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Journal of Medical Genetics|July 22, 2005
Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an updateG Raux, L Guyant-Maréchal, C Martin, et al.
American Journal of Human Genetics|September 9, 2000
A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31V Cormier-Daire, N Dagoneau, R Nabbout, 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.
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.
Revue Neurologique|January 1, 1989
[Retrochiasmatic lesions in multiple sclerosis. Demonstration by visual evoked potentials. Correlation with magnetic resonance imaging]M H Rigolet, C Lubetzki, C Penet, et al.
Neurology|January 1, 1995
A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterizationD Campion, A Brice, D Hannequin, et al.
American Journal of Medical Genetics|April 24, 1995
Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study GroupA Brice, S Tardieu, D Campion, et al.
American Journal of Human Genetics|October 1, 1995
Marked phenotypic heterogeneity associated with expansion of a CAG repeat sequence at the spinocerebellar ataxia 3/Machado-Joseph disease locusG Cancel, N Abbas, G Stevanin, et al.
American Journal of Human Genetics|January 1, 1994
A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusG Stevanin, E Le Guern, N Ravisé, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.
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