Zhaoxia Wang

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 24

Top Topics

Myasthenia Gravis

End Stage Renal Disease

Muscular Dystrophy

Top Venues

Annals of clinical and translational neurology

Orphanet journal of rare diseases

Journal of medical genetics

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

Publications

Yalan Wan, Chao Zhou, Xingzhi Chang, Liwen Wu, Yilei Zheng, Jiaxi Yu, Li Bai, Mingyue Luan, Meng Yu, Qi Wang, Wei Zhang, Yun Yuan, Jianwen Deng, Zhaoxia Wang
Novel TUBA4A variant causes congenital myopathy with focal myofibrillar disorganisation. Journal of medical genetics 61 (7) (2024)
Xutong Zhao, Meng Yu, Wei Zhang, Yue Hou, Yun Yuan, Zhaoxia Wang
Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study. Orphanet journal of rare diseases 19 (1) (2024)
Yang Zhao, Xutong Zhao, Kunqian Ji, Junling Wang, Yuying Zhao, Jie Lin, Qiang Gang, Meng Yu, Yun Yuan, Haishan Jiang, Chong Sun, Fang Fang, Chuanzhu Yan, Zhaoxia Wang
The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross-sectional study. Clinical genetics (2024)
Yalan Wan, Chao Zhou, Xingzhi Chang, Liwen Wu, Yilei Zheng, Jiaxi Yu, Li Bai, Mingyue Luan, Meng Yu, Qi Wang, Wei Zhang, Yun Yuan, Jianwen Deng, Zhaoxia Wang
Novel TUBA4A variant causes congenital myopathy with focal myofibrillar disorganisation. Journal of medical genetics (2024)
Yalan Wan, Chao Zhou, Xingzhi Chang, Liwen Wu, Yilei Zheng, Jiaxi Yu, Li Bai, Mingyue Luan, Meng Yu, Qi Wang, Wei Zhang, Yun Yuan, Jianwen Deng, Zhaoxia Wang
Novel TUBA4A variant causes congenital myopathy with focal myofibrillar disorganisation. Journal of medical genetics 61 (7) (2024)
Zhihao Xie, Chang Liu, Chengyue Sun, Yilin Liu, Jieru Peng, Lingchao Meng, Jianwen Deng, Zhaoxia Wang, Chunxia Yang, Yun Yuan, Zhiying Xie
Single-Nucleus RNA Sequencing Unravels Early Mechanisms of Human Becker Muscular Dystrophy. Annals of neurology (2024)
Xutong Zhao, Meng Yu, Wei Zhang, Yue Hou, Yun Yuan, Zhaoxia Wang
Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study. Orphanet journal of rare diseases 19 (1) (2024)
Xutong Zhao, Meng Yu, Wei Zhang, Yue Hou, Yun Yuan, Zhaoxia Wang
Demographic characteristics, diagnostic challenges, treatment patterns, and caregiver burden of mitochondrial diseases: a retrospective cross-sectional study. Orphanet journal of rare diseases 19 (1) (2024)
Yuwei Tang, Jing Liu, Feng Gao, Hongjun Hao, Zhirong Jia, Wei Zhang, Xin Shi, Wei Liang, Meng Yu, He Lv, Ying Tan, Zhiying Li, Yu Wang, Yun Yuan, Lingchao Meng, Zhaoxia Wang
CIDP/autoimmune nodopathies with nephropathy: a case series study. Annals of clinical and translational neurology (2023)
Yikang Wang, Yawen Zhao, Meng Yu, Luhua Wei, Wei Zhang, Zhaoxia Wang, Yun Yuan
Clinicopathological and circulating cell-free DNA profile in myositis associated with anti-mitochondrial antibody. Annals of clinical and translational neurology (2023)
Yang Zhao, Yue Hou, Xutong Zhao, Tongling Liufu, Meng Yu, Wei Zhang, Zhiying Xie, Victor Wei Zhang, Yun Yuan, Zhaoxia Wang
The clinical, myopathological, and genetic analysis of 155 Chinese mitochondrial ophthalmoplegia patients with mitochondrial DNA single large deletions. Molecular genetics & genomic medicine (2023)
