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Bernard Brais

Showing results (1-10 of 187) with videos related to

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Current Neurology and Neuroscience Reports|December 17, 2008
Oculopharyngeal muscular dystrophy: a polyalanine myopathyBernard Brais
Neurogenetics|January 9, 2015
A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxiaKarine Choquet, Roberta La Piana, Bernard Brais
Orbit (Amsterdam, Netherlands)|June 5, 2002
Oculopharyngeal muscular dystrophy: What's new?François Codère, Bernard Brais, Guy Rouleau, et al.
Orphanet Journal of Rare Diseases|October 1, 2022
Documenting manifestations and impacts of autosomal recessive spastic ataxia of Charlevoix-Saguenay to develop patient-reported outcomeMarjolaine Tremblay, Laura Girard-Côté, Bernard Brais, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2013
Clinical presentation and early evolution of spastic ataxia of Charlevoix-SaguenayAntoine Duquette, Bernard Brais, Jean-Pierre Bouchard, et al.
Journal of Child Neurology|November 9, 2014
Myelination Delay and Allan-Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 GeneRoberta La Piana, Michel Vanasse, Bernard Brais, et al.
Archives of Neurology|March 28, 2012
4H syndrome with late-onset growth hormone deficiency caused by POLR3A mutationsAna Potic, Bernard Brais, Karine Choquet, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|July 22, 2021
Cross-cultural adaptation of the SWAL-QOL and the Sydney Swallow Questionnaire (SSQ) into French-Canadian and preliminary assessment for their use in an oculopharyngeal muscular dystrophy (OPMD) populationClaudia Côté, Julie Fortin, Bernard Brais, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|January 29, 2020
Neurological Involvement in Glycogen Storage Disease Type IXa due to <i>PHKA2</i> MutationChelsea Smith, , Marie-Josée Dicaire, et al.
Muscle & Nerve|December 22, 2018
The requirement for a disease-specific patient-reported outcome measure of dysphagia in oculopharyngeal muscular dystrophyClaudia Côté, Cynthia Gagnon, Sarah Youssof, et al.
Pageof 19

Showing results (1-10 of 187) with videos related to

Sort By:
Pageof 19
Current Neurology and Neuroscience Reports|December 17, 2008
Oculopharyngeal muscular dystrophy: a polyalanine myopathyBernard Brais
Neurogenetics|January 9, 2015
A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxiaKarine Choquet, Roberta La Piana, Bernard Brais
Orbit (Amsterdam, Netherlands)|June 5, 2002
Oculopharyngeal muscular dystrophy: What's new?François Codère, Bernard Brais, Guy Rouleau, et al.
Orphanet Journal of Rare Diseases|October 1, 2022
Documenting manifestations and impacts of autosomal recessive spastic ataxia of Charlevoix-Saguenay to develop patient-reported outcomeMarjolaine Tremblay, Laura Girard-Côté, Bernard Brais, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 2013
Clinical presentation and early evolution of spastic ataxia of Charlevoix-SaguenayAntoine Duquette, Bernard Brais, Jean-Pierre Bouchard, et al.
Journal of Child Neurology|November 9, 2014
Myelination Delay and Allan-Herndon-Dudley Syndrome Caused by a Novel Mutation in the SLC16A2 GeneRoberta La Piana, Michel Vanasse, Bernard Brais, et al.
Archives of Neurology|March 28, 2012
4H syndrome with late-onset growth hormone deficiency caused by POLR3A mutationsAna Potic, Bernard Brais, Karine Choquet, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|July 22, 2021
Cross-cultural adaptation of the SWAL-QOL and the Sydney Swallow Questionnaire (SSQ) into French-Canadian and preliminary assessment for their use in an oculopharyngeal muscular dystrophy (OPMD) populationClaudia Côté, Julie Fortin, Bernard Brais, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|January 29, 2020
Neurological Involvement in Glycogen Storage Disease Type IXa due to <i>PHKA2</i> MutationChelsea Smith, , Marie-Josée Dicaire, et al.
Muscle & Nerve|December 22, 2018
The requirement for a disease-specific patient-reported outcome measure of dysphagia in oculopharyngeal muscular dystrophyClaudia Côté, Cynthia Gagnon, Sarah Youssof, et al.
Pageof 19