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Cited by in CrossRef
For: Mkarem LE, Batika MAH, Bitar R. New hope in treating progressive familial intrahepatic cholestasis in children. World J Hepatol 2025; 17(7): 108253 [PMID: 40747224 DOI: 10.4254/wjh.v17.i7.108253]
URL: https://www.wjgnet.com/1948-5182/full/v17/i7/108253.htm
Number Citing Articles
1
Somashekara H. Ramakrishna, Keerthivasan Seetharaman, M.R. Acharya, Prasanna Gopal, Anbarasu Karthik, Nataraj Palaniappan, Karthik N. Ramaswamy, Mettu S. Reddy. Living Donor Liver Transplantation for Progressive Familial Intrahepatic Cholestasis Type 13 (PFIC 13)Journal of Clinical and Experimental Hepatology 2026; 16(4): 103555 doi: 10.1016/j.jceh.2026.103555
2
Rohan Grotra, Prasenjit Das, Rajni Yadav, Lalita Mehra, Ashok Tiwari, Rohan Malik. Bortezomib Therapy in Autoimmune-BSEP Disease After Liver Transplantation: Case Report With Review of the LiteratureJournal of Clinical and Experimental Hepatology 2026; 16(2): 103418 doi: 10.1016/j.jceh.2025.103418
3
Yuan Chen, Zhi-Yi Wang, Bao-Qi Chen, Yu-Juan Qi, Hai-Yan Liu, Wen-Xin Shi, Lu Guo, Zhi Liu, Li-Feng Sun. Clinical characteristics and genetic causes of unexplained pediatric liver diseaseWorld Journal of Hepatology 2025; 17(10): 109770 doi: 10.4254/wjh.v17.i10.109770
4
Zhe Zhou, Sven C. D. van IJzendoorn. MYO5B Deficiency-Associated Cholestasis and the Role of the Bile Salt Export PumpCells 2026; 15(1): 92 doi: 10.3390/cells15010092
5
Huiru Liu, Songsong Wang, Na Wang, Fang Wang, Jin Ren, Zirong Zhou, Kairui Liu, Xinyan Wang, Yubo Li, Chunsheng Fu, Liwen Han. Mechanisms and key active ingredients of HeDan capsules in ameliorating MASLD via bile acid metabolism regulationJournal of Ethnopharmacology 2026; 366: 121639 doi: 10.1016/j.jep.2026.121639
6
Yun-Ping Tang, Xu-Xia Wei, Ning Xue, Hai-Ying Yang, Hua Li. Etiology and clinical characteristics of infantile cholestasis: a single-center retrospective study of 326 casesFrontiers in Pediatrics 2026; 14 doi: 10.3389/fped.2026.1843435
7
Eliza Flanagan, Natassia Pinpin Tan. Genetic Cholestasis SyndromesClinics in Liver Disease 2026;  doi: 10.1016/j.cld.2026.04.005