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Bernard Brais

Showing results (61-70 of 187) with videos related to

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Archives of Neurology|September 17, 2003
Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein geneErika Stumpf, Hélène Masson, Antoine Duquette, et al.
Anesthesia and Analgesia|January 28, 2005
Cisatracurium pharmacodynamics in patients with oculopharyngeal muscular dystrophyMarie-Josée Caron, François Girard, Dominique C Girard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 30, 2007
SPG4 founder effect in French Canadians with hereditary spastic paraplegiaInge A Meijer, Nicolas Dupré, Bernard Brais, et al.
Neurogenetics|February 27, 2016
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxiaYi-Hong Shao, Karine Choquet, Roberta La Piana, et al.
Cerebellum (London, England)|May 7, 2026
Identification of FGF14 GAA Expansions in Polish Patients with Undiagnosed Cerebellar Ataxia - A Preliminary StudyMarta Matlawska, Karolina Ziora-Jakutowicz, Marie-Josee Dicaire, et al.
Current Neurology and Neuroscience Reports|January 17, 2025
Recent Advances in the Genetics of Ataxias: An Update on Novel Autosomal Dominant Repeat ExpansionsDavid Pellerin, Pablo Iruzubieta, Isaac R L Xu, et al.
Experimental Cell Research|March 28, 2008
PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expressionArnaud F Klein, Mitsuru Ebihara, Christine Alexander, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2024
The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish PatientDilşad Türkdoğan, Natalia Smolina, Şeyma Tekgül, et al.
Disability and Rehabilitation. Assistive Technology|December 14, 2020
Wheelchair mobility, motor performance and participation of adult wheelchair users with ARSACS: a cross-sectional studyJulie Bourassa, François Routhier, Cynthia Gagnon, et al.
Annals of Neurology|May 16, 2007
Clinical and genetic study of autosomal recessive cerebellar ataxia type 1Nicolas Dupré, François Gros-Louis, Nicolas Chrestian, et al.
Pageof 19

Showing results (61-70 of 187) with videos related to

Sort By:
Pageof 19
Archives of Neurology|September 17, 2003
Adult Alexander disease with autosomal dominant transmission: a distinct entity caused by mutation in the glial fibrillary acid protein geneErika Stumpf, Hélène Masson, Antoine Duquette, et al.
Anesthesia and Analgesia|January 28, 2005
Cisatracurium pharmacodynamics in patients with oculopharyngeal muscular dystrophyMarie-Josée Caron, François Girard, Dominique C Girard, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 30, 2007
SPG4 founder effect in French Canadians with hereditary spastic paraplegiaInge A Meijer, Nicolas Dupré, Bernard Brais, et al.
Neurogenetics|February 27, 2016
Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxiaYi-Hong Shao, Karine Choquet, Roberta La Piana, et al.
Cerebellum (London, England)|May 7, 2026
Identification of FGF14 GAA Expansions in Polish Patients with Undiagnosed Cerebellar Ataxia - A Preliminary StudyMarta Matlawska, Karolina Ziora-Jakutowicz, Marie-Josee Dicaire, et al.
Current Neurology and Neuroscience Reports|January 17, 2025
Recent Advances in the Genetics of Ataxias: An Update on Novel Autosomal Dominant Repeat ExpansionsDavid Pellerin, Pablo Iruzubieta, Isaac R L Xu, et al.
Experimental Cell Research|March 28, 2008
PABPN1 polyalanine tract deletion and long expansions modify its aggregation pattern and expressionArnaud F Klein, Mitsuru Ebihara, Christine Alexander, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 20, 2024
The First Case of Autosomal Recessive Cerebellar Ataxia with Prominent Paroxysmal Non-kinesigenic Dyskinesia Caused by a Truncating FGF14 Variant in a Turkish PatientDilşad Türkdoğan, Natalia Smolina, Şeyma Tekgül, et al.
Disability and Rehabilitation. Assistive Technology|December 14, 2020
Wheelchair mobility, motor performance and participation of adult wheelchair users with ARSACS: a cross-sectional studyJulie Bourassa, François Routhier, Cynthia Gagnon, et al.
Annals of Neurology|May 16, 2007
Clinical and genetic study of autosomal recessive cerebellar ataxia type 1Nicolas Dupré, François Gros-Louis, Nicolas Chrestian, et al.
Pageof 19