Works matching IS 00068950 AND DT 2016 AND VI 139 AND IP 4


Results: 35
    1

    Corrigendum.

    Published in:
    2016
    Publication type:
    corrected article
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    Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

    Published in:
    2016
    By:
    • Bannwarth, Sylvie;
    • Ait-El-Mkadem, Samira;
    • Chaussenot, Annabelle;
    • Genin, Emmanuelle C.;
    • Lacas-Gervais, Sandra;
    • Fragaki, Konstantina;
    • Berg-Alonso, Laetitia;
    • Kageyama, Yusuke;
    • Serre, Valérie;
    • Moore, David;
    • Verschueren, Annie;
    • Rouzier, Cécile;
    • Ber, Isabelle Le;
    • Augé, Gaëlle;
    • Cochaud, Charlotte;
    • Lespinasse, Françoise;
    • N'Guyen, Karine;
    • de Septenville, Anne;
    • Brice, Alexis;
    • Yu-Wai-Man, Patrick
    Publication type:
    Letter
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    White matter hyperintensities and imaging patterns of brain ageing in the general population.

    Published in:
    2016
    By:
    • Habes, Mohamad;
    • Erus, Guray;
    • Toledo, Jon B.;
    • Tianhao Zhang;
    • Bryan, Nick;
    • Launer, Lenore J.;
    • Rosseel, Yves;
    • Janowitz, Deborah;
    • Doshi, Jimit;
    • Van der Auwera, Sandra;
    • von Sarnowski, Bettina;
    • Hegenscheid, Katrin;
    • Hosten, Norbert;
    • Homuth, Georg;
    • Völzke, Henry;
    • Schminke, Ulf;
    • Hoffmann, Wolfgang;
    • Grabe, Hans J.;
    • Davatzikos, Christos;
    • Zhang, Tianhao
    Publication type:
    journal article
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    Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis.

    Published in:
    2016
    By:
    • Vercruysse, Pauline;
    • Sinniger, Jérôme;
    • Oussini, Hajer El;
    • Scekic-Zahirovic, Jelena;
    • Dieterlé, Stéphane;
    • Dengler, Reinhard;
    • Meyer, Thomas;
    • Zierz, Stephan;
    • Kassubek, Jan;
    • Fischer, Wilhelm;
    • Dreyhaupt, Jens;
    • Grehl, Torsten;
    • Hermann, Andreas;
    • Grosskreutz, Julian;
    • Witting, Anke;
    • Den Bosch, Ludo Van;
    • Spreux-Varoquaux, Odile;
    • El Oussini, Hajer;
    • Van Den Bosch, Ludo;
    • GERP ALS Study Group
    Publication type:
    journal article
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    CCDC88A mutations cause PEHO-like syndrome in humans and mouse.

    Published in:
    2016
    By:
    • Nahorski, Michael S.;
    • Asai, Masato;
    • Wakeling, Emma;
    • Parker, Alasdair;
    • Asai, Naoya;
    • Canham, Natalie;
    • Holder, Susan E.;
    • Ya-Chun Chen;
    • Dyer, Joshua;
    • Brady, Angela F.;
    • Masahide Takahashi;
    • Woods, C. Geoffrey;
    • Chen, Ya-Chun;
    • Takahashi, Masahide
    Publication type:
    journal article
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