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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.Journal of Neurology|June 17, 2017
The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizuresKarl Martin Klein, Manuela Pendziwiat, Anda Eilam, et al.Ebiomedicine|June 27, 2022
Predicting the functional effects of voltage-gated potassium channel missense variants with multi-task learningChristian Malte Boßelmann, Ulrike B S Hedrich, Peter Müller, et al.Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.Epilepsy Research|April 21, 2018
Early mortality in SCN8A-related epilepsiesKatrine M Johannesen, Elena Gardella, Ingrid Scheffer, et al.Developmental Medicine and Child Neurology|October 17, 2012
Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variationsSilke Appenzeller, Ingo Helbig, Ulrich Stephani, et al.Seminars in Pediatric Neurology|March 3, 2015
Status epilepticus and refractory status epilepticus managementNicholas S Abend, David Bearden, Ingo Helbig, 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.Basic Research in Cardiology|November 3, 2022
Desmin intermediate filaments and tubulin detyrosination stabilize growing microtubules in the cardiomyocyteAlexander K Salomon, Sai Aung Phyo, Naima Okami, et al.Pageof 33