A case report: Co-occurrence of Wilson disease and oculocutaneous albinism in a Chinese patient

por Rao, Rao, Shu, Shan, Han, Yong Zhu, Chiu, Yu-Jen, Han, Yong Sheng
Publicado 2018

Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report

por Wang, Juan, Wu, Jun-Cang, Yu, Xu-En, Han, Yong-Zhu, Yang, Ren-Min
Publicado 2018

The study of Wilson disease in pregnancy management

por Yu, Xu-En, Pan, Min, Han, Yong-Zhu, Yang, Ren-Min, Wang, Juan, Gao, Shan
Publicado 2019

Characteristics of neurological Wilson’s disease with corpus callosum abnormalities

por Zhou, Zhi-Hua, Wu, Yun-Fan, Cao, Jin, Hu, Ji-Yuan, Han, Yong-Zhu, Hong, Ming-Fan, Wang, Gong-Qiang, Liu, Shu-Hu, Wang, Xue-Min
Publicado 2019

Case report: A Chinese patient with spinocerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation

por Chen, Lin, Xu, Yin, Fang, Ming-juan, Shi, Yong-guang, Zhang, Jie, Zhang, Liang-liang, Wang, Yu, Han, Yong-zhu, Hu, Ji-yuan, Yang, Ren-min, Yu, Xu-en
Publicado 2023

A weighted cranial diffusion-weighted imaging scale for Wilson’s disease

por Wang, Shi-jing, Geng, Hao, Cheng, Si-rui, Xu, Chen-chen, Zhang, Rui-qi, Wang, Yu, Wu, Tong, Li, Bo, Wang, Tao, Han, Yong-sheng, Ding, Zeng-hui, Sun, Yi-ning, Wang, Xun, Han, Yong-zhu, Cheng, Nan
Publicado 2023