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For: Alam S, Lal BB. Recent updates on progressive familial intrahepatic cholestasis types 1, 2 and 3: Outcome and therapeutic strategies. World J Hepatol 2022; 14(1): 98-118 [PMID: 35126842 DOI: 10.4254/wjh.v14.i1.98]
URL: https://www.wjgnet.com/1948-5182/full/v14/i1/98.htm
Number Citing Articles
1
Roman A. Gudkov, Andrey V. Dmitriyev, Natal'ya V. Fedina, Valeriya I. Petrova, Tat'yana A. Teryokhina, Alina E. Sologub. Differential Diagnosis of Conjugated Hyperbilirubinemia in Infancy (Literature Review). I.P. Pavlov Russian Medical Biological Herald 2024; 32(2) doi: 10.17816/PAVLOVJ188846
2
Ali Topak. Next-generation sequencing panel test results in pediatric patients with progressive familial intrahepatic cholestasis: a single-center experience. The European Research Journal 2023; 9(6) doi: 10.18621/eurj.1340536
3
Sarah Cayton, Lindsay C. Czuba. Altered Bile Acid Transport in Liver Disease. Biomedicines 2026; 14(5) doi: 10.3390/biomedicines14051037
4
Amal Abdmouleh, Houweyda Jilani, Imen Rejeb, Syrine Hizem, Nicolas Pottier, Romain Larrue, Wendy Arondal, Lucie Hanquet, Rania Benrabeh, Olfa Bouyahia, Sonia Mazigh, Yasmina Elaribi, Lamia Benjemaa. Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next‐Generation Sequencing: Case Series of 70 Patients. Clinical Genetics 2026;  doi: 10.1111/cge.70242
5
Guillermo Alejandro Costaguta, Fernando Álvarez. Pediatric cirrhosis: special consideration for its diagnosis and management. Exploration of Digestive Diseases 2025; 4 doi: 10.37349/edd.2025.1005104
6
Xiyan Ding, Jiaming Wang, Yicui Wang, Huaming Xu, Yanxin Liu. Therapeutic modulation of the gut microbiota by traditional Chinese medicine in the management of cholestatic liver injury. Frontiers in Cellular and Infection Microbiology 2026; 16 doi: 10.3389/fcimb.2026.1807162
7
Jagadeesh Menon, Naresh Shanmugam, Mukul Vij, Fadl H. Veerankutty, Ashwin Rammohan, Mohamed Rela. Simultaneous total internal biliary diversion during liver transplantation for progressive familial intrahepatic cholestasis type 1: Standard of care?. Liver Transplantation 2024; 30(7) doi: 10.1097/LVT.0000000000000351
8
Javier Martínez-García, Angie Molina, Gloria González-Aseguinolaza, Nicholas D. Weber, Cristian Smerdou. Gene Therapy for Acquired and Genetic Cholestasis. Biomedicines 2022; 10(6) doi: 10.3390/biomedicines10061238
9
Mohamed Abdelmalak Abokandil, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdelhady, Mohamed Mansy, Mostafa Kotb. Progressive familial intrahepatic cholestasis type 4: a case report. Journal of Medical Case Reports 2024; 18(1) doi: 10.1186/s13256-024-04662-5
10
Irene Blázquez-García, Laura Guerrero, Mary Dayne S. Tai, Américo Cerqueira, Ana Cuervo, Alberto Paradela, Fernando J. Corrales. Decoding the Cellular Response to Methylthioadenosine Uncovers Novel Targets for Chronic Liver Disease. Cells 2026; 15(19) doi: 10.3390/cells15191720
11
Manal Abdel Gawad, Aml Mahfouz, Mona Abdel-Hadi, Heba Mastor, Basant Elbanna. Novel genetic variants and atypical phenotypes in pediatric progressive familial intrahepatic cholestasis. Pediatric Research 2026;  doi: 10.1038/s41390-026-05422-5
