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Y Agid

Showing results (411-420 of 611) with videos related to

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Nature Genetics|January 1, 1994
Is DRPLA also linked to 14q?G Cancel, A Dürr, G Stevanin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.
Revue Neurologique|December 1, 1995
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]D Hannequin, D Campion, S Tardieu, et al.
Journal of Medical Genetics|October 1, 1995
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseG Stevanin, E Cassa, G Cancel, 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.
Neuromuscular Disorders : NMD|September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the geneE Le Guern, N Ravise, M Gugenheim, et al.
Clinical Neuropharmacology|January 1, 1986
Parkinson's disease and dementiaY Agid, M Ruberg, B Dubois, et al.
Pageof 62

Showing results (411-420 of 611) with videos related to

Sort By:
Pageof 62
Nature Genetics|January 1, 1994
Is DRPLA also linked to 14q?G Cancel, A Dürr, G Stevanin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.
Revue Neurologique|December 1, 1995
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]D Hannequin, D Campion, S Tardieu, et al.
Journal of Medical Genetics|October 1, 1995
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseG Stevanin, E Cassa, G Cancel, 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.
Neuromuscular Disorders : NMD|September 1, 1994
Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the geneE Le Guern, N Ravise, M Gugenheim, et al.
Clinical Neuropharmacology|January 1, 1986
Parkinson's disease and dementiaY Agid, M Ruberg, B Dubois, et al.
Pageof 62