Showing results (21-30 of 102) with videos related to

Sort By:
Pageof 11
Neuroscience Letters|March 7, 2006
Association of BRD2 polymorphisms with photoparoxysmal responseSusanne Lorenz, Kirsten P Taylor, Anne Gehrmann, et al.
Neuroimage|December 18, 2007
Changes in activity of striato-thalamo-cortical network precede generalized spike wave dischargesFriederike Moeller, Hartwig R Siebner, Stephan Wolff, et al.
Neuropediatrics|May 12, 2020
Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification of KCNC2 as a Novel Candidate Gene for EpilepsyAnnika Rademacher, Niklas Schwarz, Simone Seiffert, et al.
Epilepsia|November 5, 2011
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndromeHiltrud Muhle, Heather C Mefford, Tanja Obermeier, et al.
Epilepsy Research|March 22, 2017
Gene expression analysis in untreated absence epilepsy demonstrates an inconsistent patternMarkus von Deimling, Robert Häsler, Verena Steinbach, et al.
Epilepsy Research|November 20, 2013
Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsiesJohanna A Jähn, Sarah von Spiczak, Hiltrud Muhle, et al.
Neuroscience Letters|January 13, 2006
Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivitySusanne Lorenz, Armin Heils, Kirsten P Taylor, et al.
Pharmacogenetics and Genomics|July 30, 2011
Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsyMike Ufer, Celina von Stülpnagel, Hiltrud Muhle, et al.
Epilepsia|February 13, 2013
Variability of EEG-fMRI findings in patients with SCN1A-positive Dravet syndromeJan Moehring, Sarah von Spiczak, Friederike Moeller, et al.
Epilepsia|July 25, 2007
Hemodynamic responses to interictal epileptiform discharges in children with symptomatic epilepsyJulia Jacobs, Eliane Kobayashi, Rainer Boor, et al.
Pageof 11