Zhaoxia Wang (Li Cao)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 47

Top Venues

Movement disorders : official journal of the Movement Disorder Society

Annals of clinical and translational neurology

Translational neurodegeneration

Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Shanghai Jiao Tong University Medical School Affiliated Ruijin Hospital

Central South University Xiangya School of Medicine (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Shanghai Jiao Tong University Medical School Affiliated Ruijin Hospital Jul 24 2006 - Aug 31 2020

China

Dr. :: neurology

Education History

Central South University Xiangya School of Medicine

China

PHD :: neurology

Publications

Jingying Wu, Xin Cheng, Duxin Ji, Huiwen Niu, Songquan Yao, Xukun Lv, Jianqiang Wang, Ziyi Li, Haoran Zheng, Yuwen Cao, Feixia Zhan, Mengyuan Zhang, Wotu Tian, Xiaojun Huang, Xinghua Luan, Zhaoxia Wang
The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China. Movement disorders : official journal of the Movement Disorder Society 39 (5) (2024)
Yuwen Cao, Haoran Zheng, Zeyu Zhu, Li Yao, Wotu Tian, Zhaoxia Wang
Clinical and Genetic Spectrum in a Large Cohort of Hereditary Spastic Paraplegia. Movement disorders : official journal of the Movement Disorder Society 39 (4) (2024)
Li Yao, Yuwen Cao, Chao Zhang, Xiaojun Huang, Wotu Tian, Zhaoxia Wang
Clinical and genetic characteristics in a Chinese cohort of complex spastic paraplegia type 4. Clinical genetics (2024)
Li Yao, Yuwen Cao, Chao Zhang, Xiaojun Huang, Wotu Tian, Zhaoxia Wang
Clinical and genetic characteristics in a Chinese cohort of complex spastic paraplegia type 4. Clinical genetics 106 (1) (2024)
Huichun Luo, Xiaojun Huang, Ziyi Li, Wotu Tian, Kan Fang, Taotao Liu, Shige Wang, Beisha Tang, Ji Hu, Ti-Fei Yuan, Zhaoxia Wang
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11 (12) (2024)
Li Yao, Yuwen Cao, Chao Zhang, Xiaojun Huang, Wotu Tian, Zhaoxia Wang
Clinical and genetic characteristics in a Chinese cohort of complex spastic paraplegia type 4. Clinical genetics 106 (1) (2024)
Jingying Wu, Xin Cheng, Duxin Ji, Huiwen Niu, Songquan Yao, Xukun Lv, Jianqiang Wang, Ziyi Li, Haoran Zheng, Yuwen Cao, Feixia Zhan, Mengyuan Zhang, Wotu Tian, Xiaojun Huang, Xinghua Luan, Zhaoxia Wang
The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China. Movement disorders : official journal of the Movement Disorder Society 39 (5) (2024)
Yuwen Cao, Haoran Zheng, Zeyu Zhu, Li Yao, Wotu Tian, Zhaoxia Wang
Clinical and Genetic Spectrum in a Large Cohort of Hereditary Spastic Paraplegia. Movement disorders : official journal of the Movement Disorder Society (2024)
Huichun Luo, Xiaojun Huang, Ziyi Li, Wotu Tian, Kan Fang, Taotao Liu, Shige Wang, Beisha Tang, Ji Hu, Ti-Fei Yuan, Zhaoxia Wang
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11 (12) (2024)
Huichun Luo, Xiaojun Huang, Ziyi Li, Wotu Tian, Kan Fang, Taotao Liu, Shige Wang, Beisha Tang, Ji Hu, Ti-Fei Yuan, Zhaoxia Wang
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia. Advanced science (Weinheim, Baden-Wurttemberg, Germany) 11 (12) (2024)
Huichun Luo, Xiaojun Huang, Ziyi Li, Wotu Tian, Kan Fang, Taotao Liu, Shige Wang, Beisha Tang, Ji Hu, Ti-Fei Yuan, Zhaoxia Wang
