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Chinese Medical Journal|February 21, 2012
A new frame-shifting mutation of UGT1A1 gene causes type I Crigler-Najjar syndromeJin Wang, Ling-Juan Fang, Long Li, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|May 22, 2020
An infant presenting with extreme hypertriglyceridemia diagnosed as glycogen storage disease type IaLing-Juan Fang, Kuerbanjiang Abuduxikuer, Xiu-Mei Yan, et al.Medicine|December 15, 2018
UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlationKuerbanjiang Abuduxikuer, Ling-Juan Fang, Li-Ting Li, 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.Journal of Pediatric Gastroenterology and Nutrition|February 21, 2012
Chinese children with chronic intrahepatic cholestasis and high γ-glutamyl transpeptidase: clinical features and association with ABCB4 mutationsLing-Juan Fang, Xiao-Hong Wang, A S Knisely, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|August 10, 2013
[Mutation analysis of FAH gene in patients with tyrosinemia type 1]Li-Min Dou, Ling-Juan Fang, Xiao-Hong Wang, et al.World Journal of Gastroenterology|November 1, 2012
Biochemical characteristics of neonatal cholestasis induced by citrin deficiencyJian-She Wang, Xiao-Hong Wang, Ying-Jie Zheng, et al.Microbial Pathogenesis|June 8, 2020
1H NMR-based metabolomics analyses in children with Helicobacter pylori infection and the alteration of serum metabolites after treatmentLing-Juan Fang, Xiao-Chun Lin, Dian Huang, et al.Pageof 1