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G Stevanin

Showing results (11-20 of 81) with videos related to

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Journal of Medical Genetics|November 1, 1992
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research GroupA Brice, N Ravisé, G Stevanin, et al.
Nature Genetics|March 4, 2000
Are (CTG)n expansions at the SCA8 locus rare polymorphisms?G Stevanin, A Herman, A Dürr, et al.
Acta Neurologica Scandinavica|March 26, 2011
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG geneJ Koht, G Stevanin, A Durr, et al.
Human Molecular Genetics|September 16, 1998
De novo expansion of intermediate alleles in spinocerebellar ataxia 7G Stevanin, P Giunti, G D Belal, et al.
Nature Genetics|October 1, 1995
Gender equality in Machado-Joseph diseaseA Dürr, G Stevanin, G Cancel, et al.
Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.
Revue Neurologique|November 1, 1995
[Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families]O Dubourg, A Dürr, H Chneiweiss, et al.
Annals of Neurology|February 1, 1995
Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlationsO Dubourg, A Dürr, G Cancel, et al.
Human Molecular Genetics|September 1, 1993
Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1G Cancel, C Khati, G Stevanin, et al.
Psychiatry Research|October 23, 1997
A preliminary study on early onset schizophrenia and bipolar disorder: large polyglutamine expansions are not involvedF Schürhoff, G Stevanin, Y Trottier, et al.
Pageof 9

Showing results (11-20 of 81) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|November 1, 1992
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research GroupA Brice, N Ravisé, G Stevanin, et al.
Nature Genetics|March 4, 2000
Are (CTG)n expansions at the SCA8 locus rare polymorphisms?G Stevanin, A Herman, A Dürr, et al.
Acta Neurologica Scandinavica|March 26, 2011
SCA14 in Norway, two families with autosomal dominant cerebellar ataxia and a novel mutation in the PRKCG geneJ Koht, G Stevanin, A Durr, et al.
Human Molecular Genetics|September 16, 1998
De novo expansion of intermediate alleles in spinocerebellar ataxia 7G Stevanin, P Giunti, G D Belal, et al.
Nature Genetics|October 1, 1995
Gender equality in Machado-Joseph diseaseA Dürr, G Stevanin, G Cancel, et al.
Brain : a Journal of Neurology|December 1, 1993
Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneityA Dürr, H Chneiweiss, C Khati, et al.
Revue Neurologique|November 1, 1995
[Does the ataxo-choreic form of DRPLA exist in Europe? Search of mutation in 120 families]O Dubourg, A Dürr, H Chneiweiss, et al.
Annals of Neurology|February 1, 1995
Analysis of the SCA1 CAG repeat in a large number of families with dominant ataxia: clinical and molecular correlationsO Dubourg, A Dürr, G Cancel, et al.
Human Molecular Genetics|September 1, 1993
Endothelin 1 is not a candidate gene for spinal cerebellar ataxia 1G Cancel, C Khati, G Stevanin, et al.
Psychiatry Research|October 23, 1997
A preliminary study on early onset schizophrenia and bipolar disorder: large polyglutamine expansions are not involvedF Schürhoff, G Stevanin, Y Trottier, et al.
Pageof 9