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia. Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Huichun Luo, Xiaojun Huang, Ziyi Li, Wotu Tian, Kan Fang, Taotao Liu, Shige Wang, Beisha Tang, Ji Hu, Ti-Fei Yuan, Zhaoxia Wang
An Electroencephalography Profile of Paroxysmal Kinesigenic Dyskinesia. Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2024)
Jingying Wu, Zhaoxia Wang
Reply to: Heterogeneity of CSF1R-RD: Genes, Environment, or Both? Movement disorders : official journal of the Movement Disorder Society 39 (7) (2024)
Jingying Wu, Zhaoxia Wang
Reply to: Heterogeneity of CSF1R-RD: Genes, Environment, or Both? Movement disorders : official journal of the Movement Disorder Society 39 (7) (2024)
Jingying Wu, Xin Cheng, Duxin Ji, Huiwen Niu, Songquan Yao, Xukun Lv, Jianqiang Wang, Ziyi Li, Haoran Zheng, Yuwen Cao, Feixia Zhan, Mengyuan Zhang, Wotu Tian, Xiaojun Huang, Xinghua Luan, Zhaoxia Wang
The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China. Movement disorders : official journal of the Movement Disorder Society (2024)
Zi-Yi Li, Wo-Tu Tian, Xiao-Jun Huang, Zhaoxia Wang
The Pathogenesis of Paroxysmal Kinesigenic Dyskinesia: Current Concepts. Movement disorders : official journal of the Movement Disorder Society (2023)
Jingying Wu, Taotao Liu, Benyan Zhang, Chang Liu, Xinghua Luan, Zhaoxia Wang
An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia. Translational neurodegeneration 12 (1) (2023)
Wotu Tian, Li Yao, Guochao Shi, Ranran Dai, Zhaoxia Wang
A novel DCTN1 mutation causing perry syndrome leads to abnormal splicing of mRNA: genetic and functional analyses. Acta neurologica Belgica (2023)
Zeyu Zhu, Wenzhe Hou, Yuwen Cao, Haoran Zheng, Wotu Tian, Zhaoxia Wang
Spastic paraplegia type 76 due to novel CAPN1 mutations: three case reports with literature review. Neurogenetics (2023)
Li Yao, Zeyu Zhu, Chao Zhang, Wotu Tian, Zhaoxia Wang
PLP1 gene mutations cause spastic paraplegia type 2 in three families. Annals of clinical and translational neurology 10 (3) (2023)
Jingying Wu, Taotao Liu, Benyan Zhang, Chang Liu, Xinghua Luan, Zhaoxia Wang
An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia. Translational neurodegeneration 12 (1) (2023)
Li Yao, Zeyu Zhu, Chao Zhang, Wotu Tian, Zhaoxia Wang
PLP1 gene mutations cause spastic paraplegia type 2 in three families. Annals of clinical and translational neurology 10 (3) (2023)
Jingying Wu, Taotao Liu, Benyan Zhang, Chang Liu, Xinghua Luan, Zhaoxia Wang
An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia. Translational neurodegeneration 12 (1) (2023)
Li Yao, Zeyu Zhu, Chao Zhang, Wotu Tian, Zhaoxia Wang
PLP1 gene mutations cause spastic paraplegia type 2 in three families. Annals of clinical and translational neurology (2023)
Jingying Wu, Taotao Liu, Benyan Zhang, Chang Liu, Xinghua Luan, Zhaoxia Wang
An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia. Translational neurodegeneration 12 (1) (2023)
Jingying Wu, Taotao Liu, Benyan Zhang, Chang Liu, Xinghua Luan, Zhaoxia Wang
An AARS1 variant identified to cause adult-onset leukoencephalopathy with neuroaxonal spheroids and pigmented glia. Translational neurodegeneration 12 (1) (2023)
