Advances in diagnosis and treatment of limb-girdle muscular dystrophy

by Meng YU, Zhao-xia WANG
Published 2017-08-01

Diagnosis and Management of Kearns-Sayre Syndrome Rely on Comprehensive Clinical Evaluation

by Meng Yu, Lei Yu, Zhao-Xia Wang
Published 2016-01-01

The hazardous effects of tobacco smoking on male fertility

by Jing-Bo Dai, Zhao-Xia Wang, Zhong-Dong Qiao
Published 2015-01-01

Clinical and imaging differences between limb⁃girdle muscular dystrophy type 2B and immune⁃mediated necrotizing myopathy

by Ya⁃wen ZHAO, Yan⁃li WANG, Zhao⁃xia WANG, Wei ZHANG, Yun YUAN
Published 2020-09-01

Muscle Magnetic Resonance Imaging for the Differentiation of Multiple Acyl-CoA Dehydrogenase Deficiency and Immune-mediated Necrotizing Myopathy

by Ya-Wen Zhao, Xiu-Juan Liu, Wei Zhang, Zhao-Xia Wang, Yun Yuan
Published 2018-01-01

Hereditary Transthyretin Amyloidosis in Eight Chinese Families

by Ling-Chao Meng, He Lyu, Wei Zhang, Jing Liu, Zhao-Xia Wang, Yun Yuan
Published 2015-01-01

Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with Dysferlinopathy

by Su-Qin Jin, Meng Yu, Wei Zhang, He Lyu, Yun Yuan, Zhao-Xia Wang
Published 2016-01-01

Optical coherence tomography findings in chronic progressive external ophthalmoplegia

by Yuan Wu, Lei Kang, Hai-Long Wu, Yue Hou, Zhao-Xia Wang, Yuan-Yuan Ji
Published 2019-05-01

Compound Heterozygote Mutation of C12orf65 Causes Distal Motor Neuropathy and Optic Atrophy

by Xiao-Jing Fang, Wei Zhang, He Lyu, Zhao-Xia Wang, Wei-Wei Wang, Yun Yuan
Published 2017-01-01

Effect of Cognitive Function on Balance and Posture Control after Stroke

by Hui-xian Yu, Zhao-xia Wang, Chang-bin Liu, Pei Dai, Yue Lan, Guang-qing Xu
Published 2021-01-01

Clinical and gene mutation analysis on Alexander's disease type Ⅱ caused by a novel GFAP mutation

by Yun-chuang SUN, Yi-ning HUANG, Hui ZHU, Hai-qiang JIN, Fan LI, Zhao-xia WANG
Published 2019-03-01

The m.3243A > G mutation load in hair follicles from different scalp regions of patients with MELAS

by Yuan-yuan LU, Xu-tong ZHAO, Qing-qing WANG, Xiao ZHANG, Yun YUAN, Zhao-xia WANG
Published 2018-08-01

Whole-Exome Sequencing Identified a Novel Homozygous Frameshift Mutation of HPS3 in a Consanguineous Family with Hermansky-Pudlak Syndrome

by Zhao-Xia Wang, Yi-Hui Liu, Yi Dong, Ya-Li Li, Tie-Yu Tang, Liang-Liang Fan
Published 2021-01-01

Study of Enhanced Depth Imaging Optical Coherence Tomography in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

by Xiao-Jing Fang, Meng Yu, Yuan Wu, Zi-Hao Zhang, Wei-Wei Wang, Zhao-Xia Wang, Yun Yuan
Published 2017-01-01

Clinical analysis on two patients with N-hexane toxic peripheral neuropathy misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy

by Yi LI, Ling-chao MENG, He LÜ, Wei ZHANG, Zhao-xia WANG, Jing LIU, Yue-huan ZUO, Yun YUAN
Published 2019-06-01

Analysis on clinical features of necrotizing autoimmune myopathy

by Yi LI, Jun FU, Ling-chao MENG, Wei ZHANG, Zhao-xia WANG, He LÜ, Yue-huan ZUO, Yun YUAN
Published 2016-10-01

Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease

by Yuan-Yuan Lu, He Lyu, Su-Qin Jin, Yue-Huan Zuo, Jing Liu, Zhao-Xia Wang, Wei Zhang, Yun Yuan
Published 2017-01-01

Clinical features of the late ⁃ onset mitochondrial encephalomyopathy with lactic acidosis and stroke⁃like episodes

by Dan⁃hua ZHAO, Xu⁃tong ZHAO, Hai⁃ying XING, Xiao ZHANG, Zhe ZHANG, Xian⁃zeng LIU, Yun YUAN, Zhao⁃xia WANG
Published 2020-03-01

Value of serum muscle enzymes in the differential diagnosis of myopathies

by Yuan-yuan MA, Meng YU, Xiao-fang LI, Zhi-ying XIE, Xue-ying LI, Zhe ZHANG, Yun YUAN, Zhao-xia WANG
Published 2019-05-01

Clinical study of respiratory function in patients with late-onset glycogen storage disease typeⅡ

by Wei-na JIN, Cheng-li QUE, Hai-yan TANG, Yu HUANG, Zhao-xia WANG, Xiao LIU, He LÜ, Wei ZHANG, Yun YUAN
Published 2014-05-01