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G Stevanin

Showing results (41-50 of 81) with videos related to

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Neuroscience Letters|February 12, 2000
No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24C Zander, Q P Yuan, K Lindblad, et al.
American Journal of Human Genetics|January 1, 1994
A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusG Stevanin, E Le Guern, N Ravisé, et al.
Neurology|August 1, 1994
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.
Neurology|January 13, 2006
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 yearsM Namekawa, P Ribai, I Nelson, et al.
Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.
Neurogenetics|April 13, 2015
Erratum to: The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer togetherA Duarri, E Nibbeling, M R Fokkens, et al.
Neurology|June 16, 2010
Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5pC Depienne, E Magnin, D Bouteiller, et al.
Journal of Medical Genetics|June 3, 1999
Linkage disequilibrium at the SCA2 locusO Didierjean, G Cancel, G Stevanin, et al.
Human Genetics|February 1, 1997
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1L Krols, J J Martin, G David, et al.
Pageof 9

Showing results (41-50 of 81) with videos related to

Sort By:
Pageof 9
Neuroscience Letters|February 12, 2000
No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24C Zander, Q P Yuan, K Lindblad, et al.
American Journal of Human Genetics|January 1, 1994
A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locusG Stevanin, E Le Guern, N Ravisé, et al.
Neurology|August 1, 1994
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locusS Belal, G Cancel, G Stevanin, et al.
Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.
Neurology|January 13, 2006
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 yearsM Namekawa, P Ribai, I Nelson, et al.
Neurobiology of Disease|November 1, 1994
The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14qG Stevanin, P S Sousa, G Cancel, et al.
Neurogenetics|April 13, 2015
Erratum to: The L450F [Corrected] mutation in KCND3 brings spinocerebellar ataxia and Brugada syndrome closer togetherA Duarri, E Nibbeling, M R Fokkens, et al.
Neurology|June 16, 2010
Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5pC Depienne, E Magnin, D Bouteiller, et al.
Journal of Medical Genetics|June 3, 1999
Linkage disequilibrium at the SCA2 locusO Didierjean, G Cancel, G Stevanin, et al.
Human Genetics|February 1, 1997
Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1L Krols, J J Martin, G David, et al.
Pageof 9