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Neurology
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February 26, 2000
Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions
A Kertesz, T Kawarai, E Rogaeva, et al.
Human Molecular Genetics
|
August 25, 2000
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance
M L Moseley, L J Schut, T D Bird, et al.
Annals of Neurology
|
January 1, 1988
Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect
T D Bird, T H Lampe, E J Nemens, et al.
Cancer
|
April 1, 1996
Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A
W D Graf, P F Chance, M W Lensch, et al.
Human Genetics
|
March 7, 1998
Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34
W H Raskind, T Bolin, J Wolff, et al.
Alzheimer Disease and Associated Disorders
|
January 1, 1993
Lack of detectable radiation hypersensitivity in lymphoblastoid cells from multiple pedigrees of familial Alzheimer disease
E M Bryant, T D Bird, C E Ogburn, et al.
Nature Genetics
|
January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA
M D Koob, K A Benzow, T D Bird, et al.
Neuroreport
|
February 23, 2000
Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism
K Furukawa, I D'Souza, C H Crudder, et al.
Neurology
|
July 1, 1989
Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome
D Nochlin, S M Sumi, T D Bird, et al.
American Journal of Human Genetics
|
January 13, 2000
The number of trait loci in late-onset Alzheimer disease
E W Daw, H Payami, E J Nemens, et al.
Page
of 20
Search research articles
Search
Showing results (121-130 of 194) with videos related to
Sort By:
Page
of 20
Neurology
|
February 26, 2000
Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions
A Kertesz, T Kawarai, E Rogaeva, et al.
Human Molecular Genetics
|
August 25, 2000
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance
M L Moseley, L J Schut, T D Bird, et al.
Annals of Neurology
|
January 1, 1988
Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect
T D Bird, T H Lampe, E J Nemens, et al.
Cancer
|
April 1, 1996
Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A
W D Graf, P F Chance, M W Lensch, et al.
Human Genetics
|
March 7, 1998
Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34
W H Raskind, T Bolin, J Wolff, et al.
Alzheimer Disease and Associated Disorders
|
January 1, 1993
Lack of detectable radiation hypersensitivity in lymphoblastoid cells from multiple pedigrees of familial Alzheimer disease
E M Bryant, T D Bird, C E Ogburn, et al.
Nature Genetics
|
January 13, 1998
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA
M D Koob, K A Benzow, T D Bird, et al.
Neuroreport
|
February 23, 2000
Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism
K Furukawa, I D'Souza, C H Crudder, et al.
Neurology
|
July 1, 1989
Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome
D Nochlin, S M Sumi, T D Bird, et al.
American Journal of Human Genetics
|
January 13, 2000
The number of trait loci in late-onset Alzheimer disease
E W Daw, H Payami, E J Nemens, et al.
Page
of 20