Works matching IS 00139580 AND DT 2014 AND VI 55 AND IP 7


Results: 28
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    Co-occurring malformations of cortical development and SCN1A gene mutations.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 7, p. 1009, doi. 10.1111/epi.12658
    By:
    • Barba, Carmen;
    • Parrini, Elena;
    • Coras, Roland;
    • Galuppi, Anna;
    • Craiu, Dana;
    • Kluger, Gerhard;
    • Parmeggiani, Antonia;
    • Pieper, Tom;
    • Schmitt‐Mechelke, Thomas;
    • Striano, Pasquale;
    • Giordano, Flavio;
    • Blumcke, Ingmar;
    • Guerrini, Renzo
    Publication type:
    Article
    21

    My epilepsy story- PCDH19 Alliance.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 7, p. 968, doi. 10.1111/epi.12555
    By:
    • Walters, Julie;
    • Wells‐Kilpatrick, Karin;
    • Pandeleos, Trista
    Publication type:
    Article
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    Early onset epileptic encephalopathy caused by de novo SCN8A mutations.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 7, p. 994, doi. 10.1111/epi.12668
    By:
    • Ohba, Chihiro;
    • Kato, Mitsuhiro;
    • Takahashi, Satoru;
    • Lerman‐Sagie, Tally;
    • Lev, Dorit;
    • Terashima, Hiroshi;
    • Kubota, Masaya;
    • Kawawaki, Hisashi;
    • Matsufuji, Mayumi;
    • Kojima, Yasuko;
    • Tateno, Akihiko;
    • Goldberg‐Stern, Hadassa;
    • Straussberg, Rachel;
    • Marom, Dafna;
    • Leshinsky‐Silver, Esther;
    • Nakashima, Mitsuko;
    • Nishiyama, Kiyomi;
    • Tsurusaki, Yoshinori;
    • Miyake, Noriko;
    • Tanaka, Fumiaki
    Publication type:
    Article
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    Announcements.

    Published in:
    Epilepsia (Series 4), 2014, v. 55, n. 7, p. 1135, doi. 10.1111/epi.12363
    Publication type:
    Article
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