Works matching IS 00139580 AND DT 2009 AND VI 50 AND IP 7


Results: 23
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    SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis.

    Published in:
    Epilepsia (Series 4), 2009, v. 50, n. 7, p. 1670, doi. 10.1111/j.1528-1167.2009.02013.x
    By:
    • Marini, Carla;
    • Scheffer, Ingrid E.;
    • Nabbout, Rima;
    • Mei, Davide;
    • Cox, Kathy;
    • Dibbens, Leanne M.;
    • McMahon, Jacinta M.;
    • Iona, Xenia;
    • Carpintero, Rochio Sanchez;
    • Elia, Maurizio;
    • Cilio, Maria Roberta;
    • Specchio, Nicola;
    • Giordano, Lucio;
    • Striano, Pasquale;
    • Gennaro, Elena;
    • Cross, J. Helen;
    • Kivity, Sara;
    • Neufeld, Miriam Y.;
    • Afawi, Zaid;
    • Andermann, Eva
    Publication type:
    Article
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    Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32.

    Published in:
    Epilepsia (Series 4), 2009, v. 50, n. 7, p. 1679, doi. 10.1111/j.1528-1167.2009.02066.x
    By:
    • Angelicheva, Dora;
    • Tournev, Ivailo;
    • Guergueltcheva, Velina;
    • Mihaylova, Violeta;
    • Azmanov, Dimitar N.;
    • Morar, Bharti;
    • Radionova, Melania;
    • Smith, Shelagh J.;
    • Zlatareva, Dora;
    • Stevens, John M.;
    • Kaneva, Radka;
    • Bojinova, Veneta;
    • Carter, Kim;
    • Brown, Matthew;
    • Jablensky, Assen;
    • Kalaydjieva, Luba;
    • Sander, Josemir W.
    Publication type:
    Article
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    Announcements.

    Published in:
    Epilepsia (Series 4), 2009, v. 50, n. 7, p. 1838, doi. 10.1111/j.1528-1167.2009.02253.x
    Publication type:
    Article