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European Journal of Medical Genetics|September 13, 2022
A novel homozygous mutation in ERLIN1 gene causing spastic paraplegia 62 and literature reviewZe-Yu Zhu, Zi-Yi Li, Chao Zhang, et al.
Neuroscience Letters|October 17, 2019
Primary familial brain calcification presenting as paroxysmal kinesigenic dyskinesia: Genetic and functional analysesFei-Xia Zhan, Wo-Tu Tian, Chao Zhang, et al.
Clinical Neurology and Neurosurgery|January 15, 2019
Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disordersChao Zhang, Fei-Xia Zhan, Wo-Tu Tian, et al.
Annals of Clinical and Translational Neurology|June 19, 2019
Lysosomal degradation of GMPPB is associated with limb-girdle muscular dystrophy type 2TWo-Tu Tian, Hai-Yan Zhou, Fei-Xia Zhan, et al.
Zoological Research|January 23, 2025
Reciprocal translocation experiments reveal gut microbiome plasticity and host specificity in a Qinghai-Xizang Plateau lizardWei Yu, Jing Yang, Li-Wei Teng, et al.
Annals of Clinical and Translational Neurology|February 6, 2020
New phenotype of DCTN1-related spectrum: early-onset dHMN plus congenital foot deformityWo-Tu Tian, Li-Hua Liu, Hai-Yan Zhou, et al.
Seizure|December 5, 2020
Neurodevelopmental disorder caused by a truncating de novo variant of IRF2BPLXiao-Hang Qian, Xiao-Ying Liu, Ze-Yu Zhu, et al.
Chemical Communications (Cambridge, England)|April 30, 2024
Prussian blue analogue derived from leather waste as a bifunctional catalyst in zinc-air batteriesMeng-Yu Liu, Shi-Yi Shen, Jia-Hua Guo, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 8, 2018
The study of exercise tests in paroxysmal kinesigenic dyskinesiaHai-Yan Zhou, Fei-Xia Zhan, Wo-Tu Tian, et al.
Brain Imaging and Behavior|July 25, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathyFei-Xia Zhan, Ze-Yu Zhu, Qing Liu, et al.
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