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Bernard Brais

Showing results (21-30 of 187) with videos related to

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Nature Ecology & Evolution|October 20, 2017
Mother's curse neutralizes natural selection against a human genetic disease over three centuriesEmmanuel Milot, Claudia Moreau, Alain Gagnon, et al.
Neurogenetics|July 12, 2014
A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroidsRoberta La Piana, Alina Webber, Marie-Christine Guiot, et al.
Archives of Physical Medicine and Rehabilitation|February 21, 2018
Validity and Reliability of Outcome Measures Assessing Dexterity, Coordination, and Upper Limb Strength in Autosomal Recessive Spastic Ataxia of Charlevoix-SaguenayCynthia Gagnon, Isabelle Lessard, Bernard Brais, et al.
Traffic (Copenhagen, Denmark)|August 17, 2005
Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophyAida Abu-Baker, Simon Laganiere, Xueping Fan, et al.
Faculty Reviews|March 4, 2021
POLR3-related leukodystrophy: How do mutations affecting RNA polymerase III subunits cause hypomyelination?Benoit Coulombe, Alexa Derksen, Roberta La Piana, et al.
Journal of the Neurological Sciences|May 27, 2018
Assessing mobility and balance in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay population: Validity and reliability of four outcome measuresIsabelle Lessard, Bernard Brais, Isabelle Côté, et al.
Disability and Rehabilitation. Assistive Technology|September 28, 2020
Measurement properties of wheelchair use assessment tools in adults with autosomal recessive spastic ataxia of Charlevoix-SaguenayJulie Bourassa, Krista L Best, Cynthia Gagnon, et al.
Canadian Journal of Occupational Therapy. Revue Canadienne D'Ergotherapie|April 26, 2022
Participation and Functional Independence in Adults With Recessive Spastic Ataxia of Charlevoix-SaguenaySamar Muslemani, Isabelle Lessard, Caroline Lavoie, et al.
Human Molecular Genetics|August 29, 2003
Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophyAida Abu-Baker, Christiane Messaed, Janet Laganiere, et al.
Pediatric Neurology|August 1, 2014
Vanishing white matter disease in French-Canadian patients from QuebecMarie-Ève Robinson, Elsa Rossignol, Bernard Brais, et al.
Pageof 19

Showing results (21-30 of 187) with videos related to

Sort By:
Pageof 19
Nature Ecology & Evolution|October 20, 2017
Mother's curse neutralizes natural selection against a human genetic disease over three centuriesEmmanuel Milot, Claudia Moreau, Alain Gagnon, et al.
Neurogenetics|July 12, 2014
A novel mutation in the CSF1R gene causes a variable leukoencephalopathy with spheroidsRoberta La Piana, Alina Webber, Marie-Christine Guiot, et al.
Archives of Physical Medicine and Rehabilitation|February 21, 2018
Validity and Reliability of Outcome Measures Assessing Dexterity, Coordination, and Upper Limb Strength in Autosomal Recessive Spastic Ataxia of Charlevoix-SaguenayCynthia Gagnon, Isabelle Lessard, Bernard Brais, et al.
Traffic (Copenhagen, Denmark)|August 17, 2005
Cytoplasmic targeting of mutant poly(A)-binding protein nuclear 1 suppresses protein aggregation and toxicity in oculopharyngeal muscular dystrophyAida Abu-Baker, Simon Laganiere, Xueping Fan, et al.
Faculty Reviews|March 4, 2021
POLR3-related leukodystrophy: How do mutations affecting RNA polymerase III subunits cause hypomyelination?Benoit Coulombe, Alexa Derksen, Roberta La Piana, et al.
Journal of the Neurological Sciences|May 27, 2018
Assessing mobility and balance in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay population: Validity and reliability of four outcome measuresIsabelle Lessard, Bernard Brais, Isabelle Côté, et al.
Disability and Rehabilitation. Assistive Technology|September 28, 2020
Measurement properties of wheelchair use assessment tools in adults with autosomal recessive spastic ataxia of Charlevoix-SaguenayJulie Bourassa, Krista L Best, Cynthia Gagnon, et al.
Canadian Journal of Occupational Therapy. Revue Canadienne D'Ergotherapie|April 26, 2022
Participation and Functional Independence in Adults With Recessive Spastic Ataxia of Charlevoix-SaguenaySamar Muslemani, Isabelle Lessard, Caroline Lavoie, et al.
Human Molecular Genetics|August 29, 2003
Involvement of the ubiquitin-proteasome pathway and molecular chaperones in oculopharyngeal muscular dystrophyAida Abu-Baker, Christiane Messaed, Janet Laganiere, et al.
Pediatric Neurology|August 1, 2014
Vanishing white matter disease in French-Canadian patients from QuebecMarie-Ève Robinson, Elsa Rossignol, Bernard Brais, et al.
Pageof 19