| 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] |
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| 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) doi: 10.1016/j.jceh.2026.103555
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| 2 |
Maria Amendola, Lara Berklite, Simon Horslen, James E. Squires. Genetic and Familial Forms of Pediatric Intrahepatic Cholestasis. Clinics in Liver Disease 2026; doi: 10.1016/j.cld.2026.07.002
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| 3 |
Ali Islek, Serap Ketenci İşlek, Gokhan Tumgor. Progressive familial intrahepatic cholestasis: From childhood to adulthood. World Journal of Gastroenterology 2026; 32(41): 121544 doi: 10.3748/wjg.121544
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| 4 |
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 Literature. Journal of Clinical and Experimental Hepatology 2026; 16(2) doi: 10.1016/j.jceh.2025.103418
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| 5 |
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 disease. World Journal of Hepatology 2025; 17(10): 109770 doi: 10.4254/wjh.v17.i10.109770
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| 6 |
Richa Gupta, Rodrigo M. Florentino, Amala Alenchery, Lara E. Berklite, James E. Squires. Molecular Mechanisms of Progressive Familial Intrahepatic Cholestasis. Seminars in Liver Disease 2026; doi: 10.1055/a-2933-3012
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| 7 |
Yuji Jiang, Weiyuan Fang, Mingzi Cen, Jihu Li, Jianshe Wang, Jinxi Ding, Ye Chen. The disease burden and health-related quality of life in Chinese children with genetic cholestatic liver diseases: a cross-sectional study of progressive familial intrahepatic cholestasis and Alagille syndrome. Orphanet Journal of Rare Diseases 2026; 21(1) doi: 10.1186/s13023-026-04365-8
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| 8 |
Zhe Zhou, Sven C. D. van IJzendoorn. MYO5B Deficiency-Associated Cholestasis and the Role of the Bile Salt Export Pump. Cells 2026; 15(1) doi: 10.3390/cells15010092
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| 9 |
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 regulation. Journal of Ethnopharmacology 2026; 366 doi: 10.1016/j.jep.2026.121639
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| 10 |
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 cases. Frontiers in Pediatrics 2026; 14 doi: 10.3389/fped.2026.1843435
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| 11 |
Eliza Flanagan, Natassia Pinpin Tan. Genetic Cholestasis Syndromes. Clinics in Liver Disease 2026; 30(3) doi: 10.1016/j.cld.2026.04.005
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