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Journal of Computational Neuroscience|October 18, 2019
Modeling cortical spreading depression induced by the hyperactivity of interneuronsMathieu Desroches, Olivier Faugeras, Martin Krupa, et al.
Genes, Brain, and Behavior|September 1, 2025
Sex-Specific Behavioral Features of Juvenile and Adult Haploinsufficient Scn2a+/- Female Mice, Model of Autism Spectrum DisorderWendy Marcantonio, Martina Simonti, Isabelle Léna, et al.
Journal of Mathematical Biology|May 12, 2023
Idealized multiple-timescale model of cortical spreading depolarization initiation and pre-epileptic hyperexcitability caused by NaV1.1/SCN1A mutationsLouisiane Lemaire, Mathieu Desroches, Martin Krupa, et al.
Epilepsy Research|September 11, 2010
Epileptogenic ion channel mutations: from bedside to bench and, hopefully, back againMassimo Mantegazza, Raffaella Rusconi, Paolo Scalmani, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 9, 2013
Nonfunctional NaV1.1 familial hemiplegic migraine mutant transformed into gain of function by partial rescue of folding defectsSandrine Cestèle, Emanuele Schiavon, Raffaella Rusconi, et al.
Genes, Brain, and Behavior|January 18, 2019
Hyperactive and anxiolytic-like behaviors result from loss of COUP-TFI/Nr2f1 in the mouse cortexThomas Contesse, Marion Ayrault, Massimo Mantegazza, et al.
Neuropharmacology|June 3, 2017
Post-translational dysfunctions in channelopathies of the nervous systemBenedetta Terragni, Paolo Scalmani, Silvana Franceschetti, et al.
Journal of Neurochemistry|September 1, 2023
Voltage-gated sodium channels in genetic epilepsy: up and down of excitabilityEvgeniia Rusina, Martina Simonti, Fabrice Duprat, et al.
The Lancet. Neurology|March 20, 2010
Voltage-gated sodium channels as therapeutic targets in epilepsy and other neurological disordersMassimo Mantegazza, Giulia Curia, Giuseppe Biagini, et al.
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