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Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|February 3, 2004
[Diagnosis and treatment of biotinidase deficiency-clinical study of six patients]Yan-ling Yang, Seiji Yamaguchi, Yasuko Tagami, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 20, 2013
Genetic and biochemical findings in Chinese children with Leigh syndromeYan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, et al.
European Journal of Pediatrics|January 16, 2026
Identification of novel variants in the ARID1B gene causing Coffin-Siris syndromeYan Ge, Xin-Yi Zhang, Xu Han, 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.
Nature Communications|March 23, 2025
Mitochondria transplantation transiently rescues cerebellar neurodegeneration improving mitochondrial function and reducing mitophagy in miceShu-Jiao Li, Qian-Wen Zheng, Jie Zheng, 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.
Redox Biology|December 26, 2021
Targeted up-regulation of Drp1 in dorsal horn attenuates neuropathic pain hypersensitivity by increasing mitochondrial fissionKun-Long Zhang, Shu-Jiao Li, Xue-Yin Pu, et al.
Zhonghua Yi Xue Za Zhi|January 13, 2011
[Analysis of clinical phenotype in 42 nuclear pedigrees carrying mitochondrial DNA A3243G mutation]Yi-nan Ma, Fang Fang, Yan-yan Cao, et al.
The International Journal of Neuropsychopharmacology|March 4, 2020
Upregulation of TRPC6 Mediated by PAX6 Hypomethylation Is Involved in the Mechanical Allodynia Induced by Chemotherapeutics in Dorsal Root GanglionXiang-Zhong Zhang, De-Xing Luo, Xiao-Hui Bai, et al.
Frontiers in Nutrition|May 30, 2023
Case report: An asymptomatic mother with an inborn error of cobalamin metabolism (cblC) detected through high homocysteine levels during prenatal diagnosisYu-Peng Liu, Ru-Xuan He, Zhe-Hui Chen, et al.
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