Works matching IS 03645134 AND DT 2012 AND VI 71 AND IP 4

Results: 23
    1
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    Reply.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 586, doi. 10.1002/ana.23563
    By:
    • Viswanathan, Anand;
    • Greenberg, Steven M.
    Publication type:
    Article
    4
    5

    Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 520, doi. 10.1002/ana.22685
    By:
    • Friedman, Jennifer;
    • Roze, Emmanuel;
    • Abdenur, Jose E.;
    • Chang, Richard;
    • Gasperini, Serena;
    • Saletti, Veronica;
    • Wali, Gurusidheshwar M.;
    • Eiroa, Hernan;
    • Neville, Brian;
    • Felice, Alex;
    • Parascandalo, Ray;
    • Zafeiriou, Dimitrios I.;
    • Arrabal-Fernandez, Luisa;
    • Dill, Patricia;
    • Eichler, Florian S.;
    • Echenne, Bernard;
    • Gutierrez-Solana, Luis G.;
    • Hoffmann, Georg F.;
    • Hyland, Keith;
    • Kusmierska, Katarzyna
    Publication type:
    Article
    6
    7

    Apping at the Annals.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. A5, doi. 10.1002/ana.23581
    By:
    • Hauser, Stephen L.;
    • Johnston, S. Claiborne
    Publication type:
    Article
    8
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    10

    April 2012.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. A9, doi. 10.1002/ana.23578
    Publication type:
    Article
    11
    12

    A novel X-linked disorder with developmental delay and autistic features.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 498, doi. 10.1002/ana.22673
    By:
    • Kaya, Namik;
    • Colak, Dilek;
    • Albakheet, Albandary;
    • Al-Owain, Mohammad;
    • Abu-Dheim, Nada;
    • Al-Younes, Banan;
    • Al-Zahrani, Jawaher;
    • Mukaddes, Nahit M.;
    • Dervent, Aysin;
    • Al-Dosari, Naji;
    • Al-Odaib, Ali;
    • Kayaalp, Inci V.;
    • Al-Sayed, Moeenaladin;
    • Al-Hassnan, Zuhair;
    • Nester, Michael J.;
    • Al-Dosari, Mohammad;
    • Al-Dhalaan, Hesham;
    • Chedrawi, Aziza;
    • Gunoz, Hulya;
    • Karakas, Bedri
    Publication type:
    Article
    13

    A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 509, doi. 10.1002/ana.22684
    By:
    • Blumen, Sergiu C.;
    • Astord, Stéphanie;
    • Robin, Valérie;
    • Vignaud, Ludivine;
    • Toumi, Nawel;
    • Cieslik, Aurore;
    • Achiron, Anat;
    • Carasso, Ralph L.;
    • Gurevich, Michael;
    • Braverman, Itzhak;
    • Blumen, Nava;
    • Munich, Arnold;
    • Barkats, Martine;
    • Viollet, Louis
    Publication type:
    Article
    14

    NerveCenter: March 2012.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. A5, doi. 10.1002/ana.23580
    By:
    • Stone, Kathlyn
    Publication type:
    Article
    15
    16

    Misfiring in multiple sclerosis.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 437, doi. 10.1002/ana.23537
    By:
    • Craner, Matt J.;
    • Fugger, Lars
    Publication type:
    Article
    17
    18

    Adipocytokines and the risk of ischemic stroke: The PRIME Study.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 478, doi. 10.1002/ana.22669
    By:
    • Prugger, Christof;
    • Luc, Gérald;
    • Haas, Bernadette;
    • Arveiler, Dominique;
    • Machez, Emeline;
    • Ferrieres, Jean;
    • Ruidavets, Jean-Bernard;
    • Bingham, Annie;
    • Montaye, Michèle;
    • Amouyel, Philippe;
    • Yarnell, John;
    • Kee, Frank;
    • Ducimetiere, Pierre;
    • Empana, Jean-Philippe
    Publication type:
    Article
    19
    20

    Mutations in CIZ1 cause adult onset primary cervical dystonia.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 458, doi. 10.1002/ana.23547
    By:
    • Xiao, Jianfeng;
    • Uitti, Ryan J.;
    • Zhao, Yu;
    • Vemula, Satya R.;
    • Perlmutter, Joel S.;
    • Wszolek, Zbigniew K.;
    • Maraganore, Demetrius M.;
    • Auburger, Georg;
    • Leube, Barbara;
    • Lehnhoff, Katja;
    • LeDoux, Mark S.
    Publication type:
    Article
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    FXN methylation predicts expression and clinical outcome in Friedreich ataxia.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 4, p. 487, doi. 10.1002/ana.22671
    By:
    • Evans-Galea, Marguerite V.;
    • Carrodus, Nissa;
    • Rowley, Simone M.;
    • Corben, Louise A.;
    • Tai, Geneieve;
    • Saffery, Richard;
    • Galati, John C.;
    • Wong, Nicholas C.;
    • Craig, Jeffrey M.;
    • Lynch, David R.;
    • Regner, Sean R.;
    • Brocht, Alicia F. D.;
    • Perlman, Susan L.;
    • Bushara, Khalaf O.;
    • Gomez, Christopher M.;
    • Wilmot, George R.;
    • Li, Lingli;
    • Varley, Elizabeth;
    • Delatycki, Martin B.;
    • Sarsero, Joseph P.
    Publication type:
    Article