12
T. N. Belkova, E. B. Pavlinova, K. B. Kurieva, Yu. E. Golovanova, A. Yu. Konstantinova, A. Kh. Begjanova. A case report of progressive familial intrahepatic cholestasis in neonatal practice. Meditsinskiy sovet = Medical Council 2024; (11) doi: 10.21518/ms2024-216
13
Simon P Horslen, Georg Vogel, Jolan Terner-Rosenthal, Nadav Zadok, Lorenzo D'Antiga. Progressive familial intrahepatic cholestasis disease burden and clinical approaches: a systematic review. Journal of Comparative Effectiveness Research 2026;  doi: 10.57264/cer-2026-0047
14
Israa Sharabati, Ruaa Mustafa Qafesha, Mohamed M.M. Mustafa, Mahmoud Diaa Hindawi, Heba Rasras, Sami Bannoura, Mohammed Abdulrazzak, Ibrahim Shamasneh. Novel ABCB4 mutation in a female patient with progressive familial intrahepatic cholestasis type 3: a case report and literature review. Annals of Medicine & Surgery 2025; 87(2) doi: 10.1097/MS9.0000000000002813
15
Noor Hasmee, Sangam Kumari, Hema Joshi, Saman Naseema, Bhupendra Singh, Vinod Arora. Navigating the complexities of progressive familial intrahepatic cholestasis-II: Genetic insights, patient outcomes, and nursing implications – A case report. Journal of Pediatric Nursing 2026; 89 doi: 10.1016/j.pedn.2026.05.001
16
Arun Ajmera MD, Justin Baba MD, Mohammad Salimian MD, Samuel Hwang MD, Aditi Dagli MD, Akash Pandey MD. Reevaluating cholestasis: a case of PFIC3 diagnosed through whole genome sequencing after initial miss on cholestasis genetic panel. Gastroenterology & Hepatology: Open access 2024; 15(3) doi: 10.15406/ghoa.2024.15.00582
17
Yosra Riahi, Marion Almes, Manon Banet, Elodie Mareux, Isabelle Garcin, Anne Davit-Spraul, Redouane Si-Bouazza, Sylvie Fabrega, Benjamin Boucherle, Jean-Luc Decout, Thomas Falguières, Isabelle Callebaut, Emmanuel Jacquemin, Emmanuel Gonzales, Martine Lapalus. Contrasting impacts of two ABCB11 variants affecting the same residue in progressive familial intrahepatic cholestasis type 2. American Journal of Physiology-Gastrointestinal and Liver Physiology 2026; 331(3) doi: 10.1152/ajpgi.00055.2026
18
Moinak Sen Sarma, Aathira Ravindranath. Pediatric acute viral hepatitis with atypical variants: Clinical dilemmas and natural history. World Journal of Hepatology 2022; 14(5): 944-955 doi: 10.4254/wjh.v14.i5.944
19
Rachit Bansal, Abhay Patel, Chinmaya Singh, Kiran N C, Sonakshi Saxena. Recurrent Jaundice Unraveled: A Case of Benign Recurrent Intrahepatic Cholestasis (BRIC) in an Indian Patient. Cureus 2024;  doi: 10.7759/cureus.74736
20
Chenyue Hang, Yijie Jin, Yi Luo, Mingxuan Feng, Tao Zhou, Jianjun Zhu, Jianjun Zhang, Yuan Liu, Qiang Xia. Long-Term Results of Pediatric Liver Transplantation for Progressive Familial Intrahepatic Cholestasis. Journal of Clinical Medicine 2022; 11(16) doi: 10.3390/jcm11164684
21
Badriah G Alasmari, Syed Rayees, Mohammed Alomari, Lina Elzubair, Yassin Hamid. Progressive Familial Intrahepatic Cholestasis Type 3 Homozygous Pathogenic Variant c.2906G>A in the ATP Binding Cassette Subfamily B Member 4 (ABCB4) Gene: A Case Report of an Unusual Presentation. Cureus 2022;  doi: 10.7759/cureus.32455
