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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2021
Advances in hyperekplexia and other startle syndromesFei-Xia Zhan, Shi-Ge Wang, Li CaoNeuroscience 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.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.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.Nature Cell Biology|February 25, 2026
PML targets and resolves structured protein inclusions to mitigate neurodegenerationYang Wang, Jia-Xin Zhu, Fei-Xia Zhan, 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.Translational Neurodegeneration|December 13, 2019
Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathyWo-Tu Tian, Fei-Xia Zhan, Qing Liu, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.Pageof 2