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Neuroreport|July 8, 1996
A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 yearsD Campion, A Brice, C Dumanchin, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseO Didierjean, M Martinez, D Campion, et al.Brain : a Journal of Neurology|October 1, 1996
Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2A Dürr, C S Davoine, C Paternotte, et al.American Journal of Human Genetics|August 12, 1999
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrumD Campion, C Dumanchin, D Hannequin, et al.Human Genetics|November 9, 2000
The photoreceptor cell-specific nuclear receptor gene (PNR) accounts for retinitis pigmentosa in the Crypto-Jews from Portugal (Marranos), survivors from the Spanish InquisitionS Gerber, J M Rozet, S I Takezawa, et al.Nature Genetics|November 4, 2000
Mutant WD-repeat protein in triple-A syndromeA Tullio-Pelet, R Salomon, S Hadj-Rabia, et al.American Journal of Human Genetics|February 1, 1997
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexH Bickeböller, D Campion, A Brice, et al.Pageof 4