Complicated paroxysmal kinesigenic dyskinesia associated with SACS mutations

af Lu, Qiang, Shang, Liang, Tian, Wo Tu, Cao, Li, Zhang, Xue, Liu, Qing
Udgivet i Ann Transl Med (2020)

Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis

af Xu, Yang-Qi, Liu, Xiao-Li, Huang, Xiao-Jun, Tian, Wo-Tu, Tang, Hui-Dong, Cao, Li
Udgivet i Chin Med J (Engl) (2018)

Lysosomal degradation of GMPPB is associated with limb‐girdle muscular dystrophy type 2T

af Tian, Wo‐Tu, Zhou, Hai‐Yan, Zhan, Fei‐Xia, Zhu, Ze‐Yu, Yang, Jie, Chen, Sheng‐Di, Luan, Xing‐Hua, Cao, Li
Udgivet i Ann Clin Transl Neurol (2019)

Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18

af Tian, Wo-Tu, Shen, Jun-Yi, Liu, Xiao-Li, Wang, Tian, Luan, Xing-Hua, Zhou, Hai-Yan, Chen, Sheng-Di, Huang, Xiao-Jun, Cao, Li
Udgivet i Chin Med J (Engl) (2016)

New phenotype of DCTN1‐related spectrum: early‐onset dHMN plus congenital foot deformity

af Tian, Wo‐Tu, Liu, Li‐Hua, Zhou, Hai‐Yan, Zhang, Chao, Zhan, Fei‐Xia, Zhu, Ze‐Yu, Chen, Sheng‐Di, Luan, Xing‐Hua, Cao, Li
Udgivet i Ann Clin Transl Neurol (2020)

Depression, Anxiety, and Quality of Life in Paroxysmal Kinesigenic Dyskinesia Patients

af Tian, Wo-Tu, Huang, Xiao-Jun, Liu, Xiao-Li, Shen, Jun-Yi, Liang, Gui-Ling, Zhu, Chen-Xi, Tang, Wei-Guo, Chen, Sheng-Di, Song, Yan-Yan, Cao, Li
Udgivet i Chin Med J (Engl) (2017)

Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy

af Tian, Wo-Tu, Zhan, Fei-Xia, Liu, Qing, Luan, Xing-Hua, Zhang, Chao, Shang, Liang, Zhang, Ben-Yan, Pan, Si-Jian, Miao, Fei, Hu, Jiong, Zhong, Ping, Liu, Shi-Hua, Zhu, Ze-Yu, Zhou, Hai-Yan, Sun, Suya, Liu, Xiao-Li, Huang, Xiao-Jun, Jiang, Jing-Wen, Ma, Jian-Fang, Wang, Ying, Chen, Shu-Fen, Tang, Hui-Dong, Chen, Sheng-Di, Cao, Li
Udgivet i Transl Neurodegener (2019)