PCDH19 mutations cause epilepsy and mental retardation limited to females (EFMR) or Dravet-like syndromes. Especially in the first years of life, epilepsy is known to be highly pharmacoresistant. The aim of our study was to evaluate the effectiveness of antiepileptic therapy in patients with PCDH19 mutations.

Effectiveness of antiepileptic therapy in patients with PCDH19 mutations / Lotte, Jan; Bast, Thomas; Borusiak, Peter; Coppola, Antonietta; Cross, J Helen; Dimova, Petia; Fogarasi, Andras; Graneß, Irene; Guerrini, Renzo; Hjalgrim, Helle; Keimer, Reinhard; Korff, Christian M; Kurlemann, Gerhard; Leiz, Steffen; Linder-Lucht, Michaela; Loddenkemper, Tobias; Makowski, Christine; Mühe, Christian; Nicolai, Joost; Nikanorova, Marina; Pellacani, Simona; Philip, Sunny; Ruf, Susanne; Sánchez Fernández, Iván; Schlachter, Kurt; Striano, Pasquale; Sukhudyan, Biayna; Valcheva, Deyana; Vermeulen, R Jeroen; Weisbrod, Tanja; Wilken, Bernd; Wolf, Philipp; Kluger, Gerhard. - In: SEIZURE. - ISSN 1059-1311. - STAMPA. - 35:(2016), pp. 106-110. [10.1016/j.seizure.2016.01.006]

Effectiveness of antiepileptic therapy in patients with PCDH19 mutations

GUERRINI, RENZO;
2016

Abstract

PCDH19 mutations cause epilepsy and mental retardation limited to females (EFMR) or Dravet-like syndromes. Especially in the first years of life, epilepsy is known to be highly pharmacoresistant. The aim of our study was to evaluate the effectiveness of antiepileptic therapy in patients with PCDH19 mutations.
2016
35
106
110
Lotte, Jan; Bast, Thomas; Borusiak, Peter; Coppola, Antonietta; Cross, J Helen; Dimova, Petia; Fogarasi, Andras; Graneß, Irene; Guerrini, Renzo; Hjalg...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1044484
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