PUBLIKATIONEN - 2011

Muhle H, Mefford HC, Obermeier T, von Spiczak S, Eichler EE, Stephani U, Sander T, Helbig I. Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome. Epilepsia. 2011 Dec;52(12):e194-8.

von Spiczak S, Finsterwalder K, Muhle H, Franke A, Schilhabel M, Stephani U, Helbig I. Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach. Epilepsia. 2011 Oct;52(10):e143-7.

Ufer M, von Stülpnagel C, Muhle H, Haenisch S, Remmler C, Majed A, Plischke H, Stephani U, Kluger G, Cascorbi I. Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsy. Pharmacogenet Genomics. 2011 Oct;21(10):624-30.

von Spiczak S, Helbig I, Drechsel-Baeuerle U, Muhle H, van Baalen A, van Kempen MJ, Lindhout D, Scheffer IE, Berkovic SF, Stephani U, Keller-Stanislawski B. A Retrospective Population-based Study on Seizures Related to Childhood Vaccination. Epilepsia. 2011 Aug;52(8):1506-12.

von Spiczak, Caliebe A, Muhle H, Helbig I, Stephani U. Genetische Ursachen epileptischer Enzephalopathien. Z Epileptol 2011 24:108–113

Tro-Baumann B*, von Spiczak S*, Lotte J, Bast T, Haberlandt E, Sassen R, Freund A, Leiz S, Stephani U, Boor R, Holthausen H, Helbig I, Kluger G. A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome. Epilepsia. 2011 Jan;52(1):175-8. * These authors contributed equally.