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The New England Journal of Medicine|May 29, 2000
Association between early-onset Parkinson's disease and mutations in the parkin geneC B Lücking, A Dürr, V Bonifati, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
A refined physical and transcriptional map of the SPG9 locus on 10q23.3-q24.2C Lo Nigro, R Cusano, M Scaranari, et al.
Human Molecular Genetics|August 1, 1997
The Friedreich ataxia GAA triplet repeat: premutation and normal allelesL Montermini, E Andermann, M Labuda, et al.
Journal of Neurology|August 4, 1999
Spinocerebellar ataxia type 2 in southern Italy: a clinical and molecular study of 30 familiesA Filla, G De Michele, L Santoro, et al.
Neurology|December 15, 2004
Imaging of dopaminergic dysfunction with [123I]FP-CIT SPECT in early-onset parkin diseaseA Varrone, M T Pellecchia, M Amboni, et al.
Journal of Neurology|November 5, 2015
Powerhouse failure and oxidative damage in autosomal recessive spastic ataxia of Charlevoix-SaguenayChiara Criscuolo, C Procaccini, M C Meschini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
Epidemiology of progressive supranuclear palsy. ESGAP Consortium. European Study Group on Atypical ParkinsonismsN Vanacore, V Bonifati, C Colosimo, et al.
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