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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Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians.
Article de revueAnn Neurol, 87 (4), p. 568-583, 2020, ISSN: 0364-5134.
SMALED2 with BICD2 gene mutations: Report of two cases and portrayal of a classical phenotype.
Article de revueNeuromuscul Disord, 30 (8), p. 669-673, 2020, ISSN: 0960-8966.
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.
Article de revueNeurobiol Aging, 37 , p. 209.e17-209.e21, 2016, ISSN: 0197-4580.
Propofol-related infusion syndrome heralding a mitochondrial disease: case report.
Article de revueNeurology, 81 (8), p. 770-1, 2013, ISSN: 0028-3878.
Risk of Guillain-Barré syndrome following H1N1 influenza vaccination in Quebec.
Article de revueJAMA, 308 (2), p. 175-81, 2012, ISSN: 0098-7484.
Paraneoplastic encephalomyelitis, stiff person syndrome and breast carcinoma.
Article de revueCan J Neurol Sci, 38 (5), p. 790-2, 2011, ISSN: 0317-1671.
Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.
Article de revueAnn Neurol, 62 (1), p. 93-8, 2007, ISSN: 0364-5134.
A case of Lewis-Sumner syndrome with conduction abnormalities only in the brachial plexus and roots.
Article de revueMuscle Nerve, 34 (4), p. 489-93, 2006, ISSN: 0148-639X.
Adrenomyeloneuropathy: report of a new mutation in a French Canadian female.
Article de revueCan J Neurol Sci, 32 (2), p. 261-3, 2005, ISSN: 0317-1671.
C-5 radiculopathy as a manifestation of giant cell arteritis.
Article de revueNeurology, 45 (6), p. 1222-4, 1995, ISSN: 0028-3878.