Last Updated: 09/26/2026
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Found 91 publications
In vivo adenine base editing ameliorates Dravet syndrome phenotypes in a mouse model.
Journal: Science translational medicine
Published: May 13, 2026
Characterizing SCN1A-Related Disorders Using Real-World Data Across 681 Patient-Years.
Journal: medRxiv : the preprint server for health sciences
Published: March 23, 2026
Developmental dysregulation of chandelier cell excitability in a mouse model of Dravet Syndrome.
Journal: bioRxiv : the preprint server for biology
Published: February 12, 2026
Use-dependent regulation of the axonal action potential in parvalbumin-expressing interneurons.
Journal: bioRxiv : the preprint server for biology
Published: February 12, 2026
A hit for base editing: treatment of developmental epilepsy in a mouse model.
Journal: The Journal of clinical investigation
Published: February 02, 2026
An epilepsy-associated KV3.1 potassium channel variant acts via dominant-positive effect.
Journal: The Journal of general physiology
Published: December 29, 2025
Genetic testing for familial epilepsies: Diagnostic yield and genetic findings.
Journal: Epilepsia
Published: December 02, 2025
Flip of the Switch: Targeting GABA Dysregulation to Treat Nonseizure Comorbidities in Dravet Syndrome.
Journal: Epilepsy currents
Published: November 17, 2025
Novel mouse model reveals neurodevelopmental origin of PMM2-CDG brain pathology.
Journal: bioRxiv : the preprint server for biology
Published: June 12, 2025
Interneurons exhibit attenuated ectopic action potential firing in a severe neurodevelopmental disorder.
Journal: Journal of neurophysiology
Published: May 07, 2025
Last Updated: 09/26/2026