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Frontiers in Neurology|June 29, 2019
The Efficacy of Ketogenic Diet in 60 Chinese Patients With Dravet SyndromeXiaojuan Tian, Jiaoyang Chen, Jing Zhang, et al.Developmental Medicine and Child Neurology|November 3, 2019
CHD2-related epilepsy: novel mutations and new phenotypesJiaoyang Chen, Jing Zhang, Aijie Liu, et al.Journal of Human Genetics|December 8, 2017
Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohortQi Zeng, Xiaoling Yang, Jing Zhang, et al.Journal of Human Genetics|December 17, 2010
Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)Jingmin Wang, Jing Shang, Ye Wu, et al.Journal of Human Genetics|June 21, 2008
SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plusHuihui Sun, Yuehua Zhang, Jianmin Liang, et al.Scientific Reports|August 3, 2017
Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencingXiaona Fu, Haipo Yang, Hui Jiao, et al.American Journal of Medical Genetics. Part A|October 21, 2009
Fukutin gene retrotransposal insertion in a non-Japanese Fukuyama congenital muscular dystrophy (FCMD) patientHui Xiong, Shuo Wang, Kazuhiro Kobayashi, et al.Journal of Medical Genetics|October 6, 2018
Mosaicism and incomplete penetrance of PCDH19 mutationsAijie Liu, Xiaoxu Yang, Xiaoling Yang, et al.Epilepsia|March 19, 2015
SCN8A mutations in Chinese children with early onset epilepsy and intellectual disabilityWeijing Kong, Yujia Zhang, Yang Gao, et al.Journal of Child Neurology|July 23, 2013
Disseminated encephalomyelitis-like central nervous system neoplasm in childhoodJianhui Zhao, Xinhua Bao, Na Fu, et al.Pageof 12