Anemia following zinc treatment for Wilson’s disease: a case report and literature review

por Cai, Sha, Gong, Jing-Yu, Yang, Jing, Wang, Jian-She
Publicado 2019

Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid

por Zhang, Mei-Hong, Knisely, A. S., Wang, Neng-li, Gong, Jing-Yu, Wang, Jian-She
Publicado 2016

UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation

por Abuduxikuer, Kuerbanjiang, Fang, Ling-Juan, Li, Li-Ting, Gong, Jing-Yu, Wang, Jian-She
Publicado 2018

Recurrent acute liver failure associated with novel SCYL1 mutation: A case report

por Li, Jia-Qi, Gong, Jing-Yu, Knisely, A S, Zhang, Mei-Hong, Wang, Jian-She
Publicado 2019

Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomes

por Zhang, Mei-Hong, Setchell, Kenneth DR, Zhao, Jing, Gong, Jing-Yu, Lu, Yi, Wang, Jian-She
Publicado 2019

Successful treatment of infantile oxysterol 7α-hydroxylase deficiency with oral chenodeoxycholic acid

por Tang, Yun-Ping, Gong, Jing-Yu, Setchell, Kenneth D. R., Zhang, Wujuan, Zhao, Jing, Wang, Jian-She
Publicado 2021

The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency

por Wang, Neng-Li, Li, Li-Ting, Wu, Bing-Bing, Gong, Jing-Yu, Abuduxikuer, Kuerbanjiang, Li, Gang, Wang, Jian-She
Publicado 2016

Novel NBAS mutations and fever-related recurrent acute liver failure in Chinese children: a retrospective study

por Li, Jia-Qi, Qiu, Yi-Ling, Gong, Jing-Yu, Dou, Li-Min, Lu, Yi, Knisely, A. S., Zhang, Mei-Hong, Luan, Wei-Sha, Wang, Jian-She
Publicado 2017

A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions

por Wang, Neng-Li, Lu, Yu-Lan, Zhang, Ping, Zhang, Mei-Hong, Gong, Jing-Yu, Lu, Yi, Xie, Xin-Bao, Qiu, Yi-Ling, Yan, Yan-Yan, Wu, Bing-bing, Wang, Jian-She
Publicado 2016

Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ‐glutamyltransferase cholestasis

por Qiu, Yi‐Ling, Gong, Jing‐Yu, Feng, Jia‐Yan, Wang, Ren‐Xue, Han, Jun, Liu, Teng, Lu, Yi, Li, Li‐Ting, Zhang, Mei‐Hong, Sheps, Jonathan A., Wang, Neng‐Li, Yan, Yan‐Yan, Li, Jia‐Qi, Chen, Lian, Borchers, Christoph H., Sipos, Bence, Knisely, A.S., Ling, Victor, Xing, Qing‐He, Wang, Jian‐She
Publicado 2017