22
Leilei Yu, Yaru Liu, Shunhe Wang, Qingsong Zhang, Jianxin Zhao, Hao Zhang, Arjan Narbad, Fengwei Tian, Qixiao Zhai, Wei Chen. Cholestasis: exploring the triangular relationship of gut microbiota-bile acid-cholestasis and the potential probiotic strategies. Gut Microbes 2023; 15(1) doi: 10.1080/19490976.2023.2181930
23
Njood Alwadei. A Hematologic Masquerader: Progressive Familial Intrahepatic Cholestasis Type 3 Presenting as Anemia, Hepatosplenomegaly, and Recurrent Bleeding in a Child. Clinical Case Reports 2026; 14(6) doi: 10.1002/ccr3.72961
24
Anu K. Vasudevan, Naresh Shanmugam, Ashwin Rammohan, Joseph J. Valamparampil, Kshetra Rinaldhy, Jagadeesh Menon, Ravikumar Thambithurai, Saravanapandian Namasivayam, Ilankumaran Kaliamoorthy, Mohamed Rela. Outcomes of pediatric liver transplantation for progressive familial intrahepatic cholestasis. Pediatric Transplantation 2023; 27(8) doi: 10.1111/petr.14600
25
Fahad I. Alsohaibani, Musthafa C. Peedikayil, Abdulaziz F. Alfadley, Mohamed K. Aboueissa, Faisal A. Abaalkhail, Saleh A. Alqahtani, Dirk Uhlmann. Progressive Familial Intrahepatic Cholestasis: A Descriptive Study in a Tertiary Care Center. International Journal of Hepatology 2023; 2023 doi: 10.1155/2023/1960152
26
Harry Sutton, Saul J. Karpen, Binita M. Kamath. Pediatric Cholestatic Diseases: Common and Unique Pathogenic Mechanisms. Annual Review of Pathology: Mechanisms of Disease 2024; 19(1) doi: 10.1146/annurev-pathmechdis-031521-025623
27
Rubaiyat Alam. Atypical presentation of pediatric acute hepatitis A: Is the situation alarming?. World Journal of Virology 2025; 14(4): 114174 doi: 10.5501/wjv.v14.i4.114174
28
Alvin P. Chan, Robert S. Venick. Childhood Cholestatic Liver Diseases that Persist Into Adulthood. Journal of Clinical Gastroenterology 2023; 57(7) doi: 10.1097/MCG.0000000000001850
29
Sophia Heinrich, Annika Behrendt, Malte Sgodda, Holger Gohlke, Bernd Auber, Amelie Stalke, Björn Hartleben, Heiner Wedemeyer, Tobias Cantz, Richard Taubert. Functional inactivation of MDR3 caused by a homozygous ABCB4 missense variant leading to liver failure. Frontiers in Genetics 2026; 17 doi: 10.3389/fgene.2026.1802238
30
R.A. GUDKOV, A.V. DMITRIEV, N.V. FEDINA, V.I. PETROVA. PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS IN CHILDREN. AVICENNA BULLETIN 2024; 27(1) doi: 10.25005/2074-0581-2025-27-1-143-154
31
Laura Guerrero, Lorena Carmona‐Rodríguez, Fátima Milhano Santos, Sergio Ciordia, Luiz Stark, Loreto Hierro, Pablo Pérez‐Montero, David Vicent, Fernando J. Corrales. Molecular basis of progressive familial intrahepatic cholestasis 3. A proteomics study. BioFactors 2024; 50(4) doi: 10.1002/biof.2041
32
Angelo Di Giorgio, Marco Sciveres, Maurizio Fuoti, PierLuigi Calvo, Mara Cananzi, Ana Lleo, Simona Gatti, Giuseppe Indolfi, Annalisa Madeo, Claudia Mandato, Federica Nuti, Chiara Zanchi, Greta Carioli, Arianna Ghirardi, Emanuele Nicastro, Lorenzo D’Antiga. Real-world experience with odevixibat in children with progressive familial intrahepatic cholestasis. JHEP Reports 2025; 7(4) doi: 10.1016/j.jhepr.2024.101309
