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Epilepsia|August 11, 2021
Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in GermanyAdam Strzelczyk, Milka Pringsheim, Thomas Mayer, et al.Frontiers in Neurology|January 20, 2025
Connectome-based disentangling of epilepsy networks from insular stereoelectroencephalographic leadsKathrin Machetanz, Eliane Weinbrenner, Thomas Volkmar Wuttke, et al.Neurobiology of Disease|September 25, 2025
KV7.2 channel dysfunction delays neuronal maturation and undermines early network development in a hiPSC model of KCNQ2-DEEFilip Rosa, Stephan Theiss, Susanne Krepp, et al.Epilepsia Open|July 17, 2025
Efficacy and tolerability of fenfluramine with concomitant potassium bromide in patients with Dravet syndromeMilka Pringsheim, Gerhard Kluger, Adam Strzelczyk, et al.Journal of Medical Genetics|June 14, 2012
Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy geneMaria Kousi, Verneri Anttila, Angela Schulz, et al.Communications Biology|May 31, 2022
Functional correlates of clinical phenotype and severity in recurrent SCN2A variantsGéza Berecki, Katherine B Howell, Jacqueline Heighway, et al.Neurology. Genetics|June 8, 2017
ARHGEF9 disease: Phenotype clarification and genotype-phenotype correlationMichael Alber, Vera M Kalscheuer, Elysa Marco, et al.Neuropediatrics|October 20, 2015
A Multinational Survey on Actual Diagnostics and Treatment of Subacute Sclerosing PanencephalitisMartin Häusler, Ayse Aksoy, Michael Alber, et al.Neurology|September 2, 2018
The phenotype of SCN8A developmental and epileptic encephalopathyElena Gardella, Carla Marini, Marina Trivisano, et al.Epilepsia|May 23, 2012
Targeted next generation sequencing as a diagnostic tool in epileptic disordersJohannes R Lemke, Erik Riesch, Tim Scheurenbrand, et al.Pageof 3