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Publications scientifiques

  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article Lemieux J, Provencher L, Brunet D, Hogue JC

    Paraneoplastic encephalomyelitis, stiff person syndrome and breast carcinoma

    Can J Neurol Sci 38 (5), 2011.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article 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.

    DOI PUBMED
  • article Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J

    Clinical and electrophysiological study in French-Canadian population with Charcot-Marie-tooth disease type 1A associated with 17p11.2 duplication

    Can J Neurol Sci 26 (3), 1999.

    DOI PUBMED
  • article Dupré N, Bouchard JP, Cossette L, Brunet D, Vanasse M, Lemieux B, Mathon G, Puymirat J

    Phenotypic manifestations in French-Canadian populations with Charcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication

    Ann N Y Acad Sci 883 1999.

    PUBMED