Peripheral Nervous System Involvement in Late-Onset Cobalamin C Disease?

por Chu, Xujun, Meng, Lingchao, Zhang, Wei, Luo, Jinjun, Wang, Zhaoxia, Yuan, Yun
Publicado 2020

TTR Gly83Arg Mutation: Beyond Familial Vitreous Amyloidosis

por Li, Zhenxian, Du, Kang, Chu, Xujun, Lv, He, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun, Meng, Lingchao
Publicado 2022

Vagus nerve ultrasound in transthyretin familial amyloid polyneuropathy: A pilot study

por Du, Kang, Xu, Ke, Chu, Xujun, Tang, Yuwei, Lv, He, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun, Meng, Lingchao
Publicado 2021

Skeletal Muscle Involvement Pattern of Hereditary Transthyretin Amyloidosis: A Study Based on Muscle MRI

por Chu, Xujun, Du, Kang, Tang, Yuwei, Zhao, Xutong, Yu, Meng, Zheng, Yiming, Deng, Jianwen, Lv, He, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun, Meng, Lingchao
Publicado 2022

Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics

por Du, Kang, Chu, Xujun, Tang, Yuwei, Zhao, Xutong, Yu, Meng, Zheng, Yiming, Deng, Jianwen, Lv, He, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun, Meng, Lingchao
Publicado 2022

First Identification of Rare Exonic and Deep Intronic Splice-Altering Variants in Patients With Beta-Sarcoglycanopathy

por Xie, Zhiying, Sun, Chengyue, Liu, Chang, Chu, Xujun, Gang, Qiang, Yu, Meng, Zheng, Yiming, Meng, Lingchao, Li, Fan, Xia, Dongliang, Wang, Li, Li, Ying, Deng, Jianwen, Lv, He, Wang, Zhaoxia, Zhang, Wei, Yuan, Yun
Publicado 2022

Clinical and biochemical characterization of hereditary transthyretin amyloidosis caused by E61K mutation

por Chu, Xujun, Wang, Mengdie, Tang, Ran, Huang, Yanan, Yu, Jiaxi, Cao, Yunfeng, Zheng, Yilei, Xie, Zhiying, Deng, Jianwen, Wang, Zhi, Ma, Wei, Song, Wenjing, Wu, Yuan, Lv, He, Zhang, Wei, Wang, Zhaoxia, Yuan, Yun, Liu, Yu, Meng, Lingchao
Publicado 2022