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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 17, 2012
[Enzyme analysis of isolated mitochondrial respiratory chain complex III deficiency]Yan-yan Ma, Tong-fei Wu, Yu-peng Liu, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|July 15, 2011
[Leigh syndrome due to mitochondrial respiratory chain complex II deficiency]Yan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|May 17, 2007
[Clinical features and genotype-phenotype studies of 89 Chinese patients with X-linked adrenoleukodystrophy]Li-li Ping, Xin-hua Bao, Ai-hua Wang, et al.
Frontiers in Neurology|October 2, 2025
The relationship between genotype and phenotype in Chinese children with glucose transporter type 1 deficiency syndromeMei-Jiao Zhang, Shi-Min Zhang, Qing-Ping Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 3, 2006
[Analysis of ARSA mutations in a Chinese family with metachromatic leukodystrophy]Jing-min Wang, Yu-wu Jiang, Hui-ping Shi, et al.
CNS Neuroscience & Therapeutics|February 6, 2019
Modeling vanishing white matter disease with patient-derived induced pluripotent stem cells reveals astrocytic dysfunctionLing Zhou, Peng Li, Na Chen, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|March 15, 2008
[Clinical and genetic analysis of a family with Pelizaeus-Merzbacher disease]Hui-fang Wang, Ye Wu, Yu-wu Jiang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 4, 2014
[Episodic central nervous system symptoms with reversible white matter involvement in Chinese patients with X-linked Charcot-Marie-Tooth disease and literatures review]Hai-hua Zhang, Li-guo Gao, Jing-min Wang, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|March 15, 2008
[Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay]Ye Wu, Yu-wu Jiang, Xiao-zhu Wang, et al.
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