Neonatal SCN2A encephalopathy: A peculiar recognizable electroclinical sequence
Author:
Publisher
Elsevier BV
Subject
Behavioral Neuroscience,Clinical Neurology,Neurology
Reference17 articles.
1. Phenotypic variability from benign infantile epilepsy to Ohtahara syndrome associated with a novel mutation in SCN2A;Syrbe;Mol Syndromol,2016
2. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders;Wolff;Brain,2017
3. Efficacy of sodium channel blockers in SCN2A early infantile epileptic encephalopathy;Dilena;Brain Dev,2017
4. Lacosamide for SCN2A-related intractable neonatal and infantile seizures;Flor-Hirsch;Epileptic Disord,2018
5. EEG changes and seizure exacerbation in young children treated with carhamazepine;Talwar;Epilepsia,1994
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2. Distinctivein vitrophenotypes in iPSC-derived neurons from patients with gain- and loss-of-functionSCN2Adevelopmental and epileptic encephalopathy;The Journal of Neuroscience;2023-12-26
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