Works matching IS 08853185 AND DT 2008 AND VI 23 AND IP 10


Results: 30
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    Familial Parkinsonism with digenic parkin and PINK1 mutations.

    Published in:
    Movement Disorders, 2008, v. 23, n. 10, p. 1461, doi. 10.1002/mds.22143
    By:
    • Funayama, Manabu;
    • Li, Yuanzhe;
    • Tsoi, Tak-Hong;
    • Lam, Ching-Wan;
    • Ohi, Takekazu;
    • Yazawa, Shogo;
    • Uyama, Eiichiro;
    • Djaldetti, Ruth;
    • Melamed, Eldad;
    • Yoshino, Hiroyo;
    • Imamichi, Yoko;
    • Takashima, Hiroshi;
    • Nishioka, Kenya;
    • Sato, Kenichi;
    • Tomiyama, Hiroyuki;
    • Kubo, Shin-Ichiro;
    • Mizuno, Yoshikuni;
    • Hattori, Nobutaka
    Publication type:
    Article
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    Cerebellar ataxia as a possible organ-specific autoimmune disease.

    Published in:
    Movement Disorders, 2008, v. 23, n. 10, p. 1370, doi. 10.1002/mds.22129
    By:
    • Hadjivassiliou, Marios;
    • Boscolo, Sabrina;
    • Tongiorgi, Enrico;
    • Grünewald, Richard A.;
    • Sharrack, Basil;
    • Sanders, David S.;
    • Woodroofe, Nicola;
    • Davies-Jones, G. Aelwyn B.
    Publication type:
    Article
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    Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type.

    Published in:
    Movement Disorders, 2008, v. 23, n. 10, p. 1384, doi. 10.1002/mds.22115
    By:
    • Temudo, Teresa;
    • Ramos, Elisabete;
    • Dias, Karin;
    • Barbot, Clara;
    • Vieira, Jose P.;
    • Moreira, Ana;
    • Calado, Eulalia;
    • Carrilho, Ines;
    • Oliveira, Guiomar;
    • Levy, Antonio;
    • Fonseca, Maria;
    • Cabral, Alexandra;
    • Cabral, Pedro;
    • Monteiro, Joao P;
    • Borges, Luis;
    • Gomes, Roseli;
    • Santos, Manuela;
    • Sequeiros, Jorge;
    • Maciel, Patricia
    Publication type:
    Article
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