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, 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.

Résumé | Liens:

Rivest D, Brunet D, Desbiens R, Bouchard JP

C-5 radiculopathy as a manifestation of giant cell arteritis.

Neurology, 45 (6), 1995.

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