未登录Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes
Lemke, Johannes R.; Lal, Dennis; Reinthaler, Eva M.; Steiner, Isabelle; Nothnagel, Michael; Alber, Michael; Geider, Kirsten; Laube, Bodo; Schwake, Michael; Finsterwalder, Katrin; Franke, Andre; Schilhabel, Markus; Jaehn, Johanna A.; Muhle, Hiltrud; Boor, Rainer; Van Paesschen, Wim; Caraballo, Roberto; Fejerman, Natalio; Weckhuysen, Sarah; De Jonghe, Peter; Larsen, Jan; Moller, Rikke S.; Hjalgrim, Helle; Addis, Laura; Tang, Shan; Hughes, Elaine; Pal, Deb K.; Veri, Kadi; Vaher, Ulvi; Talvik, Tiina; Dimova, Petia; Lopez, Rosa Guerrero; Serratosa, Jose M.; Linnankivi, Tarja; Lehesjoki, Anna-Elina; Ruf, Susanne; Wolff, Markus; Buerki, Sarah; Wohlrab, Gabriele; Kroell, Judith; Datta, Alexandre N.; Fiedler, Barbara; Kurlemann, Gerhard; Kluger, Gerhard; Hahn, Andreas; Haberlandt, D. Edda; Kutzer, Christina; Sperner, Juergen; Becker, Felicitas; Weber, Yvonne G.; Feucht, Martha; Steinboeck, Hannelore; Neophythou, Birgit; Ronen, Gabriel M.; Gruber-Sedlmayr, Ursula; Geldner, Julia; Harvey, Robert J.; Hoffmann, Per; Herms, Stefan; Altmueller, Janine; Toliat, Mohammad R.; Thiele, Holger; Nuernberg, Peter; Wilhelm, Christian; Stephani, Ulrich; Helbig, Ingo; Lerche, Holger; Zimprich, Fritz; Neubauer, Bernd A.; Biskup, Saskia; von Spiczak, Sarah .png)
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收藏PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraineCloarec, Robin; Bruneau, Nadine; Rudolf, Gabrielle; Massacrier, Annick; Salmi, Manal; Bataillard, Marc; Boulay, Clotilde; Caraballo, Roberto; Fejerman, Natalio; Genton, Pierre; Hirsch, Edouard; Hunter, Alasdair; Lesca, Gaetan; Motte, Jacques; Roubertie, Agathe; Sanlaville, Damien; Wong, Sau-Wei; Fu, Ying-Hui; Rochette, Jacques; Ptacek, Louis J.; Szepetowski, Pierre 分享 收藏 分享 收藏 Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile ConvulsionsLee, Hsien-Yang; Huang, Yong; Bruneau, Nadine; Roll, Patrice; Roberson, Elisha D. O.; Hermann, Mark; Quinn, Emily; Maas, James; Edwards, Robert; Ashizawa, Tetsuo; Baykan, Betul; Bhatia, Kailash; Bressman, Susan; Bruno, Michiko K.; Brunt, Ewout R.; Caraballo, Roberto; Echenne, Bernard; Fejerman, Natalio; Frucht, Steve; Gurnett, Christina A.; Hirsch, Edouard; Houlden, Henry; Jankovic, Joseph; Lee, Wei-Ling; Lynch, David R.; Mohammed, Shehla; Mueller, Ulrich; Nespeca, Mark P.; Renner, David; Rochette, Jacques; Rudolf, Gabrielle; Saiki, Shinji; Soong, Bing-Wen; Swoboda, Kathryn J.; Tucker, Sam; Wood, Nicholas; Hanna, Michael; Bowcock, Anne M.; Szepetowski, Pierre; Fu, Ying-Hui; Ptacek, Louis J. 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Autonomic status epilepticus in Panayiotopoulos syndrome and other childhood and adult epilepsies: A consensus viewPanayiotopoulos综合征和其他儿童和成人癫痫的自主神经癫痫持续状态: 共识Ferrie, Colin D.; Caraballo, Roberto; Covanis, Athanasios; Demirbilek, Veysi; Dervent, Aysin; Fejerman, Natalio; Fusco, Lucia; Grunewald, Richard A.; Kanazawa, Osamu; Koutroumanidis, Michael; Lada, Christina; Livingston, John H.; Nicotra, Alessia; Oguni, Hirokazu; Martinovic, Zarko; Nordli, Douglas R., Jr.; Parisi, Pasquale; Scott, Rod C.; Specchio, Nicola; Verrotti, Alberto; Vigevano, Federico; Walker, Matthew C.; Watanabe, Kazuyoshi; Yoshinaga, Harumi; Panayiotopoulos, Chrysostomos P. 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndromeCaraballo, R; Pavek, S; Lemainque, A; Gastaldi, M; Echenne, B; Motte, J; Genton, P; Cersósimo, R; Humbertclaude, V; Fejerman, N; Monaco, AP; Lathrop, MG; Rochette, J; Szepetowski, P 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 
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