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Biophysical Journal|March 4, 2006
Modeling of single noninactivating Na+ channels: evidence for two open and several fast inactivated statesYu-Kai The, Jacqueline Fernandes, M Oana Popa, et al.The European Journal of Neuroscience|July 21, 2005
Molecular analysis of the A322D mutation in the GABA receptor alpha-subunit causing juvenile myoclonic epilepsyKlaus Krampfl, Snezana Maljevic, Patrick Cossette, et al.Brain : a Journal of Neurology|March 26, 2002
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type IIAlexey Kuzmenkin, Vanesa Muncan, Karin Jurkat-Rott, et al.Epilepsy Research|January 12, 2007
Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsyAnne Hempelmann, Joana Cobilanschi, Armin Heils, et al.Seizure|November 11, 2017
Periodic EEG patterns in sporadic Creutzfeld-Jakob-Disease can be benzodiazepine-responsive and be difficult to distinguish from non-convulsive status epilepticusJustus Marquetand, Susanne Knake, Adam Strzelczyk, et al.Brain Topography|May 17, 2018
Increased Functional MEG Connectivity as a Hallmark of MRI-Negative Focal and Generalized EpilepsyYiwen Li Hegner, Justus Marquetand, Adham Elshahabi, et al.Stem Cell Research|January 18, 2023
Generation of an induced pluripotent stem cell (iPSC) line from a patient with GEFS+ carrying a STX1B (p.Lys45delinsArgMetCysIleGlu and p.Leu46Met) mutationCarolin Haag, Betül Uysal, Justus Marquetand, et al.Stem Cell Research|May 11, 2019
Establishment of a human induced pluripotent stem cell (iPSC) line (HIHDNEi002-A) from a patient with developmental and epileptic encephalopathy carrying a KCNA2 (p.Arg297Gln) mutationNiklas Schwarz, Betül Uysal, Filip Rosa, et al.Journal of Neurology|July 16, 2014
Focal epilepsy in glucose transporter type 1 (Glut1) defects: case reports and a review of literatureStefan Wolking, Felicitas Becker, Thomas Bast, et al.Stem Cell Research|May 25, 2025
Generation of an induced pluripotent stem cell (iPSC) line carrying a KCNA2 homozygous (p.Arg294His, R294H) mutation related to hereditary spastic paraplegiaHang Lyu, Carolin Haag, Niklas Schwarz, et al.Pageof 28