SCN2Aencephalopathy-Reference-Cited by-同舟云学术

SCN2Aencephalopathy

Published:2015-08-19 Issue:11 Volume:85 Page:958-966
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Howell Katherine B.,McMahon Jacinta M.,Carvill Gemma L.,Tambunan Dimira,Mackay Mark T.,Rodriguez-Casero Victoria,Webster Richard,Clark Damian,Freeman Jeremy L.,Calvert Sophie,Olson Heather E.,Mandelstam Simone,Poduri Annapurna,Mefford Heather C.,Harvey A. Simon,Scheffer Ingrid E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference39 articles.

1. Sodium channels and the neurobiology of epilepsy

2. Sodium-channel defects in benign familial neonatal-infantile seizures

3. Benign familial neonatal-infantile seizures: Characterization of a new sodium channelopathy

4. A Nonsense Mutation of the Sodium Channel Gene SCN2A in a Patient with Intractable Epilepsy and Mental Decline

5. Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome

Cited by 206 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Categorizing Monogenic Epilepsies by Genetic Mechanisms May Predict Efficacy of the Ketogenic Diet;Pediatric Neurology;2024-11

2. A Neonate with Epileptic Encephalopathy;NeoReviews;2024-08-01

3. The contribution of Na_V1.6 to the efficacy of voltage‐gated sodium channel inhibitors in wild type and Na_V1.6 gain‐of‐function (GOF) mouse seizure control;British Journal of Pharmacology;2024-06-24

4. Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders;Brain;2024-04-23

5. An iPSC line (FINi003-A) from a male with late-onset developmental and epileptic encephalopathy caused by a heterozygous p.E1211K variant in the SCN2A gene encoding the voltage-gated sodium channel Nav1.2;Stem Cell Research;2024-04