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Neuroscience Letters|April 5, 2003
T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han populationYucai Chen, Jianjun Lu, Yuehua Zhang, et al.Advances in Neurobiology|October 19, 2018
Large De Novo Microdeletion in Epilepsy with Intellectual and Developmental Disabilities, with a Systems Biology AnalysisKai Gao, Yujia Zhang, Ling Zhang, et al.Brain & Development|October 10, 2007
Alpers syndrome with prominent white matter changesXinhua Bao, Ye Wu, Lee-Jun C Wong, et al.Human Genome Variation|April 16, 2016
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathyTetsuya Oda, Hui Xiong, Kazuhiro Kobayashi, et al.Clinical Genetics|March 21, 2019
ATP1A3 mosaicism in families with alternating hemiplegia of childhoodXiaoling Yang, Xiaoxu Yang, Jiaoyang Chen, et al.Pediatric Neurology|June 19, 2012
Allelic variations of glut-1 deficiency syndrome: the chinese experienceYanyan Liu, Xinhua Bao, Dong Wang, et al.Biochemical Genetics|July 25, 2020
Nuclear Factor-κB Pathway Mediates the Molecular Pathogenesis of LMNA-Related Muscular DystrophiesYanbin Fan, Dandan Tan, Xu Zhang, et al.Human Mutation|June 23, 2015
Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet SyndromeXiaojing Xu, Xiaoxu Yang, Qixi Wu, et al.Annals of Neurology|August 2, 2003
Association between genetic variation of CACNA1H and childhood absence epilepsyYucai Chen, Jianjun Lu, Hong Pan, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 3, 2004
[Diagnosis and treatment of biotinidase deficiency-clinical study of six patients]Yan-ling Yang, Seiji Yamaguchi, Yasuko Tagami, et al.Pageof 12