Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality-Reference-Cited by-同舟云学术

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Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality

Published:2023-04 Issue:4 Volume:45 Page:231-236
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Kawano Osamu,Saito Takashi,Sumitomo Noriko,Takeshita Eri,Shimizu-Motohashi Yuko,Nakagawa Eiji,Mizuma Kanako,Tanifuji Sachiko,Itai Toshiyuki,Miyatake Satoko,Matsumoto Naomichi,Takahashi Yuji,Mizusawa Hidehiro,Sasaki Masayuki

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Unexplained early onset epileptic encephalopathy: exome screening and phenotype expansion;Allen;Epilepsia,2016

2. KCNQ2 encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy;Weckhuysen;Ann Neurol,2012

3. Arthrogryposis multiplex congenita;Gordon;Brain Dev,1998

4. Early-onset scoliosis: current treatment;Cunin;Orthop Traumatol Surg Res,2015

5. Treatment of scoliosis associated with arthrogryposis multiplex congenita;Komolkin;J Pediatr Orthop,2017

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