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Journal of the Neurological Sciences|April 23, 2017
Xeroderma pigmentosum complementation group F: A rare cause of cerebellar ataxia with choreaG Carré, C Marelli, M Anheim, et al.Revue Neurologique|April 29, 2008
[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature]M Anheim, D Chaigne, M Fleury, et al.Journal of Neurology|June 30, 2018
Prospective study of relevance of 123I-MIBG myocardial scintigraphy and clonidine GH test to distinguish Parkinson's disease and multiple system atrophyC Alves Do Rego, I J Namer, C Marcel, et al.Revue Neurologique|June 23, 2019
Introduction and classical environmental risk factors for ParkinsonC TranchantRevue Neurologique|January 5, 2001
[Focal dystonia: clinical, etiologic and therapeutic aspects]C TranchantRevue Neurologique|March 5, 2013
[Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?]C TranchantRevue Neurologique|November 28, 2006
[What is the role of other complementary examination in amyotrophic lateral sclerosis?]C TranchantHandbook of Experimental Pharmacology|January 6, 2007
Conditional mouse models for Friedreich ataxia, a neurodegenerative disorder associating cardiomyopathyH PuccioPageof 17