Hasil Pencarian - Wo-tu TIAN
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1
Clinical phenotype analysis of paroxysmal kinesigenic dyskinesia oleh Wo-tu TIAN, Xiao-jun HUANG, Jun-yi SHEN, Yang-qi XU, Sheng-di CHEN, Li CAO
Diterbitkan 2017-07-01
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2
Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis oleh Yang-Qi Xu, Xiao-Li Liu, Xiao-Jun Huang, Wo-Tu Tian, Hui-Dong Tang, Li Cao
Diterbitkan 2018-01-01
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3
Lysosomal degradation of GMPPB is associated with limb‐girdle muscular dystrophy type 2T oleh Wo‐Tu Tian, Hai‐Yan Zhou, Fei‐Xia Zhan, Ze‐Yu Zhu, Jie Yang, Sheng‐Di Chen, Xing‐Hua Luan, Li Cao
Diterbitkan 2019-06-01
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4
Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18 oleh Wo-Tu Tian, Jun-Yi Shen, Xiao-Li Liu, Tian Wang, Xing-Hua Luan, Hai-Yan Zhou, Sheng-Di Chen, Xiao-Jun Huang, Li Cao
Diterbitkan 2016-01-01
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5
New phenotype of DCTN1‐related spectrum: early‐onset dHMN plus congenital foot deformity oleh Wo‐Tu Tian, Li‐Hua Liu, Hai‐Yan Zhou, Chao Zhang, Fei‐Xia Zhan, Ze‐Yu Zhu, Sheng‐Di Chen, Xing‐Hua Luan, Li Cao
Diterbitkan 2020-02-01
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6
Social and psychological survey on paroxysmal kinesigenic dyskinesia patients in China oleh Wo-tu TIAN, Xiao-jun HUANG, Gui-ling LIANG, Chen-xi ZHU, Ying SHEN, Yu FANG, Mu-han CHEN, Jun-yi SHEN, Sheng-di CHEN, Li CAO
Diterbitkan 2017-08-01
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7
Depression, anxiety, and quality of life in paroxysmal kinesigenic dyskinesia patients oleh Wo-Tu Tian, Xiao-Jun Huang, Xiao-Li Liu, Jun-Yi Shen, Gui-Ling Liang, Chen-Xi Zhu, Wei-Guo Tang, Sheng-Di Chen, Yan-Yan Song, Li Cao
Diterbitkan 2017-01-01
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8
Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy oleh Wo-Tu Tian, Fei-Xia Zhan, Qing Liu, Xing-Hua Luan, Chao Zhang, Liang Shang, Ben-Yan Zhang, Si-Jian Pan, Fei Miao, Jiong Hu, Ping Zhong, Shi-Hua Liu, Ze-Yu Zhu, Hai-Yan Zhou, Suya Sun, Xiao-Li Liu, Xiao-Jun Huang, Jing-Wen Jiang, Jian-Fang Ma, Ying Wang, Shu-Fen Chen, Hui-Dong Tang, Sheng-Di Chen, Li Cao
Diterbitkan 2019-12-01
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