DOI : 10.1055/s-00000041

Neuropediatrics

Issue 01 · Volume 35 · February 2004 DOI: 10.1055/s-002-3101


Abstracts for the 30th Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)
Bern, Switzerland, March 25–28, 2004

M. Steinlin

P2
Wohlrab, G.; Uyanik, G.; Gross, C.; Hehr, U.; Schmitt, B.; Boltshauser, E.: Familial West syndrome and dystonia caused by ARX gene mutation
P3
Roschitz, B.; Gruber-Sedlmayr, U.; Claes, L.; De Jonghe, P.; Plecko, B.: SCN1A gene mutations in two patients with severe infantile epileptic encephalopathy
P5
Sälke-Kellermann, R.; Weissert, M.; Dorn, T.: Epilepsy in children with inv dup(15)
P8
Völkl-Kernstock, S.; Willinger, U.; Feucht, M.: Cognitive disabilities of children with a benign partial epilepsy
P9
Baumeister, F. A. M.; Liebhaber, G.; Oberhoffer, R.; Gempel, K.; Freisinger, P.; Holthausen, H.: Fatal propofol infusion syndrome in association with ketogenic diet in a child with catastrophic epilepsy
P10
Jourdan Moser, S.; Lütschg, J.: EEG characteristics in Rett syndrome
P13
Bruhn, K.; Rinnert, S.; Stephani, U.: Paroxysmal dystonic choreoathetosis
P18
Berg, J.; Kluger, G.; Redbrake, A.; Holthausen, H.: Ethosuximide is the drug of choice against epileptic negative myoclonus (ENM)
P19
Gerstner, T.; Demirakca, T.; Göppel, C.; Sungurtekin, I.; Brauss, D. F.; König, S. A.: Functional-MRI for school-aged children with neonatal phenobarbitone medication