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O Didierjean

Showing results (1-10 of 14) with videos related to

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Human Mutation|February 5, 1998
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph diseaseG Cancel, I Gourfinkel-An, G Stevanin, et al.
Brain : a Journal of Neurology|October 1, 1996
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3K Bürk, M Abele, M Fetter, et al.
Journal of Neurology|April 1, 1997
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locusK Bürk, G Stevanin, O Didierjean, et al.
Neurology|December 31, 1997
Clinical and molecular features of spinocerebellar ataxia type 6G Stevanin, A Dürr, G David, et al.
Human Molecular Genetics|December 1, 1995
Mutations of the presenilin I gene in families with early-onset Alzheimer's diseaseD Campion, J M Flaman, A Brice, et al.
Journal of Medical Genetics|June 3, 1999
Linkage disequilibrium at the SCA2 locusO Didierjean, G Cancel, G Stevanin, et al.
Archives of Neurology|June 17, 1998
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer diseaseM Martinez, D Campion, A Brice, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Nature Genetics|November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsG Imbert, F Saudou, G Yvert, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseO Didierjean, M Martinez, D Campion, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Human Mutation|February 5, 1998
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph diseaseG Cancel, I Gourfinkel-An, G Stevanin, et al.
Brain : a Journal of Neurology|October 1, 1996
Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3K Bürk, M Abele, M Fetter, et al.
Journal of Neurology|April 1, 1997
Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locusK Bürk, G Stevanin, O Didierjean, et al.
Neurology|December 31, 1997
Clinical and molecular features of spinocerebellar ataxia type 6G Stevanin, A Dürr, G David, et al.
Human Molecular Genetics|December 1, 1995
Mutations of the presenilin I gene in families with early-onset Alzheimer's diseaseD Campion, J M Flaman, A Brice, et al.
Journal of Medical Genetics|June 3, 1999
Linkage disequilibrium at the SCA2 locusO Didierjean, G Cancel, G Stevanin, et al.
Archives of Neurology|June 17, 1998
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer diseaseM Martinez, D Campion, A Brice, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Nature Genetics|November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsG Imbert, F Saudou, G Yvert, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's diseaseO Didierjean, M Martinez, D Campion, et al.
Pageof 2