Epilepsy syndromes during the first year of life and the usefulness of an epilepsy gene panel
Eun Hye Lee (Lee EH)
Clin Exp Pediatr. 2018;61(4):101-107.   Published online 2018 Apr 23     DOI: https://doi.org/10.3345/kjp.2018.61.4.101
Citations to this article as recorded by Crossref logo
Clinical and genetic analysis of benign familial infantile epilepsy caused by PRRT2 gene variant
Yu Gu, Daoqi Mei, Xiaona Wang, Ang Ma, Jinghui Kong, Yaodong Zhang
Frontiers in Neurology.2023;[Epub]     CrossRef
Efficacy and tolerability of oxcarbazepine in the treatment of focal epilepsy in neonates and infants under 3 months of age: A single-center retrospective analysis
Yuping Ma, Jie Deng, Zhengran Fu, Chunhong Chen, Xiaohui Wang, Xu Wang, Jingwen Weng, Yanhua Shen, Xiaoling Wang, Fang Fang
Epilepsy Research.2023; 197: 107240.     CrossRef
Extending the clinical phenotype of SPTAN1: From DEE5 to migraine, epilepsy, and subependymal heterotopias without intellectual disability
Ana Victoria Marco Hernández, Alfonso Caro, Alejandro Montoya Filardi, Miguel Tomás Vila, Sandra Monfort, Beatriz Beseler Soto, Juan José Nieto‐Barceló, Francisco Martínez
American Journal of Medical Genetics Part A.2022; 188(1): 147.     CrossRef
Characteristics of infantile convulsions and choreoathetosis syndrome caused by PRRT2 mutation
Yaxian Deng, Juanyu Xu, Chunmei Yao, Lei Wang, Xiaohuan Dong, Chengsong Zhao
Pediatric Investigation.2022; 6(1): 11.     CrossRef
Sleep architecture in neonatal and infantile onset epilepsies in the first six months of life: A scoping review
Sangeeta Jethwa, Ronit M. Pressler, Didem Kaya, Alexandre N. Datta
European Journal of Paediatric Neurology.2022; 41: 99.     CrossRef
A Rare Case of Lethal Neonatal Rigidity and Multi-Focal Seizure Syndrome
Palanikumar Balasundaram, Melanie Fijas, Suhas Nafday
Cureus.2021;[Epub]     CrossRef
Genomic Investigation of Infantile and Childhood Epileptic Encephalopathies in Kazakhstan: An Urgent Priority
Altynshash Jaxybayeva, Alissa Nauryzbayeva, Assem Khamzina, Meruert Takhanova, Assel Abilhadirova, Anastasia Rybalko, Kymbat Jamanbekova
Frontiers in Neurology.2021;[Epub]     CrossRef
Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy
Allan Bayat, Michael Bayat, Guido Rubboli, Rikke S. Møller
Genes.2021; 12(7): 1051.     CrossRef
The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures
Aalt van Roest, Anouk Van de Vel, Damien Lederer, Berten Ceulemans
European Journal of Paediatric Neurology.2020; 24: 148.     CrossRef
De Novo and Inherited SETD1A Variants in Early-onset Epilepsy
Xiuya Yu, Lin Yang, Jin Li, Wanxing Li, Dongzhi Li, Ran Wang, Kai Wu, Wenhao Chen, Yi Zhang, Zilong Qiu, Wenhao Zhou
Neuroscience Bulletin.2019; 35(6): 1045.     CrossRef
A Child with a c.6923_6928dup (p.Arg2308_Met2309dup) SPTAN1 Mutation Associated with a Severe Early Infantile Epileptic Encephalopathy
Valentina Rapaccini, Susanna Esposito, Francesco Strinati, Mariella Allegretti, Elisabetta Manfroi, Francesco Miconi, Mariabernarda Pitzianti, Paolo Prontera, Nicola Principi, Augusto Pasini
International Journal of Molecular Sciences.2018; 19(7): 1976.     CrossRef