Works matching IS 03645134 AND DT 2008 AND VI 63 AND IP 6

Results: 19
    1
    2

    Genomic investigation of α-synuclein multiplication and parkinsonism.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 743, doi. 10.1002/ana.21380
    By:
    • Ross, Owen A.;
    • Braithwaite, Adam T.;
    • Skipper, Lisa M.;
    • Kachergus, Jennifer;
    • Hulihan, Mary M.;
    • Middleton, Frank A.;
    • Nishioka, Kenya;
    • Fuchs, Julia;
    • Gasser, Thomas;
    • Maraganore, Demetrius M.;
    • Adler, Charles H.;
    • Larvor, Lydie;
    • Chartier-Harlin, Marie-Christine;
    • Nilsson, Christer;
    • Langston, J. William;
    • Gwinn, Katrina;
    • Hattori, Nobutaka;
    • Farrer, Matthew J.
    Publication type:
    Article
    3
    4

    A new prionopathy.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 677, doi. 10.1002/ana.21447
    By:
    • Will, Robert;
    • Head, Mark
    Publication type:
    Article
    5
    6
    7

    A novel human disease with abnormal prion protein sensitive to protease.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 697, doi. 10.1002/ana.21420
    By:
    • Gambetti, Pierluigi;
    • Dong, Zhiqian;
    • Yuan, Jue;
    • Xiao, Xiangzhu;
    • Zheng, Mengjie;
    • Alshekhlee, Amer;
    • Castellani, Rudy;
    • Cohen, Mark;
    • Barria, Marcelo A.;
    • Gonzalez-Romero, D.;
    • Belay, Ermias D.;
    • Schonberger, Lawrence B.;
    • Marder, Karen;
    • Harris, Carrie;
    • Burke, James R.;
    • Montine, Thomas;
    • Wisniewski, Thomas;
    • Dickson, Dennis W.;
    • Soto, Claudio;
    • Hulette, Christine M.
    Publication type:
    Article
    8

    That vexing problem of compensation.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. A11, doi. 10.1002/ana.21431
    By:
    • Hauser, Stephen L.;
    • Johnston, S. Claiborne
    Publication type:
    Article
    9
    10

    Treatment of childhood arterial ischemic stroke.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 679, doi. 10.1002/ana.21406
    By:
    • Bernard, Timothy J.;
    • Goldenberg, Neil A.;
    • Armstrong-Wells, Jennifer;
    • Amlie-Lefond, Catherine;
    • Fullerton, Heather J.
    Publication type:
    Article
    11
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    15
    16

    Hereditary optic neuropathies share a common mitochondrial coupling defect.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 794, doi. 10.1002/ana.21385
    By:
    • Chevrollier, Arnaud;
    • Guillet, Virginie;
    • Loiseau, Dominique;
    • Gueguen, Naïg;
    • Pou de Crescenzo, Marie-Anne;
    • Verny, Christophe;
    • Ferre, Marc;
    • Dollfus, Hélène;
    • Odent, Sylvie;
    • Milea, Dan;
    • Goizet, Cyril;
    • Amati-Bonneau, Patrizia;
    • Procaccio, Vincent;
    • Bonneau, Dominique;
    • Reynier, Pascal
    Publication type:
    Article
    17

    Erratum.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 803, doi. 10.1002/ana.21441
    Publication type:
    Article
    18
    19

    Predicting progression in primary progressive multiple sclerosis: A 10-year multicenter study.

    Published in:
    Annals of Neurology, 2008, v. 63, n. 6, p. 790, doi. 10.1002/ana.21375
    By:
    • Khaleeli, Zhaleh;
    • Ciccarelli, Olga;
    • Manfredonia, Francesco;
    • Barkhof, Frederik;
    • Brochet, Bruno;
    • Cercignani, Mara;
    • Dousset, Vincent;
    • Filippi, Massimo;
    • Montalban, Xavier;
    • Polman, Chris;
    • Rovaris, Marco;
    • Rovira, Alex;
    • Sastre-Garriga, Jaume;
    • Vellinga, Machteld;
    • Miller, David;
    • Thompson, Alan
    Publication type:
    Article