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  • Reply.

    Published in:
    2016
    By:
    • Gardella, Elena;
    • Beniczky, Sándor;
    • Møller, Rikke S.;
    • Becker, Felicitas;
    • Lemke, Johannes R.;
    • Syrbe, Steffen;
    • Eiberg, Hans;
    • Bast, Thomas;
    • Steinhoff, Bernhard;
    • Nürnberg, Peter;
    • Gellert, Pia;
    • Dahl, Hans Atli;
    • Weckhuysen, Sarah;
    • Heron, Sarah E.;
    • Dibbens, Leanne M.;
    • Hjalgrim, Helle;
    • Lerche, Holger;
    • Weber, Yvonne G.;
    • Beniczky, Sándor;
    • Møller, Rikke S
    Publication type:
    Letter

  • Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation.

    Published in:
    2016
    By:
    • Gardella, Elena;
    • Becker, Felicitas;
    • Møller, Rikke S.;
    • Schubert, Julian;
    • Lemke, Johannes R.;
    • Larsen, Line H. G.;
    • Eiberg, Hans;
    • Nothnagel, Michael;
    • Thiele, Holger;
    • Altmüller, Janine;
    • Syrbe, Steffen;
    • Merkenschlager, Andreas;
    • Bast, Thomas;
    • Steinhoff, Bernhard;
    • Nürnberg, Peter;
    • Mang, Yuan;
    • Bakke Møller, Louise;
    • Gellert, Pia;
    • Heron, Sarah E.;
    • Dibbens, Leanne M.
    Publication type:
    journal article

  • Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies.

    Published in:
    Molecular Syndromology, 2016, v. 7, n. 4, p. 210, doi. 10.1159/000448369
    By:
    • Møller, Rikke S.;
    • Larsen, Line H. G.;
    • Johannesen, Katrine M.;
    • Talvik, Inga;
    • Talvik, Tiina;
    • Vaher, Ulvi;
    • Miranda, Maria J.;
    • Farooq, Muhammad;
    • Nielsen, Jens E. K.;
    • Svendsen, Lene Lavard;
    • Kjelgaard, Ditte B.;
    • Linnet, Karen M.;
    • Qin Hao;
    • Uldall, Peter;
    • Frangu, Mimoza;
    • Tommerup, Niels;
    • Baig, Shahid M.;
    • Abdullah, Uzma;
    • Born, Alfred P.;
    • Gellert, Pia
    Publication type:
    Article