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Denis Brunet

Laval University

25

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881

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SMALED2 with BICD2 gene mutations: report of two cases and portrayal of a classical phenotype

2020 Neuromuscular Disorders
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A Novel Recessive TNNT1 Congenital Core‐Rod Myopathy in French Canadians

2020 Annals of Neurology
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Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

2016 Neurobiology of Aging
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Propofol-related infusion syndrome heralding a mitochondrial disease: case report.

2013 Neurology
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Risk of Guillain-Barré Syndrome Following H1N1 Influenza Vaccination in Quebec

2012 JAMA
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Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians

2009 Neuromuscular Disorders
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M.P.1.03 DOK7 mutations presenting as a limb girdle muscular dystrophy in French Canadians

2008 Neuromuscular Disorders
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A novel mutation in a large French-Canadian family with LGMD1B.

2008 Canadian Journal of Neurological Sciences
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G.P.10.15 Genotype–phenotype correlation and identification of new mutations in non-dystrophic myotonias

2007 Neuromuscular Disorders
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Clinical and genetic study of autosomal recessive cerebellar ataxia type 1

2007 Annals of Neurology
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Citations (76)