Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern-Reference-Cited by-同舟云学术

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Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern

Published:2020-07 Issue: Volume:163 Page:106323
ISSN:0920-1211
Container-title:Epilepsy Research
language:en
Short-container-title:Epilepsy Research

Author:

Lee Sangbo,Kim Se Hee,Kim Borahm,Lee Seung-Tae,Choi Jong Rak,Kim Heung Dong,Lee Joon Soo,Kang Hoon-Chul

Funder

faculty research grant of Yonsei University College of Medicine

Korea Health Technology R&D Project through the Korea Health Industry Development Institute

Ministry of Health & Welfare, Republic of Korea

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference54 articles.

1. Biallelic SCN2A gene mutation causing early infantile epileptic encephalopathy: case report and review;AlSaif;J. Cent. Nerv. Syst. Dis.,2019

2. What does burst suppression really mean?;Amzica;Epilepsy Behav.,2015

3. Neonatal epilepsy genetics;Axeen;Semin. Fetal Neonatal Med.,2018

4. Novel DOCK7 mutations in a Chinese patient with early infantile epileptic encephalopathy 23;Bai;Chin. Med. J.,2019

5. Early-onset epileptic encephalopathies: ohtahara syndrome and early myoclonic encephalopathy;Beal;Pediatr. Neurol.,2012

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