Found: 3

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  • Exclusion of the DYT1 locus in a non-Jewish family with early-onset dystonia.

    Published in:
    Movement Disorders, 1994, v. 9, n. 6, p. 626, doi. 10.1002/mds.870090608
    By:
    • Bressman, Susan B.;
    • Hunt, Ann L.;
    • Heiman, Gary A.;
    • Brin, Mitchell F.;
    • Burke, Robert E.;
    • Fahn, Stanley;
    • Trugman, Joel M.;
    • de Leon, Deborah;
    • Kramer, Patricia L.;
    • Wilhelmsen, Kirk C.;
    • Nygaard, Torbjoern G.
    Publication type:
    Article

  • Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations.

    Published in:
    Movement Disorders, 2013, v. 28, n. 14, p. 1966, doi. 10.1002/mds.25647
    By:
    • Alcalay, Roy N.;
    • Mirelman, Anat;
    • Saunders‐Pullman, Rachel;
    • Tang, Ming‐X;
    • Mejia Santana, Helen;
    • Raymond, Deborah;
    • Roos, Ernest;
    • Orbe‐Reilly, Martha;
    • Gurevich, Tanya;
    • Bar Shira, Anat;
    • Gana Weisz, Mali;
    • Yasinovsky, Kira;
    • Zalis, Maayan;
    • Thaler, Avner;
    • Deik, Andres;
    • Barrett, Matthew James;
    • Cabassa, Jose;
    • Groves, Mark;
    • Hunt, Ann L.;
    • Lubarr, Naomi
    Publication type:
    Article

  • The pull test: A history.

    Published in:
    Movement Disorders, 2006, v. 21, n. 7, p. 894, doi. 10.1002/mds.20925
    By:
    • Hunt, Ann L.;
    • Sethi, Kapil D.
    Publication type:
    Article