Kailash Bhatia
Kailash Bhatia
Professor of Clinical Neurology, Institute of Neurology, UCL, Queen Square, London WC1N 3BG,
Verified email at ucl.ac.uk
Title
Cited by
Cited by
Year
Theta burst stimulation of the human motor cortex
YZ Huang, MJ Edwards, E Rounis, KP Bhatia, JC Rothwell
Neuron 45 (2), 201-206, 2005
30342005
The behavioural and motor consequences of focal lesions of the basal ganglia in man
KP Bhatia, CD Marsden
Brain 117 (4), 859-876, 1994
2583*1994
Phenomenology and classification of dystonia: a consensus update
A Albanese, K Bhatia, SB Bressman, MR DeLong, S Fahn, VSC Fung, ...
Movement disorders 28 (7), 863-873, 2013
15932013
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ...
The Lancet Neurology 7 (7), 583-590, 2008
13122008
Criteria for the diagnosis of corticobasal degeneration
MJ Armstrong, I Litvan, AE Lang, TH Bak, KP Bhatia, B Borroni, AL Boxer, ...
Neurology 80 (5), 496-503, 2013
11002013
Movement Disorders Society Scientific Issues Committee report: SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders.
I Litvan, KP Bhatia, DJ Burn, CG Goetz, AE Lang, I McKeith, N Quinn, ...
Movement disorders: official journal of the Movement Disorder Society 18 (5 …, 2003
8692003
A common LRRK2 mutation in idiopathic Parkinson's disease
WP Gilks, PM Abou-Sleiman, S Gandhi, S Jain, A Singleton, AJ Lees, ...
The Lancet 365 (9457), 415-416, 2005
8452005
Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria
GU Höglinger, G Respondek, M Stamelou, C Kurz, KA Josephs, AE Lang, ...
Movement Disorders 32 (6), 853-864, 2017
8422017
A common polymorphism in the brain‐derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS
B Cheeran, P Talelli, F Mori, G Koch, A Suppa, M Edwards, H Houlden, ...
The Journal of physiology 586 (23), 5717-5725, 2008
7042008
EFNS guidelines on diagnosis and treatment of primary dystonias
A Albanese, F Asmus, KP Bhatia, AE Elia, B Elibol, G Filippini, T Gasser, ...
European Journal of Neurology 18 (1), 5-18, 2011
4812011
Characterization of PLA2G6 as a locus for dystonia‐parkinsonism
C Paisan‐Ruiz, KP Bhatia, A Li, D Hernandez, M Davis, NW Wood, ...
Annals of neurology 65 (1), 19-23, 2009
4752009
Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society
KP Bhatia, P Bain, N Bajaj, RJ Elble, M Hallett, ED Louis, J Raethjen, ...
Movement Disorders 33 (1), 75-87, 2018
4522018
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
H Houlden, M Baker, HR Morris, N MacDonald, S Pickering–Brown, ...
Neurology 56 (12), 1702-1706, 2001
4392001
Clinical approach to Parkinson's disease: features, diagnosis, and principles of management
J Massano, KP Bhatia
Cold Spring Harbor perspectives in medicine 2 (6), a008870, 2012
4212012
Slater revisited: 6 year follow up study of patients with medically unexplained motor symptoms
HL Crimlisk, K Bhatia, H Cope, A David, CD Marsden, MA Ron
Bmj 316 (7131), 582-586, 1998
4131998
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
IE Scheffer, SF Berkovic, KP Bhatia, DR Fish, CD Marsden, ...
The Lancet 343 (8896), 515-517, 1994
3851994
A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS‐ES Task Force
A Albanese, MP Barnes, KP Bhatia, E Fernandez‐Alvarez, G Filippini, ...
European journal of neurology 13 (5), 433-444, 2006
3532006
GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak
YG Weber, A Storch, TV Wuttke, K Brockmann, J Kempfle, S Maljevic, ...
The Journal of clinical investigation 118 (6), 2157-2168, 2008
3502008
The syndrome of fixed dystonia: an evaluation of 103 patients
A Schrag, M Trimble, N Quinn, K Bhatia
Brain 127 (10), 2360-2372, 2004
3442004
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
3112014
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