Xiaoli Liu, Huiyi Ke, Xiaohang Qian, Shige Wang, Feixia Zhan, Ziyi Li, Wotu Tian, Xiaojun Huang, Bin Zhang, Zhaoxia Wang
Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia. Journal of neurology 269 (9) (2022)
Zhouwei Xu, Jingyan Xiang, Xinghua Luan, Zhi Geng, Zhaoxia Wang
Novel compound heterozygous mutations in a GNE myopathy with congenital thrombocytopenia: A case report and literature review. Clinical case reports 10 (4) (2022)
Wotu Tian, Haoran Zheng, Zeyu Zhu, Chao Zhang, Xinghua Luan, Zhaoxia Wang
New phenotype of RTN2-related spectrum: Complicated form of spastic paraplegia-12. Annals of clinical and translational neurology 9 (8) (2022)
Rui Ban, Robert Kopajtich, Junlan Lv, Sarah L Stenton, Masaru Shimura, Zhaoxia Wang, Yun Yuan, Junling Wang, Xiaodi Han, Zhimei Liu, Qiang Shi, Chuanqiang Pu, Holger Prokisch, Fang Fang, Matthias Elstner
The phenotypic spectrum of COX20-associated mitochondrial disorder. Brain : a journal of neurology (2022)
Jingying Wu, Yikang Cao, Mengting Li, Binyin Li, Xize Jia, Zhaoxia Wang
Altered intrinsic brain activity in patients with CSF1R-related leukoencephalopathy. Brain imaging and behavior 16 (4) (2022)
Yuwen Cao, Wotu Tian, Jingying Wu, Xingwang Song, Zhaoxia Wang, Xinghua Luan
DNA hypermethylation of NOTCH2NLC in neuronal intranuclear inclusion disease: a case-control study. Journal of neurology 269 (11) (2022)
Haoran Zheng, Xiaohang Qian, Wotu Tian, Zhaoxia Wang
Exploration of the Common Gene Characteristics and Molecular Mechanism of Parkinson's Disease and Crohn's Disease from Transcriptome Data. Brain sciences 12 (6) (2022)
Xiaochen Han, Feixia Zhan, Yuxin Yao, Zhaoxia Wang, Jianguo Liu, Sheng Yao
Clinical heterogeneity in a family with flail arm syndrome and review of hnRNPA1-related spectrum. Annals of clinical and translational neurology (2022)
Xiya Shen, Jiawei Zhang, Feixia Zhan, Wotu Tian, Qingqing Jiang, Xinghua Luan, Xiaojie Zhang, Zhaoxia Wang
Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in <i>HSPB1</i> Gene: A Case Series. Biomolecules 12 (10) (2022)
Wo-Tu Tian, Fei-Xia Zhan, Zhen-Hua Liu, Zhe Liu, Qing Liu, Xia-Nan Guo, Zai-Wei Zhou, Shi-Ge Wang, Xiao-Rong Liu, Jiang Hong, Xun-Hua Li, Guo-Hua Zhao, Hai-Yan Li, Jian-Guang Tang, Guang-Hui Bi, Ping Zhong, Xiao-Meng Yin, Tao-Tao Liu, Rui-Long Ni, Hao-Ran Zheng, Xiao-Li Liu, Xiao-Hang Qian, Jing-Ying Wu, Yu-Wen Cao, Chao Zhang, Shi-Hua Liu, Ying-Ying Wu, Qun-Feng Wang, Ting Xu, Wen-Zhe Hou, Zi-Yi Li, Hui-Yi Ke, Ze-Yu Zhu, Lan Zheng, Tian Wang, Tian-Yi Rong, Li Wu, Yu Zhang, Kan Fang, Zhan-Hang Wang, Ya-Kun Zhang, Mei Zhang, Yu-Wu Zhao, Bei-Sha Tang, Xing-Hua Luan, Xiao-Jun Huang, Zhaoxia Wang
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large-Sample Study. Movement disorders : official journal of the Movement Disorder Society (2021)
Zhaoxia Wang, Xiaojun Huang, Ning Wang, Zhiying Wu, Cheng Zhang, Weihong Gu, Shuyan Cong, Jianhua Ma, Ling Wei, Yanchun Deng, Qi Fang, Qi Niu, Jin Wang, Zhaoxia Wang, You Yin, Jinyong Tian, Shufen Tian, Hongyan Bi, Hong Jiang, Xiaorong Liu, Yang Lü, Meizhen Sun, Jianjun Wu, Erhe Xu, Tao Chen, Tao Chen, Xu Chen, Wei Li, Shujian Li, Qinghua Li, Xiaonan Song, Ying Tang, Ping Yang, Yun Yang, Min Zhang, Xiong Zhang, Yuhu Zhang, Ruxu Zhang, Yi Ouyang, Jintai Yu, Quanzhong Hu, Qing Ke, Yuanrong Yao, Zhe Zhao, Xiuhe Zhao, Guohua Zhao, Furu Liang, Nan Cheng, Jianhong Han, Rong Peng, Shengdi Chen, Beisha Tang
Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China. Translational neurodegeneration 10 (1) (2021)
Feixia Zhan, Xiaoli Liu, Ruilong Ni, Taotao Liu, Yuwen Cao, Jingying Wu, Wotu Tian, Xinghua Luan, Zhaoxia Wang
Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome. Metabolic brain disease (2021)
Fei-Xia Zhan, Ze-Yu Zhu, Qing Liu, Hai-Yan Zhou, Xing-Hua Luan, Xiao-Jun Huang, Xiao-Li Liu, Wo-Tu Tian, Shi-Ge Wang, Xiao-Xuan Song, Guang Chen, Ming-Liang Zhao, Ying Wang, Hui-Dong Tang, Jiong Hu, Sheng-Di Chen, Bin-Yin Li, Zhaoxia Wang
Altered structural and functional connectivity in CSF1R-related leukoencephalopathy. Brain imaging and behavior 15 (3) (2021)
Fei-Xia Zhan, Zhaoxia Wang
Late-onset autoimmune polyendocrine syndrome type 1: a case report and literature review. Immunologic research 69 (2) (2021)
Fei-Xia Zhan, Shi-Ge Wang, Zhaoxia Wang
Advances in hyperekplexia and other startle syndromes. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 42 (10) (2021)
Jianwen Deng, Jianwen Deng, Xueyu Guo, Jingli Shan, Xinghua Luan, Li Cao, Juan Zhao, Meng Yu, Wei Zhang, He Lv, Zhiying Xie, LingChao Meng, Yiming Zheng, Yawen Zhao, Qiang Gang, Qingqing Wang, Jing Liu, Min Zhu, Binbin Zhou, Pidong Li, Yinzhe Liu, Yang Wang, Chuanzhu Yan, Daojun Hong, Yun Yuan, Zhaoxia Wang
The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3. Brain : a journal of neurology 144 (6) (2021)
Yuwen Cao, Jingying Wu, Yunhua Yue, Chao Zhang, Shihua Liu, Ping Zhong, Shige Wang, Xiaojun Huang, Weiping Deng, Jing Pan, Lan Zheng, Qing Liu, Liang Shang, Benyan Zhang, Jie Yang, Guang Chen, Shufen Chen, Zhaoxia Wang, Xinghua Luan
Expanding the clinical spectrum of adult-onset neuronal intranuclear inclusion disease. Acta neurologica Belgica (2021)
Jiaxi Yu, Xing-Hua Luan, Meng Yu, Wei Zhang, He Lv, Zhaoxia Wang, Lingchao Meng, Min Zhu, Binbin Zhou, Xiao-Rong Wu, Pidong Li, Qiang Gang, Jing Liu, Xin Shi, Wei Liang, Zhirong Jia, Sheng Yao, Yun Yuan, Jianwen Deng, Dao-Jun Hong, Zhaoxia Wang
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy. Annals of clinical and translational neurology 8 (6) (2021)
Wo-Tu Tian, Li-Hua Liu, Hai-Yan Zhou, Chao Zhang, Fei-Xia Zhan, Ze-Yu Zhu, Sheng-Di Chen, Xing-Hua Luan, Zhaoxia Wang
New phenotype of DCTN1-related spectrum: early-onset dHMN plus congenital foot deformity. Annals of clinical and translational neurology 7 (2) (2020)
Wo-Tu Tian, Hai-Yan Zhou, Fei-Xia Zhan, Ze-Yu Zhu, Jie Yang, Sheng-Di Chen, Xing-Hua Luan, Zhaoxia Wang
Lysosomal degradation of GMPPB is associated with limb-girdle muscular dystrophy type 2T. Annals of clinical and translational neurology 6 (6) (2019)
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, Zhaoxia Wang
Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy. Translational neurodegeneration 8 (2019)

Zhaoxia Wang.css-eqlu8i{font-size:small;padding-left:4px;} (Li Cao)

Publication Activity (10 Years)

Top Topics

Top Venues

Zhaoxia Wang (Li Cao)