Works matching IS 08853185 AND DT 2013 AND VI 28 AND IP 2


Results: 41
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    De novo FTL mutation: A clinical, neuroimaging, and molecular study.

    Published in:
    Movement Disorders, 2013, v. 28, n. 2, p. 252, doi. 10.1002/mds.25275
    By:
    • Storti, Eugenia;
    • Cortese, Francesca;
    • Fabio, Roberto;
    • Fiorillo, Chiara;
    • Pierallini, Alberto;
    • Tessa, Alessandra;
    • Valleriani, Annamaria;
    • Pierelli, Francesco;
    • Santorelli, Filippo M.;
    • Casali, Carlo
    Publication type:
    Article
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    Common data elements for clinical research in Friedreich's ataxia.

    Published in:
    Movement Disorders, 2013, v. 28, n. 2, p. 190, doi. 10.1002/mds.25201
    By:
    • Lynch, David R.;
    • Pandolfo, Massimo;
    • Schulz, Jorg B.;
    • Perlman, Susan;
    • Delatycki, Martin B.;
    • Payne, R. Mark;
    • Shaddy, Robert;
    • Fischbeck, Kenneth H.;
    • Farmer, Jennifer;
    • Kantor, Paul;
    • Raman, Subha V.;
    • Hunegs, Lisa;
    • Odenkirchen, Joanne;
    • Miller, Kristy;
    • Kaufmann, Petra
    Publication type:
    Article
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    Diabetes and risk of Parkinson's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 2, p. 257, doi. 10.1002/mds.25211
    By:
    • Cereda, Emanuele;
    • Barichella, Michela;
    • Pedrolli, Carlo;
    • Klersy, Catherine;
    • Cassani, Erica;
    • Caccialanza, Riccardo;
    • Pezzoli, Gianni
    Publication type:
    Article
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    Enlarged hyperechogenic substantia nigra as a risk marker for Parkinson's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 2, p. 216, doi. 10.1002/mds.25192
    By:
    • Berg, Daniela;
    • Behnke, Stefanie;
    • Seppi, Klaus;
    • Godau, Jana;
    • Lerche, Stefanie;
    • Mahlknecht, Philipp;
    • Liepelt‐Scarfone, Inga;
    • Pausch, Christoph;
    • Schneider, Niko;
    • Gaenslen, Alexandra;
    • Brockmann, Kathrin;
    • Srulijes, Karin;
    • Huber, Heiko;
    • Wurster, Isabel;
    • Stockner, Heike;
    • Kiechl, Stefan;
    • Willeit, Johann;
    • Gasperi, Arno;
    • Fassbender, Klaus;
    • Gasser, Thomas
    Publication type:
    Article
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    The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.

    Published in:
    Movement Disorders, 2013, v. 28, n. 2, p. 232, doi. 10.1002/mds.25248
    By:
    • Duran, Raquel;
    • Mencacci, Niccolo E.;
    • Angeli, Aikaterini V.;
    • Shoai, Maryam;
    • Deas, Emma;
    • Houlden, Henry;
    • Mehta, Atul;
    • Hughes, Derralynn;
    • Cox, Timothy M.;
    • Deegan, Patrick;
    • Schapira, Anthony H.;
    • Lees, Andrew J.;
    • Limousin, Patricia;
    • Jarman, Paul R.;
    • Bhatia, Kailash P.;
    • Wood, Nicholas W.;
    • Hardy, John;
    • Foltynie, Tom
    Publication type:
    Article
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