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G A Nicholson

Showing results (111-120 of 115) with videos related to

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Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosisB A Hosler, G A Nicholson, P C Sapp, et al.
Neuroreport|April 14, 1997
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotypeJ B Kwok, K Taddei, M Hallupp, et al.
American Journal of Human Genetics|January 3, 2001
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyC Gaspar, I Lopes-Cendes, S Hayes, et al.
Pageof 12

Showing results (111-120 of 115) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 115 results.
Annals of Neurology|February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesisM J Smith, J B Kwok, C A McLean, et al.
Neuroscience Letters|October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in AustraliaK Taddei, D Yang, C Fisher, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosisB A Hosler, G A Nicholson, P C Sapp, et al.
Neuroreport|April 14, 1997
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotypeJ B Kwok, K Taddei, M Hallupp, et al.
American Journal of Human Genetics|January 3, 2001
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype studyC Gaspar, I Lopes-Cendes, S Hayes, et al.
Pageof 12