Recherche clinique sur les maladies neuro-musculaires telles polyneuropathies inflammatoires ou diabétiques, myosites, sclérose latérale amyotrophique.
Québec, Québec
Canada G1J 1Z4
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SMALED2 with BICD2 gene mutations: Report of two cases and portrayal of a classical phenotype
Article de revueNeuromuscul Disord, 30 (8), 2020.
Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians
Article de revueAnn Neurol, 87 (4), 2020.
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
Article de revueNeurobiol Aging, 37 , 2016.
Propofol-related infusion syndrome heralding a mitochondrial disease: case report
Article de revueNeurology, 81 (8), 2013.
Risk of Guillain-Barré syndrome following H1N1 influenza vaccination in Quebec
Article de revueJAMA, 308 (2), 2012.
Paraneoplastic encephalomyelitis, stiff person syndrome and breast carcinoma
Article de revueCan J Neurol Sci, 38 (5), 2011.
Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians
Article de revueNeuromuscul Disord, 19 (5), 2009.
Clinical and genetic study of autosomal recessive cerebellar ataxia type 1
Article de revueAnn Neurol, 62 (1), 2007.
A case of Lewis-Sumner syndrome with conduction abnormalities only in the brachial plexus and roots
Article de revueMuscle Nerve, 34 (4), 2006.
Adrenomyeloneuropathy: report of a new mutation in a French Canadian female
Article de revueCan J Neurol Sci, 32 (2), 2005.