Denis BrunetM.D., FRCPC

Picher-Martel V, Morin C, Brunet D, Dionne A

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

Neuromuscul Disord, 30 (8), 2020.

Résumé | Liens:

Pellerin D, Aykanat A, Ellezam B, Troiano EC, Karamchandani J, Dicaire MJ, Petitclerc M, Robertson R, Allard-Chamard X, Brunet D, Konersman CG, Mathieu J, Warman Chardon J, Gupta VA, Beggs AH, Brais B, Chrestian N

Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians

Ann Neurol, 87 (4), 2020.

Résumé | Liens:

Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orru S, Brunet D, Bouchard JP, Awadalla P, Dupre N, Dion PA, Rouleau GA

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis

Neurobiol Aging, 37 , 2016.

Résumé | Liens:

Savard M, Dupre N, Turgeon AF, Desbiens R, Langevin S, Brunet D

Propofol-related infusion syndrome heralding a mitochondrial disease: case report

Neurology, 81 (8), 2013.

| Liens:

De Wals P, Deceuninck G, Toth E, Boulianne N, Brunet D, Boucher RM, Landry M, De Serres G

Risk of Guillain-Barré syndrome following H1N1 influenza vaccination in Quebec

JAMA, 308 (2), 2012.

Résumé | Liens:

Lemieux J, Provencher L, Brunet D, Hogue JC

Paraneoplastic encephalomyelitis, stiff person syndrome and breast carcinoma

Can J Neurol Sci, 38 (5), 2011.

| Liens:

Dupre N, Chrestian N, Bouchard JP, Rossignol E, Brunet D, Sternberg D, Brais B, Mathieu J, Puymirat J

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

Neuromuscul Disord, 19 (5), 2009.

Résumé | Liens:

Dupre N, Gros-Louis F, Chrestian N, Verreault S, Brunet D, de Verteuil D, Brais B, Bouchard JP, Rouleau GA

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1

Ann Neurol, 62 (1), 2007.

Résumé | Liens:

Dionne A, Brunet D

A case of Lewis-Sumner syndrome with conduction abnormalities only in the brachial plexus and roots

Muscle Nerve, 34 (4), 2006.

Résumé | Liens:

Dionne A, Brunet D, McCampbell A, Dupre N

Adrenomyeloneuropathy: report of a new mutation in a French Canadian female

Can J Neurol Sci, 32 (2), 2005.

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