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World Journal of Gastroenterology|February 28, 2019
Δ4-3-oxosteroid-5β-reductase deficiency: Responses to oral bile acid therapy and long-term outcomesMei-Hong Zhang, Kenneth Dr Setchell, Jing Zhao, et al.Journal of Gastroenterology|October 8, 2010
The mutation spectrum of the SLC25A13 gene in Chinese infants with intrahepatic cholestasis and aminoacidemiaHai-Yan Fu, Shao-Ren Zhang, Xiao-Hong Wang, et al.Frontiers in Endocrinology|June 28, 2019
Novel Melanocortin 2 Receptor Variant in a Chinese Infant With Familial Glucocorticoid Deficiency Type 1, Case Report and Review of LiteratureKuerbanjiang Abuduxikuer, Zhong-Die Li, Xin-Bao Xie, et al.Frontiers in Pediatrics|February 23, 2023
Neonatal sclerosing cholangitis with novel mutations in DCDC2 (doublecortin domain-containing protein 2) in Chinese childrenXia Wei, Yuan Fang, Jian-She Wang, et al.World Journal of Gastroenterology|May 12, 2010
Most common SLC25A13 mutation in 400 Chinese infants with intrahepatic cholestasisHai-Yan Fu, Shao-Ren Zhang, Hui Yu, et al.World Journal of Pediatrics : WJP|December 24, 2008
Clinical and pathological characteristics of Alagille syndrome in Chinese childrenJian-She Wang, Xiao-Hong Wang, Qi-Rong Zhu, et al.Human Mutation|April 14, 2025
Balanced Translocation Disrupting JAG1 Identified by Optical Genomic Mapping in Suspected Alagille SyndromeYi-Qiong Zhang, Peng-Fei Gao, Jing-Min Yang, et al.Frontiers in Genetics|April 4, 2022
The Presence of Vacuolated Kupffer Cells Raises a Clinical Suspicion of Niemann-Pick Disease Type C in Neonatal CholestasisNeng-Li Wang, Lian Chen, Yi Lu, et al.World Journal of Gastroenterology|January 17, 2013
Primary ∆4-3-oxosteroid 5β-reductase deficiency: two cases in ChinaJing Zhao, Ling-Juan Fang, Kenneth D R Setchell, et al.BMC Gastroenterology|April 14, 2021
Successful treatment of infantile oxysterol 7α-hydroxylase deficiency with oral chenodeoxycholic acidYun-Ping Tang, Jing-Yu Gong, Kenneth D R Setchell, et al.Pageof 13