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B Brais

Showing results (31-40 of 38) with videos related to

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Brain : a Journal of Neurology|May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34I Thiffault, M F Rioux, M Tetreault, et al.
Neurology|November 23, 2000
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneS C Blumen, A D Korczyn, H Lavoie, et al.
Neurology|May 25, 2005
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French CanadiansK Roddier, T Thomas, G Marleau, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 20, 2012
Diversity of ARSACS mutations in French-CanadiansI Thiffault, M J Dicaire, M Tetreault, et al.
Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.
Journal of Child Neurology|July 29, 2020
Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot StudyE Dermer, A Spahr, L T Tran, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Journal of Neuromuscular Diseases|September 14, 2020
The Canadian Neuromuscular Disease Registry 2010-2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease RegistryV Hodgkinson, J Lounsberry, S M'Dahoma, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Brain : a Journal of Neurology|May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34I Thiffault, M F Rioux, M Tetreault, et al.
Neurology|November 23, 2000
Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 geneS C Blumen, A D Korczyn, H Lavoie, et al.
Neurology|May 25, 2005
Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French CanadiansK Roddier, T Thomas, G Marleau, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 20, 2012
Diversity of ARSACS mutations in French-CanadiansI Thiffault, M J Dicaire, M Tetreault, et al.
Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.
Journal of Child Neurology|July 29, 2020
Stress in Parents of Children With Genetically Determined Leukoencephalopathies: A Pilot StudyE Dermer, A Spahr, L T Tran, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Journal of Neuromuscular Diseases|September 14, 2020
The Canadian Neuromuscular Disease Registry 2010-2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease RegistryV Hodgkinson, J Lounsberry, S M'Dahoma, et al.
Pageof 4