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B Brais

Showing results (1-10 of 38) with videos related to

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Cytogenetic and Genome Research|October 4, 2003
Oculopharyngeal muscular dystrophy: a late-onset polyalanine diseaseB Brais
Brain and Language|November 1, 1993
Jean Martin Charcot and aphasia: treading the line between experimental physiology and pathological anatomyB Brais
Human Molecular Genetics|November 2, 2001
Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell deathX Fan, P Dion, J Laganiere, et al.
Revue Neurologique|April 12, 2024
Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxiaG Clément, S Puisieux, D Pellerin, et al.
Molecular Genetics and Genomics : MGG|July 30, 2025
Loss of dcst2 expression in male zebrafish is not associated with muscle hypertrophyX Allard-Chamard, E C Rodríguez, B Brais, et al.
Neuromuscular Disorders : NMD|August 28, 2007
Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiationS A Nahas, A Duquette, K Roddier, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Recent studies on oculopharyngeal muscular dystrophy in QuébecJ P Bouchard, B Brais, D Brunet, et al.
Seminars in Neurology|March 11, 2000
Oculopharyngeal muscular dystrophyB Brais, G A Rouleau, J P Bouchard, et al.
Annals of Neurology|November 18, 2000
PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophyV Shanmugam, P Dion, D Rochefort, et al.
Revue Neurologique|March 18, 2008
[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada]N Dupré, N Chrestian, I Thiffault, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Cytogenetic and Genome Research|October 4, 2003
Oculopharyngeal muscular dystrophy: a late-onset polyalanine diseaseB Brais
Brain and Language|November 1, 1993
Jean Martin Charcot and aphasia: treading the line between experimental physiology and pathological anatomyB Brais
Human Molecular Genetics|November 2, 2001
Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell deathX Fan, P Dion, J Laganiere, et al.
Revue Neurologique|April 12, 2024
Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxiaG Clément, S Puisieux, D Pellerin, et al.
Molecular Genetics and Genomics : MGG|July 30, 2025
Loss of dcst2 expression in male zebrafish is not associated with muscle hypertrophyX Allard-Chamard, E C Rodríguez, B Brais, et al.
Neuromuscular Disorders : NMD|August 28, 2007
Ataxia-oculomotor apraxia 2 patients show no increased sensitivity to ionizing radiationS A Nahas, A Duquette, K Roddier, et al.
Neuromuscular Disorders : NMD|December 10, 1997
Recent studies on oculopharyngeal muscular dystrophy in QuébecJ P Bouchard, B Brais, D Brunet, et al.
Seminars in Neurology|March 11, 2000
Oculopharyngeal muscular dystrophyB Brais, G A Rouleau, J P Bouchard, et al.
Annals of Neurology|November 18, 2000
PABP2 polyalanine tract expansion causes intranuclear inclusions in oculopharyngeal muscular dystrophyV Shanmugam, P Dion, D Rochefort, et al.
Revue Neurologique|March 18, 2008
[Hereditary ataxias, spastic parapareses and neuropathies in Eastern Canada]N Dupré, N Chrestian, I Thiffault, et al.
Pageof 4