Exploring Basic Mechanisms of SUDEP in SCN8A EpilepsyAn SCN8A Unraveled StoryJan 10, 2023Jan 10, 2023
Partnering for Progress in the SCN8A CommunityFamilies are desperate for improved treatments and outcomes for their children with SCN8A epilepsy and related disorders. An exciting new…Nov 5, 2022Nov 5, 2022
SCN8A Genotype-Phenotype Correlations with Katrine Johannesen, MD, PhDAn SCN8A Unraveled StoryJul 6, 2022Jul 6, 2022
Developing an SCN8A ASO with PhD Student, Sophie HillAn SCN8A Unraveled StoryJun 24, 2022Jun 24, 2022
Using Mouse Models to Understand SCN8A Epilepsy with Jennifer Wong, PhDAn SCN8A Unraveled StoryJun 13, 2022Jun 13, 2022
An Update on the International SCN8A Alliance’s Effort to Develop the First Global Consensus on…and Ways to Get Involved!Mar 1, 2022Mar 1, 2022
SCN8A Alliance Loss of Function Family MeetingFinally, a home for the ~10% of families whose children tend to present very differently than those with gain of function mutationsOct 3, 2021Oct 3, 2021
