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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 11, 2012
[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome]Xiao-jing Xu, Yue-hua Zhang, Hui-hui Sun, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 10, 2004
[X-linked adrenoleukodystrophy ABCD1 gene mutation analysis in China]Hong Pan, Hui Xiong, Yue-hua Zhang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 21, 2006
[Clinical characteristics and long-term prognosis of Landau-Kleffner syndrome]Shuang Wang, Yue-hua Zhang, Xin-hua Bao, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 18, 2013
[Analysis of HEPACAM mutations in a Chinese family with megalencephalic leukoencephalopathy with subcortical cysts]Mang-mang Guo, Yu-wu Jiang, Han Xie, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|May 18, 2011
[Leucodystrophy induced by late onset 3-hydroxy-3-methylglutaric aciduria]Yan-Yan Ma, Jin-Qing Song, Tong-Fei Wu, et al.
World Journal of Pediatrics : WJP|March 6, 2025
Clinical and genetic characteristics of glucose transporter 1 deficiency syndrome in a large cohort of Chinese patientsMei-Jiao Zhang, Shi-Min Zhang, Qing-Ping Zhang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 18, 2013
[Valproic acid-induced idiosyncratic liver injury in 4 cases]Hui Xiong, Chen-tao Liu, Yue-hua Zhang, et al.
Chinese Medical Journal|March 11, 2016
Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic HybridizationWen-Xu Yang, Hong Pan, Lin Li, et al.
Chinese Medical Journal|June 27, 2015
Different Eukaryotic Initiation Factor 2Bε Mutations Lead to Various Degrees of Intolerance to the Stress of Endoplasmic Reticulum in OligodendrocytesNa Chen, Yu-Wu Jiang, Hong-Jun Hao, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 5, 2024
Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activationXiao Li, Tianshuang Wang, Nana Liu, et al.
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