Search Results - Nigaud, K.

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    Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study by Moss, Davina, Pardiñas, Antonio, Langbehn, Douglas, Lo, Kitty, Leavitt, Blair, Roos, Raymund, Durr, Alexandra, Mead, Simon, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah, Coleman, A, Santos, R Dar, Decolongon, J, Sturrock, A, Bardinet, E, Ret, C Jauff, Justo, D, Lehericy, S, Marelli, C, Nigaud, K, Valabrègue, R, van den Bogaard, Sja, Dumas, E, van der Grond, J, t'Hart, Ep, Jurgens, C, Witjes-Ane, M-N, Arran, N, Callaghan, J, Stopford, C, Frost, C, Jones, R, Hobbs, N, Lahiri, N, Ordidge, R, Owen, G, Pepple, T, Read, J, Say, M, Wild, E, Patel, A, Fox, N, Gibbard, C, Malone, I, Crawford, H, Whitehead, D, Keenan, S, Cash, D, Berna, C, Bechtel, N, Bohlen, S, Man, a Hoff, Kraus, P, Axelson, E, Wang, C, Acharya, T, Lee, S, Monaco, W, Campbell, C, Queller, S, Whitlock, K, Campbell, M, Frajman, E, Milchman, C, O'Regan, A, Labuschagne, I, Stout, J, Landwehrmeyer, B, Craufurd, D, Scahill, R, Hicks, S, Kennard, C, Johnson, H, Tobin, A, Rosas, Hd, Reilmann, R, Borowsky, B, Pourchot, C, Andrews, S, Bachoud-Lévi, Anne-Catherine, Bentivoglio, Anna Rita, Biunno, Ida, Bonelli, Raphael, Burgunder, Jean-Marc, Dunnett, Stephen, Ferreira, Joaquim, Handley, Olivia, Heiberg, Arvid, Illmann, Torsten, Landwehrmeyer, G. Bernhard, Levey, Jamie, Ramos-Arroyo, Maria, Nielsen, Jørgen, Koivisto, Susana Pro, Päivärinta, Markku, Roos, Raymund A.C., Sebastián, a Rojo, Vandenberghe, Wim, Verellen-Dumoulin, Christine

    Published in Lancet neurology
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