Showing results (41-50 of 114) with videos related to
Sort By:
Pageof 12
Brain & Development|July 19, 2011
Epilepsy in children with methylmalonic acidemia: electroclinical features and prognosisXiuwei Ma, Yuehua Zhang, Yanling Yang, et al.Neuroscience Letters|February 2, 2006
Long-term effect of early discharge on sEPSC and [Ca2+]i in developing neuronsJingmin Wang, Yuwu Jiang, Haiyan Cao, et al.Pediatric Neurology|August 1, 2006
Acute metabolic crisis induced by vaccination in seven Chinese patientsYanling Yang, Sayami Sujan, Fang Sun, et al.Brain & Development|April 10, 2010
Childhood absence epilepsy: Elctroclinical features and diagnostic criteriaXiuwei Ma, Yuehua Zhang, Zhixian Yang, et al.BMC Medical Genetics|September 20, 2017
SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizuresJiaping Wang, Hua Gao, Xinhua Bao, et al.Journal of Human Genetics|July 22, 2016
FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathiesXiaona Fu, Haipo Yang, Cuijie Wei, et al.Journal of Child Neurology|December 13, 2006
Clinical and biochemical studies on Chinese patients with methylmalonic aciduriaYanling Yang, Fang Sun, Jinqing Song, et al.European Journal of Medical Genetics|September 18, 2012
Molecular characteristics of Chinese patients with Rett syndromeXiaoying Zhang, Xinhua Bao, Jingjing Zhang, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 8, 2009
[Mutation analysis of the SCN1A gene in severe myoclonic epilepsy of infancy]Huihui Sun, Yuehua Zhang, Xiaoyan Liu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 3, 2014
[Clinical features and PRRT2 mutations in infantile convulsions with paroxysmal choreoathetosis]Xiaoling Yang, Yuehua Zhang, Xiaojing Xu, et al.Pageof 12