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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 2, 2024
Domain-specific phenotypes in LINS1-related disorder-A Chinese family with the Q92X variant and literature reviewXu-Ying Li, Zhanjun Wang, Yanping Yang, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|August 25, 2021
A model to assess the risk of peripherally inserted central venous catheter-related thrombosis in patients with breast cancer: a retrospective cohort studySi-Yi Peng, Tao Wei, Xu-Ying Li, et al.
Guang Pu Xue Yu Guang Pu Fen Xi = Guang Pu|March 11, 2015
[Structural, morphological and optical properties of PbI2 thick films]Ding-Yu Yang, Xing-hua Zhu, Hui Sun, et al.
Journal of Pediatric Nursing|April 29, 2026
Exploring the safe dwell time of peripheral venous catheters in pediatric patients: A prospective cohort studyTao Wei, Yan Tan, Mei-Hong Hu, et al.
Neurogenetics|July 15, 2023
Novel mutations and molecular pathways identified in patients with brain iron accumulation disordersLianghao Si, Zhanjun Wang, Xu-Ying Li, et al.
American Journal of Medical Genetics. Part A|July 26, 2024
Clinical, genetic, and neuroimaging profiles of autosomal recessive spinocerebellar ataxia type 4 caused by novel VPS13D variants in ChineseYue Dong, Milan Jia, Shuang Tan, et al.
Zhen Ci Yan Jiu = Acupuncture Research|January 25, 2013
[Involvement of cerebral neuroglobin in electroacupuncture preconditioning-induced protection effect in cerebral ischemia-reperfusion rats]Ya-Ning Xie, Feng Wang, Qiang Wang, et al.
BMC Medical Genomics|September 13, 2021
Sequencing of neurofilament genes identified NEFH Ser787Arg as a novel risk variant of sporadic amyotrophic lateral sclerosis in Chinese subjectsFeng Lin, Wanhui Lin, Chaofeng Zhu, et al.
Chinese Medical Journal|November 15, 2019
Chronic wound biofilms: diagnosis and therapeutic strategiesDi Wei, Xiao-Mei Zhu, Yong-Yi Chen, et al.
Communications Biology|November 25, 2023
ACO2 deficiency increases vulnerability to Parkinson's disease via dysregulating mitochondrial function and histone acetylation-mediated transcription of autophagy genesJunge Zhu, Fanxi Xu, Hong Lai, et al.
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