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 en Medicine (Baltimore) (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 en Medicine (Baltimore) (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 en BMC Pregnancy Childbirth (2019)

Comparative study of biliary trace elements and clinical phenotypes in Wilson’s disease

por Ren, Ming-Shan, Fan, Yu-Xin, Yang, Ren-Min, Han, Yong-Zhu, Wu, Guo-Jun, Xin, Yu-Rong, Yu, Long
Publicado en World J Gastroenterol (1997)

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 en BMC Neurol (2019)