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P H St George-Hyslop

Showing results (31-40 of 72) with videos related to

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Neurology|January 1, 1996
A prospective study of the clinical utility of ApoE genotype in the prediction of outcome in patients with memory impairmentM 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 electrophoresisH 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 modifierE 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 diseaseK 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 familiesK 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 diseaseP 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 diseaseM 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 genesE 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 mutationC 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 heterogeneityL A Farrer, R H Myers, L A Cupples, et al.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
Neurology|January 1, 1996
A prospective study of the clinical utility of ApoE genotype in the prediction of outcome in patients with memory impairmentM 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 electrophoresisH 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 modifierE 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 diseaseK 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 familiesK 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 diseaseP 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 diseaseM 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 genesE 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 mutationC 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 heterogeneityL A Farrer, R H Myers, L A Cupples, et al.
Pageof 8