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G Stevanin

Showing results (61-70 of 81) with videos related to

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Neurology|November 30, 2006
Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystoniaI Le Ber, F Clot, L Vercueil, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
European Journal of Neurology|April 9, 2008
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genesE Panza, T Pippucci, R Cusano, et al.
Neurology|May 23, 2007
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21G Stevanin, C Paternotte, P Coutinho, et al.
Annals of Neurology|December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brainI Gourfinkel-An, G Cancel, Y Trottier, 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.
American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.
Nature Genetics|November 6, 2001
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2S E Holmes, E O'Hearn, A Rosenblatt, 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.
Genome Research|October 1, 1996
An expanded CAG repeat sequence in spinocerebellar ataxia type 7K Lindblad, M L Savontaus, G Stevanin, et al.
Pageof 9

Showing results (61-70 of 81) with videos related to

Sort By:
Pageof 9
Neurology|November 30, 2006
Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystoniaI Le Ber, F Clot, L Vercueil, et al.
Neurology|March 15, 2006
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegiaN Elleuch, C Depienne, A Benomar, et al.
European Journal of Neurology|April 9, 2008
Refinement of the SPG9 locus on chromosome 10q23.3-24.2 and exclusion of candidate genesE Panza, T Pippucci, R Cusano, et al.
Neurology|May 23, 2007
A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21G Stevanin, C Paternotte, P Coutinho, et al.
Annals of Neurology|December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brainI Gourfinkel-An, G Cancel, Y Trottier, 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.
American Journal of Human Genetics|December 1, 1996
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locusG David, P Giunti, N Abbas, et al.
Nature Genetics|November 6, 2001
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2S E Holmes, E O'Hearn, A Rosenblatt, 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.
Genome Research|October 1, 1996
An expanded CAG repeat sequence in spinocerebellar ataxia type 7K Lindblad, M L Savontaus, G Stevanin, et al.
Pageof 9