Movement Disorders (revue) - Corpus (PubMed)

Index « Auteurs » - entrée « Kailash P. Bhatia »
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Kailash Bhatia < Kailash P. Bhatia < Kaili M. Stanley  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 138.
[20-40] [0 - 20][0 - 50][40-60]
Ident.Authors (with country if any)Title
000884 (2013) Isabel Pareés ; Tabish A. Saifee ; Maja Kojovic ; Panagiotis Kassavetis ; Ignacio Rubio-Agusti ; Anna Sadnicka ; Kailash P. Bhatia ; Mark J. EdwardsFunctional (psychogenic) symptoms in Parkinson's disease.
000886 (2013) Maria Stamelou ; Scarlett C. Lai ; Annu Aggarwal ; Susanne A. Schneider ; Henry Houlden ; Tu-Hsueh Yeh ; Amit Batla ; Chin-Song Lu ; Mohit Bhatt ; Kailash P. BhatiaDystonic opisthotonus: a "red flag" for neurodegeneration with brain iron accumulation syndromes?
000889 (2013) Maria Stamelou ; Niall P. Quinn ; Kailash P. Bhatia"Atypical" atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide.
000903 (2013) Miryam Carecchio ; Monia Magliozzi ; Massimiliano Copetti ; Alessandro Ferraris ; Laura Bernardini ; Monica Bonetti ; Giovanni Defazio ; Mark J. Edwards ; Isabella Torrente ; Fabio Pellegrini ; Cristoforo Comi ; Kailash P. Bhatia ; Enza Maria ValenteDefining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria.
000950 (2013) Kailash P. BhatiaCommentary for "Progressive ataxia associated with scarring skin lesions and vertical gaze palsy".
000955 (2013) Maria Stamelou ; Giovanni Cossu ; Mark J. Edwards ; Daniela Murgia ; Isabel Pareés ; Maurizio Melis ; Kailash P. BhatiaFamilial psychogenic movement disorders.
000973 (2013) Antonella Macerollo ; Kailash P. BhatiaFUS gene mutations cause essential tremor: a surprise but also confirms genetic heterogeneity of essential tremor.
000A17 (2013) Maria Stamelou ; Matthew Adams ; Indran Davagnanam ; Amit Batla ; Una Sheerin ; Kevin Talbot ; Kailash P. BhatiaProgressive ataxia and palatal tremor associated with dense pontine calcification: A unique case.
000A20 (2013) Mark J. Edwards ; Anthony E. Lang ; Kailash P. BhatiaReply to Drs. Kurlan, Fasano, and Evans: A clinically useful definition of stereotypies.
000A38 (2013) Maja Kojovic ; Isabel Pareés ; Tania Lampreia ; Karolina Pienczk-Reclawowicz ; Georgia Xiromerisiou ; Ignacio Rubio-Agusti ; Milica Kramberger ; Miryam Carecchio ; Anas M. Alazami ; Francesco Brancati ; Jaroslaw Slawek ; Zvezdan Pirtosek ; Enza Maria Valente ; Fowzan S. Alkuraya ; Mark J. Edwards ; Kailash P. BhatiaThe syndrome of deafness-dystonia: clinical and genetic heterogeneity.
000A39 (2013) Amit Batla ; Maria Stamelou ; Mark J. Edwards ; Isabel Pareés ; Tabish A. Saifee ; Zoe Fox ; Kailash P. BhatiaFunctional movement disorders are not uncommon in the elderly.
000A46 (2013) Isabel Pareés ; Panagiotis Kassavetis ; Tabish A. Saifee ; Anna Sadnicka ; Marco Davare ; Kailash P. Bhatia ; John C. Rothwell ; Sven Bestmann ; Mark J. EdwardsFailure of explicit movement control in patients with functional motor symptoms.
000A68 (2013) Ignacio Rubio-Agusti ; Miryam Carecchio ; Kailash P. Bhatia ; Maja Kojovic ; Isabel Parees ; Hoskote S. Chandrashekar ; Emma J. Footitt ; Derek Burke ; Mark J. Edwards ; Robin H L. Lachmann ; Elaine MurphyMovement disorders in adult patients with classical galactosemia.
000A98 (2013) Amit Batla ; Maria Stamelou ; Niccolo Mencacci ; Anthony H. Schapira ; Kailash P. BhatiaRopinirole monotherapy induced severe reversible dyskinesias in Parkinson's disease.
000B14 (2013) Georg K Gi ; Petra Katschnig ; Mirta Fiorio ; Michele Tinazzi ; Diane Ruge ; John Rothwell ; Kailash P. BhatiaSensory tricks in primary cervical dystonia depend on visuotactile temporal discrimination.
000B17 (2012) Maja Kojovic ; Una-Marie Sheerin ; Ignacio Rubio-Agusti ; Anirban Saha ; Jose Bras ; Vaneesha Gibbons ; Rodger Palmer ; Henry Houlden ; John Hardy ; Nicholas W. Wood ; Kailash P. BhatiaYoung-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
000B42 (2013) Raquel Duran ; Niccolo E. Mencacci ; Aikaterini V. Angeli ; Maryam Shoai ; Emma Deas ; Henry Houlden ; Atul Mehta ; Derralynn Hughes ; Timothy M. Cox ; Patrick Deegan ; Anthony H. Schapira ; Andrew J. Lees ; Patricia Limousin ; Paul R. Jarman ; Kailash P. Bhatia ; Nicholas W. Wood ; John Hardy ; Tom FoltynieThe glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.
000B67 (2013) Saša R. Filipovi ; Kailash P. Bhatia ; John C. Rothwell1-Hz repetitive transcranial magnetic stimulation and diphasic dyskinesia in Parkinson's disease.
000B82 (2012) Ignacio Rubio-Agusti ; Maja Kojovic ; Mark J. Edwards ; Elaine Murphy ; Hoskote S. Chandrashekar ; Robin H. Lachmann ; Kailash P. BhatiaAtypical parkinsonism and cerebrotendinous xanthomatosis: report of a family with corticobasal syndrome and a literature review.
000C21 (2012) Alfonso Fasano ; Anabela Valadas ; Kailash P. Bhatia ; L K Prashanth ; Anthony E. Lang ; Renato P. Munhoz ; Francesca Morgante ; Daniel Tarsy ; Andrew P. Duker ; Paolo Girlanda ; Anna Rita Bentivoglio ; Alberto J. EspayPsychogenic facial movement disorders: clinical features and associated conditions.
000C70 (2012) Maria Stamelou ; Karin Tuschl ; W K Chong ; Andrew K. Burroughs ; Philippa B. Mills ; Kailash P. Bhatia ; Peter T. ClaytonDystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder.

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