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Neurology
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January 1, 1996
A prospective study of the clinical utility of ApoE genotype in the prediction of outcome in patients with memory impairment
M C Tierney, J P Szalai, W G Snow, et al.
Human Genetics
|
December 1, 1996
A novel mutation of presenilin 1 in familial Alzheimer's disease in Israel detected by denaturing gradient gel electrophoresis
H Reznik-Wolf, T A Treves, M Davidson, et al.
Neurology
|
October 15, 2003
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier
E Rogaeva, C Bergeron, C Sato, et al.
Annals of Neurology
|
December 16, 1998
The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease
K M Mattila, C Forsell, T Pirttilä, et al.
Neuroscience Letters
|
April 26, 1996
Three different mutations of presenilin 1 gene in early-onset Alzheimer's disease families
K Kamino, S Sato, Y Sakaki, et al.
Science (New York, N.Y.)
|
October 30, 1987
Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease
P H St George-Hyslop, R E Tanzi, R J Polinsky, et al.
Annales De Genetique
|
December 2, 1998
A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease
M G Ramirez-Dueñas, E A Rogaeva, C A Leal, et al.
Nature Genetics
|
October 1, 1993
Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes
E I Rogaev, E A Rogaeva, E K Ginter, et al.
Annals of Neurology
|
December 16, 2000
Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation
C F Lippa, V Zhukareva, T Kawarai, et al.
Neurology
|
March 1, 1990
Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity
L A Farrer, R H Myers, L A Cupples, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 72) with videos related to
Sort By:
Page
of 8
Neurology
|
January 1, 1996
A prospective study of the clinical utility of ApoE genotype in the prediction of outcome in patients with memory impairment
M C Tierney, J P Szalai, W G Snow, et al.
Human Genetics
|
December 1, 1996
A novel mutation of presenilin 1 in familial Alzheimer's disease in Israel detected by denaturing gradient gel electrophoresis
H Reznik-Wolf, T A Treves, M Davidson, et al.
Neurology
|
October 15, 2003
PS1 Alzheimer's disease family with spastic paraplegia: the search for a gene modifier
E Rogaeva, C Bergeron, C Sato, et al.
Annals of Neurology
|
December 16, 1998
The Glu318Gly mutation of the presenilin-1 gene does not necessarily cause Alzheimer's disease
K M Mattila, C Forsell, T Pirttilä, et al.
Neuroscience Letters
|
April 26, 1996
Three different mutations of presenilin 1 gene in early-onset Alzheimer's disease families
K Kamino, S Sato, Y Sakaki, et al.
Science (New York, N.Y.)
|
October 30, 1987
Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease
P H St George-Hyslop, R E Tanzi, R J Polinsky, et al.
Annales De Genetique
|
December 2, 1998
A novel Leu171Pro mutation in presenilin-1 gene in a Mexican family with early onset Alzheimer disease
M G Ramirez-Dueñas, E A Rogaeva, C A Leal, et al.
Nature Genetics
|
October 1, 1993
Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes
E I Rogaev, E A Rogaeva, E K Ginter, et al.
Annals of Neurology
|
December 16, 2000
Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation
C F Lippa, V Zhukareva, T Kawarai, et al.
Neurology
|
March 1, 1990
Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity
L A Farrer, R H Myers, L A Cupples, et al.
Page
of 8