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
29592005
The behavioural and motor consequences of focal lesions of the basal ganglia in man
KP Bhatia, CD Marsden
Brain 117 (4), 859-876, 1994
2566*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
15232013
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
12852008
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
10522013
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
8592003
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
8332005
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
7672017
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
6912008
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
4672009
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
4652011
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
4302001
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
4172018
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
4091998
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
3982012
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
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
3472008
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
3472006
The syndrome of fixed dystonia: an evaluation of 103 patients
A Schrag, M Trimble, N Quinn, K Bhatia
Brain 127 (10), 2360-2372, 2004
3382004
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
3002014
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