Works matching IS 08853185 AND DT 2018 AND VI 33


Results: 413
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    A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.

    Published in:
    2018
    By:
    • Salpietro, Vincenzo;
    • Perez‐Dueñas, Belen;
    • Nakashima, Kosuke;
    • San Antonio‐Arce, Victoria;
    • Manole, Andreea;
    • Efthymiou, Stephanie;
    • Vandrovcova, Jana;
    • Bettencourt, Conceicao;
    • Mencacci, Niccolò E.;
    • Klein, Christine;
    • Kelly, Michy P.;
    • Davies, Ceri H.;
    • Kimura, Haruhide;
    • Macaya, Alfons;
    • Houlden, Henry;
    • Perez-Dueñas, Belen;
    • San Antonio-Arce, Victoria
    Publication type:
    journal article
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    Nonmotor symptoms evolution during 24 months of bilateral subthalamic stimulation in Parkinson's disease.

    Published in:
    2018
    By:
    • Dafsari, Haidar S.;
    • Silverdale, Monty;
    • Strack, Marian;
    • Rizos, Alexandra;
    • Ashkan, Keyoumars;
    • Mahlstedt, Picabo;
    • Sachse, Lena;
    • Steffen, Julia;
    • Dembek, Till A.;
    • Visser‐Vandewalle, Veerle;
    • Evans, Julian;
    • Antonini, Angelo;
    • Martinez‐Martin, Pablo;
    • Ray‐Chaudhuri, K.;
    • Timmermann, Lars;
    • on behalf of EUROPAR and the IPMDS Non Motor PD Study Group;
    • Visser-Vandewalle, Veerle;
    • Martinez-Martin, Pablo;
    • Ray-Chaudhuri, K;
    • EUROPAR and the IPMDS Non Motor PD Study Group
    Publication type:
    journal article
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    C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias.

    Published in:
    2018
    By:
    • Figueroa, Karla P.;
    • Gan, Shi‐Rui;
    • Perlman, Susan;
    • Wilmot, George;
    • Gomez, Christopher M.;
    • Schmahmann, Jeremy;
    • Paulson, Henry;
    • Shakkottai, Vikram G.;
    • Ying, Sarah H.;
    • Zesiewicz, Theresa;
    • Bushara, Khalaf;
    • Geschwind, Michael;
    • Xia, Guangbin;
    • Subramony, S. H.;
    • Ashizawa, Tetsuo;
    • Pulst, Stefan M.;
    • Kuo, Sheng‐Han;
    • Gan, Shi-Rui;
    • Kuo, Sheng-Han
    Publication type:
    Letter
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    Issue Information.

    Published in:
    Movement Disorders, 2018, v. 33, n. 3, p. 1, doi. 10.1002/mds.27150
    Publication type:
    Article
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