Identification of Hub Genes and Biological Pathways in Inclusion Body Myositis Using Bioinformatics Analysis

por Wu, Yue, Zhao, Zijun, Zhang, Jinru, Wang, Yaye, Song, Xueqin
Publicado 2022

MORC2 p.R252W Mutant Axonal Charcot–Marie–Tooth Disease Causes Peripheral Neuropathies and Pathological Myofiber Destruction

por Wang, Yaye, Han, Jingzhe, Zhang, Jinru, Wu, Yue, Song, Xueqin
Publicado 2022

Case report: Meningoencephalocele and recurrent bacterial meningitis in chronic idiopathic intracranial hypertension

por Zhang, Jinru, Wu, Jianchao, Wu, Yue, Wang, Yaye, Han, Jingzhe
Publicado 2022

A family with riboflavin-reactive lipid deposition myopathy caused by a novel compound heterozygous mutation in the electron transfer flavoprotein dehydrogenase gene

por Wu, Yue, Han, Jingzhe, Wang, Yaye, Zhang, Jinru, Song, Xueqin, Ji, Guang
Publicado 2020

A case of reversible splenial lesion syndrome secondary to Fanconi syndrome with white matter swelling as the main manifestation

por Han, Jingzhe, Wang, Yaye, Wu, Yue, Zhang, Jinru, Song, Xueqin, Ji, Guang
Publicado 2021

Formation of chlorate and perchlorate during electrochemical oxidation by Magnéli phase Ti(4)O(7) anode: inhibitory effects of coexisting constituents

por Wang, Lu, Wang, Yaye, Sui, Yufei, Lu, Junhe, Hu, Baowei, Huang, Qingguo
Publicado 2022

A novel splice‐site mutation in CHMP2B associated with frontotemporal dementia: The first report from China and literature review

por Li, Chang, Wen, Ya, Zhao, Mengqiu, Wang, Yaye, Li, Ping, Wang, Liang, Wang, Shan
Publicado 2023

A novel compound heterozygous SPG7 variant is associated with progressive spastic ataxia and persecutory delusions found in Chinese patients: two case reports

por Wang, Shan, Wang, Yaye, Wu, Yue, Zhang, Jinru, Zhang, Weilin, Li, Chang, Song, Xueqin
Publicado 2022

Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency

por Zhang, Jinru, Han, Jingzhe, Wang, Yaye, Wu, Yue, Ma, Lixia, Song, Xueqin, Ji, Guang
Publicado 2022

Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal–Distal Myopathy in a Chinese Patient

por Ji, Guang, Wang, Ning, Han, Xu, Wang, Yaye, Zhang, Jinru, Wu, Yue, Wu, Hongran, Ma, Shaojuan, Song, Xueqin
Publicado 2022