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Neurological Research and Practice|December 16, 2020
Neuro-Sweet syndrome - a rare differential diagnosis in aseptic meningoencephalitisElgin Hoffmann, Christian Boßelmann, Stephan Forchhammer, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|February 26, 2014
Genetic biomarkers in epilepsyYvonne G Weber, Anne T Nies, Matthias Schwab, et al.
Pediatric Neurology|July 9, 2013
Possible effect of corticoids on hemiplegic attacks in severe hemiplegic migraineIciar Sánchez-Albisua, Martin Schöning, Karin Jurkat-Rott, et al.
Stem Cell Research|August 30, 2019
Generation of an induced pluripotent stem cell (iPSC) line (HIHDNEi003-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Thr374Ala) mutationBetül Uysal, Heidi Löffler, Filip Rosa, et al.
Der Nervenarzt|June 28, 2019
[Epileptogenesis and consequences for treatment]Ulrike B S Hedrich, Henner Koch, Albert Becker, et al.
Clinical Pharmacokinetics|April 11, 2015
Impact of Genetic Polymorphisms of ABCB1 (MDR1, P-Glycoprotein) on Drug Disposition and Potential Clinical Implications: Update of the LiteratureStefan Wolking, Elke Schaeffeler, Holger Lerche, et al.
Neuroscience Letters|March 4, 2006
Immunohistochemical analysis of KCNQ3 potassium channels in mouse brainJulia Geiger, Yvonne G Weber, Bernhard Landwehrmeyer, et al.
Plos Computational Biology|March 6, 2023
Predicting functional effects of ion channel variants using new phenotypic machine learning methodsChristian Malte Boßelmann, Ulrike B S Hedrich, Holger Lerche, et al.
Frontiers in Immunology|March 26, 2026
Antineuronal antibody titres in autoimmune encephalitis: clinical implications for diagnosis and long-term immunotherapyHanna Schwab, Josua Kegele, Markus C Kowarik, et al.
Molecular Pharmacology|January 22, 2005
The new anticonvulsant retigabine favors voltage-dependent opening of the Kv7.2 (KCNQ2) channel by binding to its activation gateThomas V Wuttke, Guiscard Seebohm, Sigrid Bail, et al.
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