检索结果 - Odile Russaouen

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    Accumulation of TDP-43 and α-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation

    Accumulation of TDP-43 and α-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation 由 Danielle Seilhean, Cécile Cazeneuve, Valérie Thuriès, Odile Russaouen, Stéphanie Millecamps, François Salachas, Vincent Meininger, Eric LeGuern, Charles Duyckaerts

    出版 2009
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  2. 2
    Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype

    Clinical and genetic analysis of 29 Brazilian patients with Huntington's disease-like phenotype 由 Guilherme Riccioppo Rodrigues, Ruth H. Walker, Benedikt Bader, Adrian Danek, Alexis Brice, Cécile Cazeneuve, Odile Russaouen, Íscia Lopes‐Cendes, Wilson Marques, Vítor Tumas

    出版 2011
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    SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations

    SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations 由 Stéphanie Millecamps, François Salachas, C. Cazeneuve, Gordon Gilbert, Bernard Bricka, A. Camuzat, Léna Guillot‐Noël, Odile Russaouen, Gaëlle Bruneteau, Pierre‐François Pradat, Nadine Le Forestier, N. Vandenberghe, Véronique Danel-Brunaud, Nathalie Guy, Christel Thauvin-Robinet, Lucette Lacomblez, P. Couratier, Didier Hannequin, Danielle Seilhean, Isabelle Le Ber, P. Corcia, William Camu, Alexis Brice, Guy A. Rouleau, Eric Leguern, Vincent Meininger

    出版 2010
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