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Journal of Human Genetics|May 1, 2010
Analysis of SCN1A mutation and parental origin in patients with Dravet syndromeHuihui Sun, Yuehua Zhang, Xiaoyan Liu, et al.
Annals of the Academy of Medicine, Singapore|November 12, 2009
Outcome of organic acidurias in ChinaYanling Yang, Zhang Yao, Jinqing Song, et al.
Zhonghua Yi Xue Za Zhi|August 27, 2002
[Association analysis of childhood absence epilepsy by microsatellite DNA]Jianjun Lu, Yucai Chen, Hong Pan, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 14, 2015
[Phenotypes and PRRT2 mutation analysis in families with benign familial infantile epilepsy]Xiaoling Yang, Yuehua Zhang, Xiaojing Xu, et al.
Developmental Medicine and Child Neurology|March 25, 2018
The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndromeXiaojuan Tian, Jintang Ye, Qi Zeng, et al.
Pediatric Neurology|August 31, 2006
CACNA1I is not associated with childhood absence epilepsy in the Chinese Han populationJuli Wang, Yuehua Zhang, Jianmin Liang, et al.
Seizure|May 22, 2019
Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutationsJing Zhang, Jiaoyang Chen, Qi Zeng, et al.
Epilepsy Research|May 5, 2019
De novo SCN1A, SCN8A, and CLCN2 mutations in childhood absence epilepsyHan Xie, Wenting Su, Jinrui Pei, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2017
[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome]Qi Zeng, Yuehua Zhang, Xiaoling Yang, et al.
Neuroscience Letters|August 15, 2006
New variants in the CACNA1H gene identified in childhood absence epilepsyJianmin Liang, Yuehua Zhang, Juli Wang, et al.
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