Denis BrunetM.D., FRCPC

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 , p. 209.e17-209.e21, 2016, ISSN: 0197-4580.

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), p. 770-1, 2013, ISSN: 0028-3878.

| 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), p. 175-81, 2012, ISSN: 0098-7484.

Résumé | Liens:

Lemieux J, Provencher L, Brunet D, Hogue JC

Paraneoplastic encephalomyelitis, stiff person syndrome and breast carcinoma.

Can J Neurol Sci, 38 (5), p. 790-2, 2011, ISSN: 0317-1671.

| 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), p. 93-8, 2007, ISSN: 0364-5134.

Résumé | Liens: