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Journal of Pediatric Gastroenterology and Nutrition|September 23, 2017
Severe Neonatal Cholestasis in Cerebrotendinous Xanthomatosis: Genetics, Immunostaining, Mass SpectrometryJing-Yu Gong, Kenneth D R Setchell, Jing Zhao, et al.World Journal of Clinical Cases|May 18, 2021
Pediatric Wilson disease presenting as acute liver failure: Prognostic indicesWei-Yuan Fang, Kuerbanjiang Abuduxikuer, Peng Shi, et al.Biomolecules & Biomedicine|February 24, 2024
JAM3: A prognostic biomarker for bladder cancer via epithelial-mesenchymal transition regulationZhong-Qi Pang, Jian-She Wang, Jin-Feng Wang, et al.Journal of Medical Genetics|May 30, 2024
ZFYVE19 deficiency: a ciliopathy involving failure of cell division, with cell deathJing Yang, Ya-Nan Zhang, Ren-Xue Wang, et al.Human Mutation|November 8, 2019
TJP2 hepatobiliary disorders: Novel variants and clinical diversityJing Zhang, Lang-Li Liu, Jing-Yu Gong, et al.BMC Medical Genetics|January 12, 2011
Clinical and molecular characterization of Wilson's disease in China: identification of 14 novel mutationsXin-Hua Li, Yi Lu, Yun Ling, et al.World Journal of Pediatrics : WJP|January 19, 2023
Poly-hydroxylated bile acids and their prognostic roles in Alagille syndromeMeng-Xuan Wang, Jun Han, Teng Liu, et al.Journal of Medical Genetics|August 2, 2020
Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasisWeisha Luan, Chen-Zhi Hao, Jia-Qi Li, et al.Clinical Genetics|March 30, 2024
Kinesin family member 12-related hepatopathy: A generally indolent disorder with elevated gamma-glutamyl-transferase activityGeorg-Friedrich Vogel, Alexandra Podpeskar, Dietmar Rieder, et al.Hepatology (Baltimore, Md.)|August 19, 2025
A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasisJian Ding, Hui-Yu She, Ye Cheng, et al.Pageof 13