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G Stevanin

Showing results (51-60 of 81) with videos related to

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Clinical Genetics|May 15, 2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneityA Boukhris, G Stevanin, I Feki, et al.
Brain : a Journal of Neurology|September 26, 2001
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxiaH Fujigasaki, J J Martin, P P De Deyn, et al.
Neurology|June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?P Charles, A Camuzat, N Benammar, et al.
American Journal of Human Genetics|May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardationA Herman-Bert, G Stevanin, J C Netter, et al.
European Journal of Neurology|July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormalityN Collongues, C Depienne, N Boehm, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1996
Mutation detection in Machado-Joseph disease using repeat expansion detectionK Lindblad, A Lunkes, P Maciel, et al.
Neurology|March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German familiesM Dichgans, L Schöls, J Herzog, et al.
Human Molecular Genetics|August 11, 1999
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysisR P Grewal, G Cancel, E P Leeflang, et al.
Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.
Human Genetics|May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 familiesA Lezin, G Cancel, G Stevanin, et al.
Pageof 9

Showing results (51-60 of 81) with videos related to

Sort By:
Pageof 9
Clinical Genetics|May 15, 2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneityA Boukhris, G Stevanin, I Feki, et al.
Brain : a Journal of Neurology|September 26, 2001
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxiaH Fujigasaki, J J Martin, P P De Deyn, et al.
Neurology|June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?P Charles, A Camuzat, N Benammar, et al.
American Journal of Human Genetics|May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardationA Herman-Bert, G Stevanin, J C Netter, et al.
European Journal of Neurology|July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormalityN Collongues, C Depienne, N Boehm, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1996
Mutation detection in Machado-Joseph disease using repeat expansion detectionK Lindblad, A Lunkes, P Maciel, et al.
Neurology|March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German familiesM Dichgans, L Schöls, J Herzog, et al.
Human Molecular Genetics|August 11, 1999
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysisR P Grewal, G Cancel, E P Leeflang, et al.
Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.
Human Genetics|May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 familiesA Lezin, G Cancel, G Stevanin, et al.
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