Ketogenic diet as a successful early treatment modality for SCN2A mutation
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference10 articles.
1. SCN2A encephalopathy;Howell;Neurology,2015
2. De novo mutations revealed by whole-exome sequencing are strongly associated with autism;Sanders;Nature,2012
3. Sodium channels, inherited epilepsy, and antiepileptic drugs;Catterall;Annu Rev Pharmacol Toxicol,2014
4. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders;Wolff;Brain,2017
5. The use of ketogenic diet in special situations: expanding use in intractable epilepsy and other neurologic disorders;Lee;Korean J Pediatr,2012
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1. Use of ketogenic dietary therapy for drug‐resistant epilepsy in early infancy;Epilepsia Open;2023-11-20
2. Feasibility of ketogenic diet therapy variants for refractory epilepsy in neonates to infants under 2 years old;Epilepsy & Behavior;2023-09
3. Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first‐line therapies;Epilepsia;2023-05-15
4. Functional analysis of a novel de novo SCN2A variant in a patient with seizures refractory to oxcarbazepine;Frontiers in Molecular Neuroscience;2023-04-20
5. Experience with the ketogenic diet in premature neonates;Epilepsia Open;2022-12
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