Works matching IS 00139580 AND DT 2013 AND VI 54 AND IP 7

Results: 24
    1

    Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1282, doi. 10.1111/epi.12200
    By:
    • Kato, Mitsuhiro;
    • Yamagata, Takanori;
    • Kubota, Masaya;
    • Arai, Hiroshi;
    • Yamashita, Sumimasa;
    • Nakagawa, Taku;
    • FujII, Takanari;
    • Sugai, Kenji;
    • Imai, Kaoru;
    • Uster, Tami;
    • Chitayat, David;
    • Weiss, Shelly;
    • Kashii, Hirofumi;
    • Kusano, Ryosuke;
    • Matsumoto, Ayumi;
    • Nakamura, Kazuyuki;
    • Oyazato, Yoshinobu;
    • Maeno, Mari;
    • Nishiyama, Kiyomi;
    • Kodera, Hirofumi
    Publication type:
    Article
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    Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1262, doi. 10.1111/epi.12203
    By:
    • Kodera, Hirofumi;
    • Kato, Mitsuhiro;
    • Nord, Alex S.;
    • Walsh, Tom;
    • Lee, Ming;
    • Yamanaka, Gaku;
    • Tohyama, Jun;
    • Nakamura, Kazuyuki;
    • Nakagawa, Eiji;
    • Ikeda, Tae;
    • Ben ‐ Zeev, Bruria;
    • Lev, Dorit;
    • Lerman ‐ Sagie, Tally;
    • Straussberg, Rachel;
    • Tanabe, Saori;
    • Ueda, Kazutoshi;
    • Amamoto, Masano;
    • Ohta, Sayaka;
    • Nonoda, Yutaka;
    • Nishiyama, Kiyomi
    Publication type:
    Article
    8

    Erratum.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1333, doi. 10.1111/epi.12317
    Publication type:
    Article
    9
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    International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1315, doi. 10.1111/epi.12220
    By:
    • Blümcke, Ingmar;
    • Thom, Maria;
    • Aronica, Eleonora;
    • Armstrong, Dawna D.;
    • Bartolomei, Fabrice;
    • Bernasconi, Andrea;
    • Bernasconi, Neda;
    • Bien, Christian G.;
    • Cendes, Fernando;
    • Coras, Roland;
    • Cross, J. Helen;
    • Jacques, Thomas S.;
    • Kahane, Philippe;
    • Mathern, Gary W.;
    • Miyata, Haijme;
    • Moshé, Solomon L.;
    • Oz, Buge;
    • Özkara, Çiğdem;
    • Perucca, Emilio;
    • Sisodiya, Sanjay
    Publication type:
    Article
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    Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1288, doi. 10.1111/epi.12194
    By:
    • Michelucci, Roberto;
    • Pasini, Elena;
    • Malacrida, Sandro;
    • Striano, Pasquale;
    • Bonaventura, Carlo Di;
    • Pulitano, Patrizia;
    • Bisulli, Francesca;
    • Egeo, Gabriella;
    • Santulli, Lia;
    • Sofia, Vito;
    • Gambardella, Antonio;
    • Elia, Maurizio;
    • Falco, Arturo;
    • Neve, Angela la;
    • Banfi, Paola;
    • Coppola, Giangennaro;
    • Avoni, Patrizia;
    • Binelli, Simona;
    • Boniver, Clementina;
    • Pisano, Tiziana
    Publication type:
    Article
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    Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1270, doi. 10.1111/epi.12201
    By:
    • Veeramah, Krishna R.;
    • Johnstone, Laurel;
    • Karafet, Tatiana M.;
    • Wolf, Daniel;
    • Sprissler, Ryan;
    • Salogiannis, John;
    • Barth ‐ Maron, Asa;
    • Greenberg, Michael E.;
    • Stuhlmann, Till;
    • Weinert, Stefanie;
    • Jentsch, Thomas J.;
    • Pazzi, Marjorie;
    • Restifo, Linda L.;
    • Talwar, Dinesh;
    • Erickson, Robert P.;
    • Hammer, Michael F.
    Publication type:
    Article
    18

    Announcements.

    Published in:
    Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1332, doi. 10.1111/epi.12315
    Publication type:
    Article
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