Limb-girdle Muscular Dystrophy Type 2A with Muscular Eosinophilic Infiltration in a Chinese Patient

por Luo, Yue-Bei, Li, Qiu-Xiang, Duan, Hui-Qian, Bi, Fang-Fang, Yang, Huan
Publicado 2018

Clinicopathological‐genetic features of congenital myasthenic syndrome from a Chinese neuromuscular centre

por Huang, Kun, Duan, Hui‐Qian, Li, Qiu‐Xiang, Luo, Yue‐Bei, Bi, Fang‐Fang, Yang, Huan
Publicado 2022

Expanding the clinicopathological-genetic spectrum of glycogen storage disease type IXd by a Chinese neuromuscular center

por Huang, Kun, Duan, Hui-Qian, Li, Qiu-Xiang, Luo, Yue-Bei, Bi, Fang-Fang, Yang, Huan
Publicado 2022

Expanding the clinicopathological‐genetic spectrum of GNE myopathy by a Chinese neuromuscular centre

por Zhang, Kai‐Yue, Duan, Hui‐Qian, Li, Qiu‐Xiang, Luo, Yue‐Bei, Bi, Fang‐Fang, Huang, Kun, Yang, Huan
Publicado 2021

CASQ1‐related myopathy: The first report from China and the literature review

por Zhang, Kai‐Yue, Zhang, Geng‐Jian, Duan, Hui‐Qian, Li, Qiu‐Xiang, Huang, Kun, Xu, Li‐Qun, Yang, Huan, Luo, Yue‐Bei
Publicado 2022

Calcitriol increases MBNL1 expression and alleviates myotonic dystrophy phenotypes in HSA(LR) mouse models

por Huang, Kun, Wang, Dan-Dan, Hu, Wen-Bao, Zeng, Wei-Qian, Xu, Xia, Li, Qiu-Xiang, Bi, Fang-Fang, Yang, Huan, Qiu, Jian
Publicado 2022