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Husheng Wu

Showing results (11-20 of 22) with videos related to

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Neuroscience Letters|August 15, 2006
New variants in the CACNA1H gene identified in childhood absence epilepsyJianmin Liang, Yuehua Zhang, Juli Wang, 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.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 6, 2002
[Case-control study and transmission/disequilibrium test of childhood absence epilepsy]Jianjun Lu, Yucai Chen, Yuehua Zhang, et al.
Neuroscience Letters|May 29, 2003
The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han populationJianjun Lu, Yucai Chen, Hong Pan, et al.
Neuroscience Letters|October 18, 2002
Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsyJianjun Lu, Yucai Chen, Yuehua Zhang, et al.
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.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 14, 2016
[Diagnosis of mitochondrial disorders in children with next generation sequencing]Zhimei Liu, Fang Fang, Changhong Ding, 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.
Human Genetics|February 28, 2012
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsyYuwu Jiang, Yuehua Zhang, Pingping Zhang, et al.
Clinical Rheumatology|November 28, 2017
Prevalence of psychological disorders, sleep disturbance and stressful life events and their relationships with disease parameters in Chinese patients with ankylosing spondylitisYutong Jiang, Mingcan Yang, Qing Lv, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Neuroscience Letters|August 15, 2006
New variants in the CACNA1H gene identified in childhood absence epilepsyJianmin Liang, Yuehua Zhang, Juli Wang, 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.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 6, 2002
[Case-control study and transmission/disequilibrium test of childhood absence epilepsy]Jianjun Lu, Yucai Chen, Yuehua Zhang, et al.
Neuroscience Letters|May 29, 2003
The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han populationJianjun Lu, Yucai Chen, Hong Pan, et al.
Neuroscience Letters|October 18, 2002
Mutation screen of the GABA(A) receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsyJianjun Lu, Yucai Chen, Yuehua Zhang, et al.
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.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 14, 2016
[Diagnosis of mitochondrial disorders in children with next generation sequencing]Zhimei Liu, Fang Fang, Changhong Ding, 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.
Human Genetics|February 28, 2012
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsyYuwu Jiang, Yuehua Zhang, Pingping Zhang, et al.
Clinical Rheumatology|November 28, 2017
Prevalence of psychological disorders, sleep disturbance and stressful life events and their relationships with disease parameters in Chinese patients with ankylosing spondylitisYutong Jiang, Mingcan Yang, Qing Lv, et al.
Pageof 3