Works matching IS 03645134 AND DT 2017 AND VI 82 AND IP 3


Results: 25
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    Neuromyelitis optica broke my heart too.

    Published in:
    2017
    By:
    • Prin, Pauline;
    • Rodriguez, Yorick;
    • Le Goff, Jean‐Marc;
    • Héroum, Chérif;
    • Molinero, Christelle;
    • Thouvenot, Eric;
    • Le Goff, Jean-Marc;
    • Héroum, Chérif
    Publication type:
    Letter
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    GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.

    Published in:
    2017
    By:
    • Yoo, Yongjin;
    • Jung, Jane;
    • Lee, Yoo‐Na;
    • Lee, Youngha;
    • Cho, Hyosuk;
    • Na, Eunjung;
    • Hong, JeaYeok;
    • Kim, Eunjin;
    • Lee, Jin Sook;
    • Lee, Je Sang;
    • Hong, Chansik;
    • Park, Sang‐Yoon;
    • Wie, Jinhong;
    • Miller, Kathryn;
    • Shur, Natasha;
    • Clow, Cheryl;
    • Ebel, Roseànne S.;
    • DeBrosse, Suzanne D.;
    • Henderson, Lindsay B.;
    • Willaert, Rebecca
    Publication type:
    journal article
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    Polygenic hazard scores in preclinical Alzheimer disease.

    Published in:
    2017
    By:
    • Tan, Chin Hong;
    • Hyman, Bradley T.;
    • Tan, Jacinth J. X.;
    • Hess, Christopher P.;
    • Dillon, William P.;
    • Schellenberg, Gerard D.;
    • Besser, Lilah M.;
    • Kukull, Walter A.;
    • Kauppi, Karolina;
    • McEvoy, Linda K.;
    • Andreassen, Ole A.;
    • Dale, Anders M.;
    • Fan, Chun Chieh;
    • Desikan, Rahul S.
    Publication type:
    journal article
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    Natural history of Charcot-Marie-Tooth disease during childhood.

    Published in:
    2017
    By:
    • Cornett, Kayla M.D.;
    • Menezes, Manoj P.;
    • Shy, Rosemary R.;
    • Moroni, Isabella;
    • Pagliano, Emanuela;
    • Pareyson, Davide;
    • Estilow, Timothy;
    • Yum, Sabrina W.;
    • Bhandari, Trupti;
    • Muntoni, Francesco;
    • Laura, Matilde;
    • Reilly, Mary M.;
    • Finkel, Richard S.;
    • Eichinger, Kate J.;
    • Herrmann, David N.;
    • Bray, Paula;
    • Halaki, Mark;
    • Shy, Michael E.;
    • Burns, Joshua;
    • Cornett, Kayla MD
    Publication type:
    journal article
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    Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors.

    Published in:
    2017
    By:
    • Ortigoza‐Escobar, Juan Darío;
    • Alfadhel, Majid;
    • Molero‐Luis, Marta;
    • Darin, Niklas;
    • Spiegel, Ronen;
    • de Coo, Irenaeus F.;
    • Gerards, Mike;
    • Taylor, Robert W.;
    • Artuch, Rafael;
    • Nashabat, Marwan;
    • Rodríguez‐Pombo, Pilar;
    • Tabarki, Brahim;
    • Pérez‐Dueñas, Belén;
    • Distelmaier, Felix;
    • Hahn, Andreas;
    • Morava, Eva;
    • Banka, Siddharth;
    • Debs, Rabab;
    • Fraser, Jamie L.;
    • Isohanni, Pirjo
    Publication type:
    journal article
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    Issue Information - TOC.

    Published in:
    Annals of Neurology, 2017, v. 82, n. 3, p. n/a, doi. 10.1002/ana.25043
    Publication type:
    Article