Search Results - Odile Russaouen

  • Showing 1 - 3 results of 3
Refine Results
  1. 1
    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 by Danielle Seilhean, Cécile Cazeneuve, Valérie Thuriès, Odile Russaouen, Stéphanie Millecamps, François Salachas, Vincent Meininger, Eric LeGuern, Charles Duyckaerts

    Published 2009
    Get full text
    Artigo
    Save to List
    Saved in:
  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 by Guilherme Riccioppo Rodrigues, Ruth H. Walker, Benedikt Bader, Adrian Danek, Alexis Brice, Cécile Cazeneuve, Odile Russaouen, Íscia Lopes‐Cendes, Wilson Marques, Vítor Tumas

    Published 2011
    Get full text Get full text
    Artigo
    Save to List
    Saved in:
  3. 3
    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 by 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

    Published 2010
    Get full text
    Artigo
    Save to List
    Saved in:

Search Tools: