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searching for SCN8A 6 found (17 total)

alternate case: sCN8A

Epilepsy-intellectual disability in females (4,237 words) [view diff] exact match in snippet view article find links to article

2016-08-22. "PCDH19 and SCN8A Research Funded By The Cute Syndrome". The Cute Syndrome Foundation: Funding PCDH19 Epilepsy & SCN8A Epilepsy Research. Retrieved

Sudden unexpected death in epilepsy (2,710 words) [view diff] exact match in snippet view article find links to article

identified with LQT8. The sodium ion channel genes SCN1A, SCN1B, SCN2A, and SCN8A and the potassium channel KCNA1 have been implicated in both epilepsy and

Dravet syndrome (4,117 words) [view diff] exact match in snippet view article find links to article

unlike SCN1A mutations, patients often respond to sodium channel blockers. - SCN8A: This gene encodes the alpha-8 subunit (Nav1.6) and is primarily expressed

Amitriptyline (8,668 words) [view diff] exact match in snippet view article find links to article

2018). "A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsy". Epilepsia. 59 (4): 802–813. doi:10.1111/epi.14037. PMID 29574705

Epilepsy syndromes (5,228 words) [view diff] exact match in snippet view article find links to article

KCNQ3 in self-limited neonatal epilepsy, PRRT2 or less commonly SCN2A or SCN8A in self-limited infantile epilepsy and SCN2A or KCNQ2 in self-limited neonatal-infantile

Stephen Waxman (4,692 words) [view diff] exact match in snippet view article find links to article

Restifo, L.L., Erickson, R.P., Hammer, M.F. De novo pathogenic mutation of SCN8A identified by whole genome sequencing of a family quartet with infantile