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Annals of Neurology|September 1, 1994
Phenotype of chromosome 14-linked familial Alzheimer's disease in a large kindredT H Lampe, T D Bird, D Nochlin, et al.Journal of the American Geriatrics Society|May 14, 1999
Clinico-neuropathological correlation of Alzheimer's disease in a community-based case seriesA Lim, D Tsuang, W Kukull, et al.Science (New York, N.Y.)|September 16, 1988
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.Brain : a Journal of Neurology|September 1, 1999
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factorsT Gómez-Isla, W B Growdon, M J McNamara, et al.Archives of Neurology|March 20, 2001
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementiaP Poorkaj, M Grossman, E Steinbart, et al.Annals of Neurology|June 1, 1997
Presenilin-1 protein expression in familial and sporadic Alzheimer's diseaseA I Levey, C J Heilman, J J Lah, et al.Annals of Neurology|August 1, 1996
Amyloid beta protein (Abeta) deposition in chromosome 14-linked Alzheimer's disease: predominance of Abeta42(43)D M Mann, T Iwatsubo, N J Cairns, et al.The American Journal of Pathology|July 1, 1996
High levels of circulating beta-amyloid peptide do not cause cerebral beta-amyloidosis in transgenic miceK Fukuchi, L Ho, S G Younkin, et al.Archives of Neurology|December 11, 1999
The utility of apolipoprotein E genotyping in the diagnosis of Alzheimer disease in a community-based case seriesD Tsuang, E B Larson, J Bowen, et al.Pageof 7