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Browsing by Author Wang, Zhaoxia
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Showing results 1 to 20 of 102
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Issue Date
Title
Author(s)
2017
Adult-onset demyelinating neuropathy associated with FBLN5 gene mutation
Cheng, Si
;
Lv, He
;
Zhang, Wei
;
Wang, Zhaoxia
;
Shi, Xin
;
Liang, Wei
;
Yuan, Yun
2019
Appendicular skeletal muscle mass: A more sensitive biomarker of disease severity than BMI in adults with mitochondrial diseases
Hou, Yue
;
Xie, Zhiying
;
Zhao, Xutong
;
Yuan, Yun
;
Dou, Pan
;
Wang, Zhaoxia
2011
Asian patients with limb girdle muscular dystrophy 21 (LGMD21)
Hong, Daojun
;
Zhang, Wei
;
Wang, Wei
;
Wang, Zhaoxia
;
Yuan, Yun
2010
Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene
Hong, Daojun
;
Luan, Xinghua
;
Chen, Bin
;
Zheng, Riliang
;
Zhang, Wei
;
Wang, Zhaoxia
;
Yuan, Yun
23-Dec-2021
Cerebral large artery occlusion in chronic graft-versus-host disease A case report
Li, Ying
;
Gao, Feng
;
Sun, Wei
;
Wang, Zhaoxia
;
Jin, Haiqiang
2022
Cerebrospinal Fluid sTREM2 Has Paradoxical Association with Brain Structural Damage Rate in Early- and Late-Stage Alzheimer's Disease
Leng, Fangda
;
Zhan, Zhenying
;
Sun, Yunchuang
;
Liu, Fang
;
Edison, Paul
;
Sun, Yongan
;
Wang, Zhaoxia
2007
Cerebrotendinous xanthomatosis with a compound heterozygote mutation and severe polyneuropathy
Wang, Zhaoxia
;
Yuan, Yun
;
Zhang, Wei
;
Zhang, Ying
;
Feng, Liqun
25-Dec-2020
CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations
Ogasawara, Masashi
;
Iida, Aritoshi
;
Kumutpongpanich, Theerawat
;
Ozaki, Ayami
;
Oya, Yasushi
;
Konishi, Hirofumi
;
Nakamura, Akinori
;
Abe, Ryuta
;
Takai, Hiroshi
;
Hanajima, Ritsuko
;
Doi, Hiroshi
;
Tanaka, Fumiaki
;
Nakamura, Hisayoshi
;
Nonaka, Ikuya
;
Wang, Zhaoxia
;
Hayashi, Shinichiro
;
Noguchi, Satoru
;
Nishino, Ichizo
2019
Characteristics of Pompe disease in China: a report from the Pompe registry
Zhao, Yuying
;
Wang, Zhaoxia
;
Lu, Jiahong
;
Gu, Xuefan
;
Huang, Yonglan
;
Qiu, Zhengqing
;
Wei, Yanping
;
Yan, Chuanzhu
2013
Chronic progressive external ophthalmoplegia coexistent with motor neuron disease in a patient with a novel large-scale mitochondrial DNA deletion
Zhao, Danhua
;
Wang, Zhaoxia
;
Hong, Daojun
;
Zhang, Wei
;
Yuan, Yun
2009
Clincial and pathological study of distal motor neuropathy with N88S mutation in BSCL2
Chen, Bin
;
Zheng, Riliang
;
Luan, Xinghua
;
Zhang, Wei
;
Wang, Zhaoxia
;
Yuan, Yun
2014
Clinical and GAA gene mutation analysis in mainland Chinese patients with late-onset Pompe disease: identifying c.2238G > C as the most common mutation
Liu, Xiao
;
Wang, Zhaoxia
;
Jin, Weina
;
Lv, He
;
Zhang, Wei
;
Que, Chengli
;
Huang, Yu
;
Yuan, Yun
2019
Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients
Xie, Zhiying
;
Hou, Yue
;
Yu, Meng
;
Liu, Yilin
;
Fan, Yanbin
;
Zhang, Wei
;
Wang, Zhaoxia
;
Xiong, Hui
;
Yuan, Yun
2015
Clinical and Muscle Imaging Findings in 14 Mainland Chinese Patients with Oculopharyngodistal Myopathy
Zhao, Juan
;
Liu, Jing
;
Xiao, Jiangxi
;
Du, Jing
;
Que, Chengli
;
Shi, Xin
;
Liang, Wei
;
Sun, Weiping
;
Zhang, Wei
;
Lv, He
;
Yuan, Yun
;
Wang, Zhaoxia
Jun-2020
Clinical and pathological features in adult-onset NIID patients with cortical enhancement
Liang, Huiting
;
Wang, Bo
;
Li, Qing
;
Deng, Jianwen
;
Wang, Lulu
;
Wang, Huan
;
Li, Xiaobin
;
Zhu, Min
;
Cai, Yu
;
Wang, Zhaoxia
;
Yuan, Yun
;
Fang, Pu
;
Hong, Daojun
2017
Clinical and Pathological Variation of Charcot-Marie-Tooth 1A in a Large Chinese Cohort
Wu, Rui
;
Lv, He
;
Zhang, Wei
;
Wang, Zhaoxia
;
Zuo, Yuehuan
;
Liu, Jing
;
Yuan, Yun
9-Dec-2020
Clinical features and genotypes of Laing distal myopathy in a group of Chinese patients, with in-frame deletions of MYH7 as common mutations
Yu, Meng
;
Zhu, Ying
;
Lu, Yuanyuan
;
Lv, He
;
Zhang, Wei
;
Yuan, Yun
;
Wang, Zhaoxia
2010
CLINICAL PHENOTYPE OF AUTOSOMAL DOMINANT PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA IN A FAMILY WITH A NOVEL MUTATION IN THE C10orf2 GENE
Hong, Daojun
;
Bi, Hongyan
;
Yao, Sheng
;
Wang, Zhaoxia
;
Yuan, Yun
May-2021
Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients
Fan, Yanbin
;
Tan, Dandan
;
Song, Danyu
;
Zhang, Xu
;
Chang, Xingzhi
;
Wang, Zhaoxia
;
Zhang, Cheng
;
Chan, Sophelia Hoi-Shan
;
Wu, Qixi
;
Wu, Liwen
;
Wang, Shuang
;
Yan, Hui
;
Ge, Lin
;
Yang, Haipo
;
Mao, Bing
;
Boennemann, Carsten
;
Liu, Jingying
;
Wang, Suxia
;
Yuan, Yun
;
Wu, Xiru
;
Zhang, Hong
;
Xiong, Hui
29-Jan-2020
Cognitive Profile of Patients With Mitochondrial Chronic Progressive External Ophthalmoplegia
Zhang, Guanyu
;
Hou, Yue
;
Wang, Zhaoxia
;
Ye, Zheng
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