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T D Bird

Showing results (181-190 of 194) with videos related to

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Archives of Neurology|November 16, 2001
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of GuamP Poorkaj, D Tsuang, E Wijsman, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
The American Journal of Pathology|June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutationsP Piccardo, J J Liepnieks, A William, et al.
Neurology|August 1, 1997
Evidence for association of HLA-A2 allele with onset age of Alzheimer's diseaseH Payami, G D Schellenberg, S Zareparsi, et al.
Science (New York, N.Y.)|December 4, 1998
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17M Hong, V Zhukareva, V Vogelsberg-Ragaglia, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Neurology|April 13, 2005
The clinical and genetic spectrum of spinocerebellar ataxia 14D-H Chen, P J Cimino, L P W Ranum, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
Nature Medicine|August 1, 1996
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's diseaseD Scheuner, C Eckman, M Jensen, et al.
The American Journal of Pathology|November 12, 1998
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genesC F Lippa, H Fujiwara, D M Mann, et al.
Pageof 20

Showing results (181-190 of 194) with videos related to

Sort By:
Pageof 20
Archives of Neurology|November 16, 2001
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of GuamP Poorkaj, D Tsuang, E Wijsman, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
The American Journal of Pathology|June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutationsP Piccardo, J J Liepnieks, A William, et al.
Neurology|August 1, 1997
Evidence for association of HLA-A2 allele with onset age of Alzheimer's diseaseH Payami, G D Schellenberg, S Zareparsi, et al.
Science (New York, N.Y.)|December 4, 1998
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17M Hong, V Zhukareva, V Vogelsberg-Ragaglia, et al.
Annals of Neurology|December 1, 1996
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsM Ikeda, V Sharma, S M Sumi, et al.
Neurology|April 13, 2005
The clinical and genetic spectrum of spinocerebellar ataxia 14D-H Chen, P J Cimino, L P W Ranum, et al.
Neurology|May 20, 2009
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.
Nature Medicine|August 1, 1996
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's diseaseD Scheuner, C Eckman, M Jensen, et al.
The American Journal of Pathology|November 12, 1998
Lewy bodies contain altered alpha-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genesC F Lippa, H Fujiwara, D M Mann, et al.
Pageof 20