Life-span characterization of epilepsy and comorbidities in Dravet syndrome mice carrying a targeted deletion of exon 1 of the Scn1a gene
Author:
Publisher
Elsevier BV
Subject
Developmental Neuroscience,Neurology
Reference44 articles.
1. Genetic deletion of microRNA-22 blunts the inflammatory transcriptional response to status epilepticus and exacerbates epilepsy in mice;Almeida Silva;Mol. Brain,2020
2. Developmental alterations in firing properties of hippocampal CA1 inhibitory and excitatory neurons in a mouse model of Dravet syndrome;Almog;Neurobiol. Dis.,2021
3. Dravet Syndrome: an overview;Anwar;Cureus,2019
4. Adolescent behavioral abnormalities in a Scn1a(+/−) mouse model of Dravet syndrome;Bahceci;Epilepsy Behav.,2020
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4. EEG band power and phase‐amplitude coupling in patients with Dravet syndrome;Annals of the Child Neurology Society;2024-03-26
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