Works matching IS 00068950 AND DT 2010 AND VI 133 AND IP 3


Results: 33
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    Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 655, doi. 10.1093/brain/awp336
    By:
    • Leen, Wilhelmina G.;
    • Klepper, Joerg;
    • Verbeek, Marcel M.;
    • Leferink, Maike;
    • Hofste, Tom;
    • van Engelen, Baziel G.;
    • Wevers, Ron A.;
    • Arthur, Todd;
    • Bahi-Buisson, Nadia;
    • Ballhausen, Diana;
    • Bekhof, Jolita;
    • van Bogaert, Patrick;
    • Carrilho, Inês;
    • Chabrol, Brigitte;
    • Champion, Michael P.;
    • Coldwell, James;
    • Clayton, Peter;
    • Donner, Elizabeth;
    • Evangeliou, Athanasios;
    • Ebinger, Friedrich
    Publication type:
    Article
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    DJ-1 and α-synuclein in human cerebrospinal fluid as biomarkers of Parkinson’s disease.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 713, doi. 10.1093/brain/awq008
    By:
    • Zhen Hong;
    • Min Shi;
    • Chung, Kathryn A.;
    • Quinn, Joseph F.;
    • Peskind, Elaine R.;
    • Galasko, Douglas;
    • Jankovic, Joseph;
    • Zabetian, Cyrus P.;
    • Leverenz, James B.;
    • Baird, Geoffrey;
    • Montine, Thomas J.;
    • Hancock, Aneeka M.;
    • Hyejin Hwang;
    • Pan, Catherine;
    • Bradner, Joshua;
    • Kang, Un J.;
    • Jensen, Poul H.;
    • Jing Zhang
    Publication type:
    Article
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    ‘Looks like epilepsy to me!’.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 651, doi. 10.1093/brain/awq038
    By:
    • Warlow, Charles
    Publication type:
    Article
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    Life without a cerebellum.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 652, doi. 10.1093/brain/awq030
    By:
    • Lemon, R. N.;
    • Edgley, S. A.
    Publication type:
    Article
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    Cerebellar agenesis revisited.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 941, doi. 10.1093/brain/awp265
    By:
    • Boyd, C. A. R.
    Publication type:
    Article
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    Mitochondrial DNA mutations affect calcium handling in differentiated neurons.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 787, doi. 10.1093/brain/awq023
    By:
    • Trevelyan, Andrew J.;
    • Kirby, Denise M.;
    • Smulders-Srinivasan, Tora K.;
    • Nooteboom, Marco;
    • Acin-Perez, Rebeca;
    • Enriquez, José Antonio;
    • Whittington, Miles A.;
    • Lightowlers, Robert N.;
    • Turnbull, Doug M.
    Publication type:
    Article
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    Editorial.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 643, doi. 10.1093/brain/awq036
    By:
    • Compston, Alastair
    Publication type:
    Article
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    Multi-system neurological disease is common in patients with OPA1 mutations.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 771, doi. 10.1093/brain/awq007
    By:
    • Yu-Wai-Man, P.;
    • Griffiths, P. G.;
    • Gorman, G. S.;
    • Lourenco, C. M.;
    • Wright, A. F.;
    • Auer-Grumbach, M.;
    • Toscano, A.;
    • Musumeci, O.;
    • Valentino, M. L.;
    • Caporali, L.;
    • Lamperti, C.;
    • Tallaksen, C. M.;
    • Duffey, P.;
    • Miller, J.;
    • Whittaker, R. G.;
    • Baker, M. R.;
    • Jackson, M. J.;
    • Clarke, M. P.;
    • Dhillon, B.;
    • Czermin, B.
    Publication type:
    Article
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    Attenuated variants of Lesch-Nyhan disease.

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 671, doi. 10.1093/brain/awq013
    By:
    • Jinnah, H. A.;
    • Ceballos-Picot, Irene;
    • Torres, Rosa J.;
    • Visser, Jasper E.;
    • Schretlen, David J.;
    • Verdu, Alfonso;
    • Laróvere, Laura E.;
    • Chung-Jen Chen;
    • Cossu, Antonello;
    • Chien-Hui Wu;
    • Sampat, Radhika;
    • Shun-Jen Chang;
    • de Kremer, Raquel Dodelson;
    • Nyhan, William;
    • Harris, James C.;
    • Reich, Stephen G.;
    • Puig, Juan G.
    Publication type:
    Article