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Movement Disorders : Official Journal of the Movement Disorder Society|January 31, 2023
The Pathogenesis of Paroxysmal Kinesigenic Dyskinesia: Current ConceptsZi-Yi Li, Wo-Tu Tian, Xiao-Jun Huang, et al.Annals of Translational Medicine|February 15, 2020
Complicated paroxysmal kinesigenic dyskinesia associated with SACS mutationsQiang Lu, Liang Shang, Wo Tu Tian, et al.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.Neuromuscular Disorders : NMD|February 10, 2019
Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature reviewWo-Tu Tian, Xing-Hua Luan, Hai-Yan Zhou, 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|April 2, 2018
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature reviewWo-Tu Tian, Xiao-Li Liu, Yang-Qi Xu, et al.Chinese Medical Journal|August 25, 2017
Depression, anxiety, and quality of life in paroxysmal kinesigenic dyskinesia patientsWo-Tu Tian, Xiao-Jun Huang, Xiao-Li Liu, et al.Pageof 2