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Number of items: 3.

von Spiczak, Sarah and Lal, D. and Reinthaler, E. M. and Steiner, I. and Nothnagel, M. and Laube, Bodo and Schwake, M. and Hoffmann, P. and Herms, S. and Altmüller, J. and Toliat, M. R. and Thiele, H. and Nürnberg, P. and Wilhelm, C. and Stephani, U. and Helbig, I. and Lerche, H. and Zimprich, F. and Neubauer, B. A. and Biskup, S. and Lemke, J. R. (2013):
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
In: Epilepsia, 54p. 344, ISSN 0013-9580,

Lemke, Johannes R. and Lal, Dennis and Reinthaler, Eva M. and Steiner, Isabelle and Nothnagel, Michael and Alber, Michael and Geider, Kirsten and Laube, Bodo and Schwake, Michael and Finsterwalder, Katrin and Franke, Andre and Schilhabel, Markus and Jähn, Johanna A. and Muhle, Hiltrud and Boor, Rainer and Van Paesschen, Wim and Caraballo, Roberto and Fejerman, Natalio and Weckhuysen, Sarah and De Jonghe, Peter and Larsen, Jan and Møller, Rikke S. and Hjalgrim, Helle and Addis, Laura and Tang, Shan and Hughes, Elaine and Pal, Deb K. and Veri, Kadi and Vaher, Ulvi and Talvik, Tiina and Dimova, Petia and Guerrero López, Rosa and Serratosa, José M. and Linnankivi, Tarja and Lehesjoki, Anna-Elina and Ruf, Susanne and Wolff, Markus and Buerki, Sarah and Wohlrab, Gabriele and Kroell, Judith and Datta, Alexandre N. and Fiedler, Barbara and Kurlemann, Gerhard and Kluger, Gerhard and Hahn, Andreas and Haberlandt, D. Edda and Kutzer, Christina and Sperner, Jürgen and Becker, Felicitas and Weber, Yvonne G. and Feucht, Martha and Steinböck, Hannelore and Neophythou, Birgit and Ronen, Gabriel M. and Gruber-Sedlmayr, Ursula and Geldner, Julia and Harvey, Robert J. and Hoffmann, Per and Herms, Stefan and Altmüller, Janine and Toliat, Mohammad R. and Thiele, Holger and Nürnberg, Peter and Wilhelm, Christian and Stephani, Ulrich and Helbig, Ingo and Lerche, Holger and Zimprich, Fritz and Neubauer, Bernd A. and Biskup, Saskia and von Spiczak, Sarah (2013):
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
In: Nature genetics, 45 (9), pp. 1067-72, ISSN 1546-1718,

Endele, Sabine and Rosenberger, Georg and Geider, Kirsten and Popp, Bernt and Tamer, Ceyhun and Stefanova, Irina and Milh, Mathieu and Kortüm, Fanny and Fritsch, Angela and Pientka, Friederike K. and Hellenbroich, Yorck and Kalscheuer, Vera M. and Kohlhase, Jürgen and Moog, Ute and Rappold, Gudrun and Rauch, Anita and Ropers, Hans-Hilger and von Spiczak, Sarah and Tönnies, Holger and Villeneuve, Nathalie and Villard, Laurent and Zabel, Bernhard and Zenker, Martin and Laube, Bodo and Reis, André and Wieczorek, Dagmar and Van Maldergem, Lionel and Kutsche, Kerstin (2010):
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
In: Nature genetics, 42 (11), pp. 1021-6, ISSN 1546-1718,

This list was generated on Tue Jun 2 01:13:30 2020 CEST.