DOI : 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 43 · April 2012 DOI: 10.1055/s-002-23054


Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics
Münster, 19th to 22nd April 2012

Chair: Prof. Dr. med. Gerhard Kurlemann, Münster
Abstracts (HTML) List of Authors
PS19_02
Stülpnagel, C von; Koehler, U; Neuhann, T; Pieper, T; Staudt, M; Kluger, G: Narrowing down the minimal critical region for epilepsy susceptibility in chromosome 5p
PS19_03
Stephani, U; van Baalen, A; Nelle, W: Epileptic seizures with mild gastroenteritis
PS19_04
Linder-Lucht, M; Aznar Lain, G; Vivanco Hidalgo, R; Massot Taurus, A; Herraiz Rocamora, J; Poehler, V; Neubauer, B; Rocamora Zuñiga, R: Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity
PS19_05
Kleiss, R; Muhle, H; Boor, R; Bast, T; Kluger, G; Jacobs, J; Wolff, M; Steiner, G; Reutlinger, C; Spiegler, J; Stephani, U; Helbig, I; Spiczak, S von: Clinical characterization of myoclonic-astatic epilepsy
PS19_06
Häusler, M; Schoberer, M; van Baalen, A; Weis, J; Orlikowsky, T; Schmitt, B; Kluger, G; Opladen, T; Czermin, B; Rudnik-Schöneborn, S; Nolte, K: FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment
PS19_07
Dehn, L; Korn-Merker, E; Pfäfflin, M; Fischbach, H; Frantz, M; Hauser, A; May, T: Burdens of parents with epileptic children – Results of a study using a short-form of the German version of the Impact-on-Family-Scale
PS19_08
Becher, T; Gressnich, M; Barthelmie, A; Weise, S: Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)
PS19_09
Kovacevic-Preradovic, T; Kovanovic, D: Symptomatic epilepsy in patient with Klippel-Trénauney-Weber Syndrome. Case report and review of the literature
PS19_12
Brunner-Krainz, M; Deutschmann, A; Pilhatsch, A; Schalamon, J; Gruber-Sedlmayr, U; Plecko, B: Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report