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Annals of Neurology|April 1, 1994
Eye movements in parkinsonian syndromesM Vidailhet, S Rivaud, N Gouider-Khouja, et al.
Annals of Neurology|May 1, 1989
Continuous and intermittent levodopa differentially affect basal ganglia functionJ L Juncos, T M Engber, R Raisman, et al.
Annals of Neurology|March 20, 1998
Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type IS Rivaud-Pechoux, A Dürr, B Gaymard, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
European Heart Journal|October 1, 1992
Cardiomyopathy in Friedreich's ataxia: a Doppler-echocardiographic studyD Morvan, M Komajda, L D Doan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 23, 2009
Segmental progression of early untreated Parkinson's disease: a novel approach to clinical ratingW M M Schüpbach, J-C Corvol, V Czernecki, et al.
Acta Neuropathologica|January 1, 1996
Cellular distribution of the iron-binding protein lactotransferrin in the mesencephalon of Parkinson's disease casesB Leveugle, B A Faucheux, C Bouras, et al.
The New England Journal of Medicine|October 17, 1996
Clinical and genetic abnormalities in patients with Friedreich's ataxiaA Dürr, M Cossee, Y Agid, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 23, 1999
FcepsilonRII/CD23 is expressed in Parkinson's disease and induces, in vitro, production of nitric oxide and tumor necrosis factor-alpha in glial cellsS Hunot, N Dugas, B Faucheux, et al.
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