Ident. | Authors (with country if any) | Title |
---|
000017 |
Maja Kojovic [Royaume-Uni] ; Panagiotis Kassavetis [Royaume-Uni] ; Matteo Bologna [Italie] ; Isabel Pareés [Royaume-Uni] ; Ignacio Rubio-Agusti [Espagne] ; Alfredo Beraredelli [Italie] ; Mark J. Edwards [Royaume-Uni] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Transcranial magnetic stimulation follow-up study in early Parkinson's disease: A decline in compensation with disease progression? |
001175 |
Ignacio Rubio-Agusti [Royaume-Uni, Espagne] ; Maja Kojovic [Royaume-Uni] ; Hoskote S. Chandrashekar [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Cervical Dystonia and Joint Hypermobility Syndrome: A Dangerous Combination |
001200 |
Ignacio Rubio-Agusti [Royaume-Uni, Espagne] ; Maja Kojovic [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Elaine Murphy [Royaume-Uni] ; Hoskote S. Chandrashekar [Royaume-Uni] ; Robin H. Lachmann [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Atypical Parkinsonism and Cerebrotendinous Xanthomatosis: Report of a Family With Corticobasal Syndrome and a Literature Review |
001335 |
Joana Damásio [Royaume-Uni, Portugal] ; Mark J. Edwards [Royaume-Uni] ; Araceli Alonso-Canovas [Royaume-Uni, Espagne] ; Petra Schwingenschuh [Royaume-Uni, Autriche] ; Georg K Gi [Royaume-Uni, Suisse] ; Kailash P. Bhatia [Royaume-Uni] | The clinical syndrome of primary tic disorder associated with dystonia: A large clinical series and a review of the literature |
001D42 |
Petra Schwingenschuh [Royaume-Uni, Autriche] ; Diane Ruge [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Carmen Terranova [Royaume-Uni] ; Petra Katschnig [Royaume-Uni, Autriche] ; Fatima Carrillo [Espagne] ; Laura Silveira-Moriyama [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni] ; Georg K Gi [Royaume-Uni] ; Francisco J. Palomar [Espagne] ; Penelope Talelli [Royaume-Uni] ; John Dickson [Royaume-Uni] ; Andrew Lees (neurologue) [Royaume-Uni] ; Niall Quinn [Royaume-Uni] ; Pablo Mir [Espagne] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Distinguishing SWEDDs patients with asymmetric resting tremor from Parkinson's disease: A clinical and electrophysiological study |
001E42 |
Araceli Alonso-Canovas [Royaume-Uni, Espagne] ; Petra Katschnig [Royaume-Uni] ; Arianna Tucci [Royaume-Uni] ; Miryam Carecchio [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Mark Edwards [Royaume-Uni] ; Juan Carlos Martínez Castrillo [Espagne] ; Derek Burke [Royaume-Uni] ; Simon Heales [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: Case report and literature review |
001F69 |
Araceli Alonso-Canovas [Royaume-Uni, Espagne] ; Petra Katschnig [Royaume-Uni] ; Arianna Tucci [Royaume-Uni] ; Miryam Carecchio [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni] ; Mark Edwards [Royaume-Uni] ; Juan Carlos Martinez Castrillo [Espagne] ; Derek Burke [Royaume-Uni] ; Simon Heales [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Atypical Parkinsonism with Apraxia and Supranuclear Gaze Abnormalities in Type 1 Gaucher Disease. Expanding the Spectrum: Case Report and Literature Review |
002296 |
Susanne A. Schneider [Royaume-Uni] ; Coro Paisan-Ruiz [Royaume-Uni] ; Ines Garcia-Gorostiaga [Royaume-Uni, Espagne] ; Niall P. Quinn [Royaume-Uni] ; Yvonne G. Weber ; Holger Lerche [Allemagne] ; John Hardy [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | GLUT1 gene mutations cause sporadic paroxysmal exercise‐induced dyskinesias |
002579 |
Nee K. Chew [Royaume-Uni] ; Pablo Mir [Royaume-Uni, Espagne] ; Mark J. Edwards [Royaume-Uni] ; Carla Cordivari [Royaume-Uni] ; Davide Martino [Royaume-Uni, Italie] ; Susanne A. Schneider [Royaume-Uni] ; Hee-Tae Kim [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | The natural history of Unverricht‐Lundborg disease: A report of eight genetically proven cases |
002669 |
Petra Schwingenschuh [Royaume-Uni, Autriche] ; Claustre Pont-Sunyer [Royaume-Uni, Espagne] ; Robert Surtees [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Psychogenic movement disorders in children: A report of 15 cases and a review of the literature |
002672 |
James T. H. Teo [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni] ; Binith J. Cheeran [Royaume-Uni] ; Miguel Fernandez-Del-Olmo [Espagne] ; Paola Giunti [Royaume-Uni] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Prolonged cortical silent period but normal sensorimotor plasticity in spinocerebellar ataxia 6 |
002C81 |
Susanne A. Schneider [Royaume-Uni] ; Mark J. Edwards [Royaume-Uni] ; Pablo Mir [Royaume-Uni, Espagne] ; Carla Cordivari [Royaume-Uni] ; Juzar Hooker [Royaume-Uni] ; John Dickson [Royaume-Uni] ; Niall Quinn [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Patients with adult‐onset dystonic tremor resembling parkinsonian tremor have scans without evidence of dopaminergic deficit (SWEDDs) |
003576 |
Davide Martino [Royaume-Uni, Italie] ; Nee-Kong Chew [Royaume-Uni, Malaisie] ; Pablo Mir [Royaume-Uni, Espagne] ; Mark J. Edwards [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Atypical movement disorders in antiphospholipid syndrome |
003598 |
Pablo Mir [Royaume-Uni, Espagne] ; Francesca Gilio [Italie] ; Mark Edwards [Royaume-Uni] ; Maurizio Inghilleri [Italie] ; Kailash P. Bhatia [Royaume-Uni] ; John C. Rothwell [Royaume-Uni] ; Niall Quinn [Royaume-Uni] | Alteration of central motor excitability in a patient with hemimasticatory spasm after treatment with botulinum toxin injections |
003607 |
Mark J. Edwards [Royaume-Uni] ; Ying-Zu Huang [Royaume-Uni, Taïwan] ; Pablo Mir [Royaume-Uni, Espagne] ; John C. Rothwell [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] | Abnormalities in motor cortical plasticity differentiate manifesting and nonmanifesting DYT1 carriers |
003A35 |
Pablo Mir [Royaume-Uni, Espagne] ; Mark J. Edwards [Royaume-Uni] ; Andrew R. J. Curtis [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni] | Adult‐onset generalized dystonia due to a mutation in the neuroferritinopathy gene |