Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 6 publications
SCN8A Epilepsy, Developmental Encephalopathy, and Related Disorders.
Journal: Pediatric neurology
Published: April 04, 2021
Fenfluramine HCl (Fintepla® ) provides long-term clinically meaningful reduction in seizure frequency: Analysis of an ongoing open-label extension study.
Journal: Epilepsia
Published: May 15, 2020
Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial.
Journal: Lancet (London, England)
Published: November 21, 2018
Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
Journal: Epilepsia
Published: March 19, 2013
De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Journal: American journal of human genetics
Published: November 28, 2011
Showing 1-6 of 6
Last Updated: 09/26/2026