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Chinese Medical Journal|October 23, 2004
Case-control study and transmission/disequilibrium tests of the genes encoding GABRA5 and GABRB3 in a Chinese population affected by childhood absence epilepsyJian-jun Lü, Yue-hua Zhang, Hong Pan, et al.
Glia|October 15, 2013
Traumatic scratch injury in astrocytes triggers calcium influx to activate the JNK/c-Jun/AP-1 pathway and switch on GFAP expressionKai Gao, Chen Ran Wang, Feng Jiang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 27, 2007
[Diagnostic value of muscle, sural nerve and skin biopsies in childhood neuromuscular disorders]Xing-zhi Chang, Jia-yun Zhou, Yun Yuan, et al.
Zhonghua Yi Xue Za Zhi|August 19, 2003
[Association of child absence epilepsy with T-STAR gene]Yu-cai Chen, Yue-hua Zhang, Jian-jun Lü, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|December 21, 2010
[Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy]Yan-zhi Zhang, Hui Xiong, Xiao-zhu Wang, et al.
Plos One|April 18, 2012
High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disabilityXiaohong Gong, Yu-Wu Jiang, Xin Zhang, et al.
World Journal of Pediatrics : WJP|August 3, 2019
Identification in Chinese patients with GLIALCAM mutations of megalencephalic leukoencephalopathy with subcortical cysts and brain pathological study on Glialcam knock-in mouse modelsZhen Shi, Hui-Fang Yan, Bin-Bin Cao, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|October 15, 2013
[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome]Yan-yan Liu, Xin-hua Bao, Shuang Wang, et al.
CNS Neuroscience & Therapeutics|August 2, 2019
Clinical features and surgical outcomes in young children with focal cortical dysplasia type IITian-Shuang Wang, Qing-Zhu Liu, Ming Liu, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|February 19, 2014
[Value of muscle enzyme analysis in differential diagnosis of childhood myopathic hyper-creatine kinase-emia]Bing Mao, Hui Xiong, Hui Jiao, et al.
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