60.2.204
Bhatia, K.P., Turjanski, N., Brooks, D.J., Marsden, C.D., Thrush, D. (1996). The usefulness of functional imaging in movement disorders: an illustrative case.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 60 (3), 353-354. doi:10.1136/jnnp.60.3.353

1995

Scheffer, I.E., Bhatia, K.P., Lopes-Cendes, I., Fish, D.R., Marsden, C.D., Andermann, E., ...Cendes, F. (1995). Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder.. BRAIN, 118 61-73. doi:10.1093/brain/118.1.61
BERKOVIC, S.F., PHILLIPS, H.A., SCHEFFER, I.E., LOPESCENDES, I., BHATIA, K.P., FISH, D.R., ...SUTHERLAND, G.R. (1995). GENETIC-HETEROGENEITY IN AUTOSOMAL-DOMINANT NOCTURNAL FRONTAL-LOBE EPILEPSY. EPILEPSIA, 36 L2.
Tranchant, C., Bhatia, K.P., Marsden, C.D. (1995). Movement disorders in multiple sclerosis.. MOVEMENT DISORDERS, 10 (4), 418-423. doi:10.1002/mds.870100403
Bhatia, K.P., Brown, P., Gregory, R., Lennox, G.G., Manji, H., Thompson, P.D., ...Marsden, C.D. (1995). Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum.. BRAIN, 118 1087-1093. doi:10.1093/brain/118.5.1087
Bhatia, K.P., Marsden, C.D. (1995). Reflex sympathetic dystrophy. May be accompanied by involuntary movements.. BRITISH MEDICAL JOURNAL, 311 (7008), 811-812. doi:10.1136/bmj.311.7008.811c

1994

Scheffer, I.E., Bhatia, K.P., Lopes-Cendes, I., Fish, D.R., Marsden, C.D., Andermann, F., ...Manson, J.I. (1994). Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder.. LANCET, 343 (8896), 515-517. doi:10.1016/S0140-6736(94)91463-X
Thomas, P.K., Misra, V.P., King, R.H., Muddle, J.R., Wroe, S., Bhatia, K.P., ...Wadia, N.H. (1994). Autosomal recessive hereditary sensory neuropathy with spastic paraplegia.. BRAIN, 117 651-659. doi:10.1093/brain/117.4.651
Thompson, P.D., Bhatia, K.P., Brown, P., Davis, M.B., Pires, M., Quinn, N.P., ...Marsden, C.D. (1994). Cortical myoclonus in Huntington's disease.. MOVEMENT DISORDERS, 9 (6), 633-641. doi:10.1002/mds.870090609
Lera, G., Bhatia, K., Marsden, C.D. (1994). Dystonia as the major manifestation of Leigh's syndrome.. MOVEMENT DISORDERS, 9 (6), 642-649. doi:10.1002/mds.870090610
Bhatia, K.P., Marsden, C.D. (1994). The behavioural and motor consequences of focal lesions of the basal ganglia in man.. BRAIN, 117 859-876. doi:10.1093/brain/117.4.859
Bhatia, K.P., Lera, G., Luthert, P.J., Marsden, C.D. (1994). Vascular chorea: case report with pathology.. MOVEMENT DISORDERS, 9 (4), 447-450. doi:10.1002/mds.870090412

1993

TURJANSKI, N., BHATIA, K., BURN, D.J., SAWLE, G.V., MARSDEN, C.D., BROOKS, D.J. (1993). COMPARISON OF STRIATAL F-18 DOPA UPTAKE IN ADULT-ONSET DYSTONIA-PARKINSONISM, PARKINSONS-DISEASE, AND DOPA-RESPONSIVE DYSTONIA. NEUROLOGY, 43 (8), 1563-1568. doi:10.1212/WNL.43.8.1563
Bhatia, K.P., Daniel, S.E., Marsden, C.D. (1993). Familial parkinsonism with depression: a clinicopathological study.. ANNALS OF NEUROLOGY, 34 (6), 842-847. doi:10.1002/ana.410340614
Bhatia, K., Daniel, S.E., Marsden, C.D. (1993). Orofacial dystonia and rest tremor in a patient with normal brain pathology.. MOVEMENT DISORDERS, 8 (3), 361-362. doi:10.1002/mds.870080320
Bhatia, K.P., Bhatt, M.H., Marsden, C.D. (1993). The causalgia-dystonia syndrome.. BRAIN, 116 843-851. doi:10.1093/brain/116.4.843
Bhatia, K., Reilly, M., Adams, D., Davis, M.B., Hawkes, C.H., Thomas, P.K., ...Harding, A.E. (1993). Transthyretin gene mutations in British and French patients with amyloid neuropathy.. Journal of Neurology, Neurosurgery and Psychiatry, 56 (6), 694-697.

1992

Bhatia, K., Thompson, P.D., Marsden, C.D. (1992). "Isolated" postinfectious myoclonus.. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 55 (11), 1089-1091. doi:10.1136/jnnp.55.11.1089

1982

Pathare, A.V., Shah, S.C., Kamath, R.P., Bhatia, K.P., Mansukhani, J.R., Vakil, B.J. (1982). Pancreatic pseudocyst manifesting as massive upper gastrointestinal bleeding.. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 1 (1), 35-37.

1900

Orth, M., Schippling, S., Schneider, S.A., Bhatia, K., Talelli, P., Tabrizi, S.J., Rothwell, J. (1900). Abnormal motor cortex plasticity in premanifest and very early manifest Huntington's disease. Journal of Neurology, Neurosurgery and Psychiatry, doi:10.1136/jnnp.2009.171926
Bhatia, P.S.D.R.M.J.E.C.T.P.K.F.C.L.S.-.M.S.A.S.G.K.G.F.J.P.P.T.J.D.A.J.L.N.Q.P.M.J.C.R.K.P., Schwingenschuh, P., Ruge, D., Edwards, M.J., Terranova, C., Katschnig, P., ...Kaegi, G. (1900). Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: A clinical and electrophysiological study..
Schneider, S.A., Robertson, M.M., Rizzo, R., Turk, J., Bhatia, K., Orth, M. (1900). Fragile X syndrome associated with tic disorders. Movement Disorders,
Estevez-Fraga, C., Magrinelli, F., Latorre, A., Houlden, H., Tabrizi, S.J., Bhatia, K. (1900). Movement disorders associated with expansions and intermediate repeats in the C9orf72 gene. Presented at: MDS Virtual Congress 2020 Online conference.
Schwingenschuh, P., Katschnig, P., Saifee, T.A., Seiler, S., Aguirregomozcorta, M., Cordivari, C., ...Edwards, M.J. (1900). Moving toward "laboratory-supported" criteria for psychogenic tremor. Movement Disorders, doi:10.1002/mds.23922
Batla, A., Uchiyama, U., Simeoni, S., Melbourne, C., Baldwin, M., DeMin, L., ...Islam, S. (1900). Single-centre open label exploratory phase IIb pilot study of exogenous oral Melatonin for the treatment of Nocturia in adults with Parkinson's disease. Presented at: International Congress of Parkinson's Disease and Movement Disorders Hong Kong, HONG KONG.
Huys, A., Haggard, P., Bhatia, K., Edwards, M. (1900). The role of attention in functional movement disorders. Presented at: International Congress of Parkinson's Disease and Movement Disorders Nice, FRANCE.