Rezultati pretrage - Michel Vanasse

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  1. 1
    Omega-3 fatty acid treatment of children with attention-deficit hyperactivity disorder: A randomized, double-blind, placebo-controlled study

    Omega-3 fatty acid treatment of children with attention-deficit hyperactivity disorder: A randomized, double-blind, placebo-controlled study od Stacey A Bélanger, Michel Vanasse, Schohraya Spahis, Marie‐Pierre Sylvestre, Sarah Lippé, François L’Heureux, Parviz Ghadirian, Catherine-Marie Vanasse, Émile Lévy

    Izdano 2009
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  2. 2
    Intellectual disability without epilepsy associated with STXBP1 disruption

    Intellectual disability without epilepsy associated with STXBP1 disruption od Fadi F. Hamdan, Julie Gauthier, Sylvia Dobrzeniecka, Anne Lortie, Laurent Mottron, Michel Vanasse, Guy D’Anjou, Jean Claude Lacaille, Guy A. Rouleau, Jacques L. Michaud

    Izdano 2011
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  3. 3
    Neurologic Crises in Hereditary Tyrosinemia

    Neurologic Crises in Hereditary Tyrosinemia od Grant A. Mitchell, Jean Larochelle, Marie Lambert, Jean Michaud, A Grenier, Hélène Ogier, Marie Gauthier, Jacques Lacroix, Michel Vanasse, Albert Larbrisseau, Khazal Paradis, Andrée Weber, Yolande Lefevre, Serge B. Melançon, Louis Dallaire

    Izdano 1990
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  4. 4
    Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy

    Efficacy and safety of deflazacort vs prednisone and placebo for Duchenne muscular dystrophy od Robert C. Griggs, J. Philip Miller, Cheryl R. Greenberg, Darcy Fehlings, Alan Pestronk, Jerry R. Mendell, Richard T. Moxley, Wendy King, John T. Kissel, Valerie Cwik, Michel Vanasse, Julaine Florence, Shree Pandya, Jordan Dubow, James Meyer

    Izdano 2016
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  5. 5
    Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans

    Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans od Vafa Bayat, Isabelle Thiffault, Manish Jaiswal, Martine Tétreault, Taraka Donti, Florin Sasarman, Geneviève Bernard, Julie Demers-Lamarche, Marie‐Josée Dicaire, Jean Mathieu, Michel Vanasse, Jean‐Pierre Bouchard, Marie‐France Rioux, Charles Marques Lourenço, Zhihong Li, Claire Haueter, Eric A. Shoubridge, Brett H. Graham, Bernard Brais, Hugo J. Bellen

    Izdano 2012
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  6. 6
    Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

    Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability od Fadi F. Hamdan, Julie Gauthier, Yoichi Araki, Da‐Ting Lin, Yuhki Yoshizawa, Kyohei Higashi, Areum Park, Dan Spiegelman, Sylvia Dobrzeniecka, Amélie Piton, Hideyuki Tomitori, Hussein Daoud, Christine Massicotte, Édouard Henrion, Ousmane Diallo, Masoud Shekarabi, Claude Marineau, Michael Shevell, Bruno Maranda, Grant A. Mitchell, Amélie Nadeau, Guy D’Anjou, Michel Vanasse, Myriam Srour, Ronald G. Lafrenière, Pierre Drapeau, Jean Claude Lacaille, Eunjoon Kim, Jae-Ran Lee, Kazuei Igarashi, Richard L. Huganir, Guy A. Rouleau, Jacques L. Michaud

    Izdano 2011
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