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Epilepsia|May 14, 2013
Hippocampal hyperexcitability and specific epileptiform activity in a mouse model of Dravet syndromeCamille Liautard, Paolo Scalmani, Giovanni Carriero, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 6, 2006
Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizuresPaolo Scalmani, Raffaella Rusconi, Elena Armatura, et al.
Stem Cells (Dayton, Ohio)|September 25, 2016
Depletion of the Fragile X Mental Retardation Protein in Embryonic Stem Cells Alters the Kinetics of NeurogenesisOlfa Khalfallah, Marielle Jarjat, Laetitia Davidovic, et al.
Human Mutation|April 30, 2009
A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies?Raffaella Rusconi, Romina Combi, Sandrine Cestèle, et al.
Epilepsia|November 1, 2023
Are we there yet? A critical evaluation of sudden and unexpected death in epilepsy modelsJonathon Smith, George Richerson, Hayet Kouchi, et al.
Molecular Autism|January 4, 2022
Rescuing epileptic and behavioral alterations in a Dravet syndrome mouse model by inhibiting eukaryotic elongation factor 2 kinase (eEF2K)Stefania Beretta, Laura Gritti, Luisa Ponzoni, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 1, 2005
Molecular determinants for modulation of persistent sodium current by G-protein betagamma subunitsMassimo Mantegazza, Frank H Yu, Andrew J Powell, et al.
Neurobiology of Disease|February 28, 2025
Neurodevelopmental defects in Dravet syndrome Scn1a+/- mice: Targeting GABA-switch rescues behavioral dysfunctions but not seizures and mortalityLara Pizzamiglio, Fabrizio Capitano, Evgeniia Rusina, et al.
Channels (Austin, Tex.)|June 1, 2012
The 22nd ion channel meeting, september 2011, franceJean-Marc Goaillard, Laurent Groc, Sabine Lévi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2024
Preictal dysfunctions of inhibitory interneurons paradoxically lead to their rebound hyperactivity and to low-voltage-fast onset seizures in Dravet syndromeFabrizio Capitano, Mathieu Kuchenbuch, Jennifer Lavigne, et al.
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