Works matching IS 09646906 AND DT 2014 AND VI 23 AND IP 3


Results: 26
    1

    Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. 749, doi. 10.1093/hmg/ddt460
    By:
    • Dols-Icardo, Oriol;
    • García-Redondo, Alberto;
    • Rojas-García, Ricard;
    • Sánchez-Valle, Raquel;
    • Noguera, Aina;
    • Gómez-Tortosa, Estrella;
    • Pastor, Pau;
    • Hernández, Isabel;
    • Esteban-Pérez, Jesús;
    • Suárez-Calvet, Marc;
    • Antón-Aguirre, Sofía;
    • Amer, Guillermo;
    • Ortega-Cubero, Sara;
    • Blesa, Rafael;
    • Fortea, Juan;
    • Alcolea, Daniel;
    • Capdevila, Aura;
    • Antonell, Anna;
    • Lladó, Albert;
    • Muñoz-Blanco, José Luís
    Publication type:
    Article
    2
    3

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu017
    Publication type:
    Article
    4

    Genetic comorbidities in Parkinson's disease.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. 831
    By:
    • Nalls, Mike A.;
    • Saad, Mohamad;
    • Noyce, Alastair J.;
    • Keller, Margaux F.;
    • Schrag, Anette;
    • Bestwick, Jonathan P.;
    • Traynor, Bryan J.;
    • Gibbs, J. Raphael;
    • Hernandez, Dena G.;
    • Cookson, Mark R.;
    • Morris, Huw R.;
    • Williams, Nigel;
    • Gasser, Thomas;
    • Heutink, Peter;
    • Wood, Nick;
    • Hardy, John;
    • Martinez, Maria;
    • Singleton, Andrew B.
    Publication type:
    Article
    5
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    Frequent and sex-biased deletion of SLX4IP by illegitimate V(D)J-mediated recombination in childhood acute lymphoblastic leukemia.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. 590, doi. 10.1093/hmg/ddt447
    By:
    • Meissner, Barbara;
    • Bartram, Thies;
    • Eckert, Cornelia;
    • Trka, Jan;
    • Panzer-Grümayer, Renate;
    • Hermanova, Ivana;
    • Ellinghaus, Eva;
    • Franke, Andre;
    • Möricke, Anja;
    • Schrauder, André;
    • Teigler-Schlegel, Andrea;
    • Dörge, Petra;
    • von Stackelberg, Arend;
    • Basso, Giuseppe;
    • Bartram, Claus R.;
    • Kirschner-Schwabe, Renate;
    • Bornhäuser, Beat;
    • Bourquin, Jean-Pierre;
    • Cazzaniga, Giovanni;
    • Hauer, Julia
    Publication type:
    Article
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    12

    Cover Page.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu016
    Publication type:
    Article
    13
    14

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu018
    Publication type:
    Article
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    Overexpression of synphilin-1 promotes clearance of soluble and misfolded alpha-synuclein without restoring the motor phenotype in aged A30P transgenic mice.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. 767, doi. 10.1093/hmg/ddt467
    By:
    • Casadei, Nicolas;
    • Pöhler, Anne-Maria;
    • Tomás-Zapico, Cristina;
    • Torres-Peraza, Jesús;
    • Schwedhelm, Ivo;
    • Witz, Annemarie;
    • Zamolo, Irina;
    • De Heer, Raymond;
    • Spruijt, Berry;
    • Noldus, Lucas P.J.J.;
    • Klucken, Jochen;
    • Lucas, José J.;
    • Kahle, Philipp J.;
    • Krüger, Rejko;
    • Riess, Olaf;
    • Nuber, Silke
    Publication type:
    Article
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    Contents Page.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 3, p. NP, doi. 10.1093/hmg/ddu015
    Publication type:
    Article