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Stem Cell Research|October 8, 2018
Generation of an induced pluripotent stem cell (iPSC) line from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Leu328Val) mutationNiklas Schwarz, Betül Uysal, Filip Rosa, et al.
Epilepsia Open|December 18, 2022
Safety and tolerability of short-term infusions of intravenous lacosamide in pediatric patients with epilepsy: An open-label, phase 2/3 trialMark Kristof Farkas, Cynthia Beller, Ali Bozorg, et al.
BMC Neurology|November 27, 2013
Encephalopathic Susac's Syndrome associated with livedo racemosa in a young woman before the completion of family planningMaik Engeholm, Beate Leo-Kottler, Hansjörg Rempp, et al.
Neuroimage|March 24, 2015
Multimodal effective connectivity analysis reveals seizure focus and propagation in musicogenic epilepsySilke Klamer, Sabine Rona, Adham Elshahabi, et al.
The Journal of Physiology|November 17, 2007
Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsyThomas V Wuttke, Johann Penzien, Michael Fauler, et al.
Current Opinion in Neurology|January 22, 2019
Spectrum of GABAA receptor variants in epilepsySnezana Maljevic, Rikke S Møller, Christopher A Reid, et al.
Human Mutation|September 14, 2011
Temperature and pharmacological rescue of a folding-defective, dominant-negative KV 7.2 mutation associated with neonatal seizuresSnezana Maljevic, Georgios Naros, Özlem Yalçin, et al.
Seizure|April 23, 2013
Mutation in the mitochondrial tRNA(Ile) gene causes progressive myoclonus epilepsyGábor Zsurka, Felicitas Becker, Markus Heinen, et al.
Epilepsia|June 27, 2025
Recurrent c.-11C>T change located upstream of the normal ATG initiation codon of ANKH causes self-limited familial infantile epilepsyJosua Kegele, Hendrik Juenger, Harald Frantzmann, et al.
Brain Communications|February 23, 2026
Comprehensive evaluation of EEG spatial sampling, head modelling and parcellation effects on network alterations in idiopathic generalized epilepsyChristina Stier, Markus Loose, Carmen Loew, et al.
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