Wenhao Zhang, Yiming Zheng, Yikang Wang, Hui Xiong, Chengli Que, Xiaohui Zhang, Ying Zhu, Yawen Zhao, Meng Yu, Lingchao Meng, He Lv, Wei Zhang, Hongjun Hao, Jiangxi Xiao, Yun Yuan, Zhaoxia Wang
Thigh MRI in antisynthetase syndrome, and comparisons with dermatomyositis and immune-mediated necrotising myopathy. Rheumatology (Oxford, England) (2022)
Qi Wang, Meng Yu, Wei Zhang, Qiang Gang, Zhiying Xie, Jin Xu, Chao Zhou, Depeng Wang, Lingchao Meng, He Lv, Zhirong Jia, Jianwen Deng, Yun Yuan, Zhaoxia Wang
Subsarcolemmal and cytoplasmic p62 positivity and rimmed vacuoles are distinctive for PLIN4-myopathy. Annals of clinical and translational neurology 9 (11) (2022)
Kang Du, Xujun Chu, Yuwei Tang, Xutong Zhao, Meng Yu, Yiming Zheng, Jianwen Deng, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Lingchao Meng
Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics. Annals of clinical and translational neurology 9 (7) (2022)
Yawen Zhao, Ying Li, Yang Bian, Sheng Yao, Penju Liu, Meng Yu, Wei Zhang, Zhaoxia Wang, Yun Yuan
Congenital myasthenic syndrome in China: genetic and myopathological characterization. Annals of clinical and translational neurology 8 (4) (2021)
Qiang Gang, Conceição Bettencourt, Stefen Brady, Janice L Holton, Estelle G Healy, John McConville, Patrick J Morrison, Michela Ripolone, Raffaella Violano, Monica Sciacco, Maurizio Moggio, Marina Mora, Renato Mantegazza, Simona Zanotti, Zhaoxia Wang, Yun Yuan, Wei-Wei Liu, David Beeson, Michael Hanna, Henry Houlden
Genetic defects are common in myopathies with tubular aggregates. Annals of clinical and translational neurology 9 (1) (2021)
Kang Du, Fan Li, Hui Wang, Yuanfeng Miao, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Lingchao Meng
Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study. Annals of clinical and translational neurology 8 (4) (2021)
Qi Wang, Meng Yu, Zhiying Xie, Jing Liu, Qingqing Wang, He Lv, Wei Zhang, Yun Yuan, Zhaoxia Wang
Mutational and clinical spectrum of centronuclear myopathy in 9 cases and a literature review of Chinese patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (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)
Meng Yu, Ying Zhu, Yuanyuan Lu, He Lv, Wei Zhang, Yun Yuan, Zhaoxia Wang
Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations. Orphanet journal of rare diseases 15 (1) (2020)
Yue Hou, Zhiying Xie, Xutong Zhao, Yun Yuan, Pan Dou, Zhaoxia Wang
Appendicular skeletal muscle mass: A more sensitive biomarker of disease severity than BMI in adults with mitochondrial diseases. PloS one 14 (7) (2019)
Zhiying Xie, Jiangxi Xiao, Yiming Zheng, Zhaoxia Wang, Yun Yuan
Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the FKRP Gene. BioMed research international 2018 (2018)
Rui Wu, He Lv, Wei Zhang, Zhaoxia Wang, Yuehuan Zuo, Jing Liu, Yun Yuan
Clinical and Pathological Variation of Charcot-Marie-Tooth 1A in a Large Chinese Cohort. BioMed research international 2017 (2017)
Meng Yu, Yiming Zheng, Suqin Jin, Qiang Gang, Qingqing Wang, Peng Yu, He Lv, Wei Zhang, Yun Yuan, Zhaoxia Wang
Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing. PloS one 12 (4) (2017)