33
Chiara Simoni, Justine Nozi, Francesco Starinieri, Tiziana La Bella, Elisabetta Manta, Camilla Negri, Mauro Biffi, Rossana Norata, Martina Rocchi, Francesca Sanvito, Giuseppe Ronzitti, Elena Barbon, Alessio Cantore. Liver fibrosis negatively impacts in vivo gene transfer to murine hepatocytes. Nature Communications 2025; 16(1) doi: 10.1038/s41467-025-57383-8
34
Huma Arshad Cheema, Aliaksandr Skrahin, Anjum Saeed, Zafar Fayyaz, Muhammad Arshad Alvi, Muhammad Nadeem Anjum, Nadia Waheed, Khalil Ur Rehman, Ahmad Malik, Volha Skrahina, Arndt Rolfs. Clinical Diversity and Outcomes of Progressive Familial Intrahepatic Cholestasis Diagnosed by Whole Genome Sequencing in Pakistani Children. GenoMed Connect 2025; 1(1) doi: 10.69709/GenomC.2025.165225
35
S. Ya. Volgina, N. A. Solovieva, G. A. Kulakova, E. A. Kurmaeva, A. I. Mukhamadieva, R. R. Shaydullina. Genetic and phenotypic features familial intrahepatic cholestasis: case report. Experimental and Clinical Gastroenterology 2026; (1) doi: 10.31146/1682-8658-ecg-245-1-143-152
36
Angelo Di Giorgio, Marco Sciveres, Maurizio Fuoti, PierLuigi Calvo, Mara Cananzi, Ana Lleo, Simona Gatti, Giuseppe Indolfi, Annalisa Madeo, Claudia Mandato, Federica Nuti, Chiara Zanchi, Greta Carioli, Arianna Ghirardi, Emanuele Nicastro, Lorenzo D’Antiga. Early predictors of pruritus response in children with PFIC treated with odevixibat. Digestive and Liver Disease 2026;  doi: 10.1016/j.dld.2026.08.036
37
Moinak Sen Sarma, Aathira Ravindranath. Pediatric acute viral hepatitis with atypical variants: Clinical dilemmas and natural history. World Journal of Hepatology 2022; 14(5) doi: 10.4254/wjh.v14.i5.945
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38
Fernando Gil-Lopez, Lydia A. Mercado, Nicole M. Loo. Remarkable Response to Odevixibat in an Adult With Progressive Familial Intrahepatic Cholestasis Type 1 and Intractable Pruritus. ACG Case Reports Journal 2026; 13(3) doi: 10.14309/crj.0000000000002033
39
Rong Chen, Feng-Xia Yang, Yan-Fang Tan, Mei Deng, Hua Li, Yi Xu, Wen-Xian Ouyang, Yuan-Zong Song. Clinical and genetic characterization of pediatric patients with progressive familial intrahepatic cholestasis type 3 (PFIC3): identification of 14 novel ABCB4 variants and review of the literatures. Orphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-022-02597-y
40
Vikram Bains, Deepak Joshi. An overview of paediatric autoimmune and genetic cholestatic liver disease for the adult physician. Clinical Medicine 2025; 25(6) doi: 10.1016/j.clinme.2025.100533
41
Guy Lacey, Toby Gosden, Oliver Darlington, Elise Evers, Robin Howard, Lucia Quadrado. Indirect Comparison of Maralixibat and Odevixibat for the Treatment of Progressive Familial Intrahepatic Cholestasis. Clinical Therapeutics 2025; 47(11) doi: 10.1016/j.clinthera.2025.05.011
42
Ashutosh Prince, C. Alicia Traughber, Yavar Shiravand, Nilam Bhandari, Mariam R Khan, Swati Sharma, Kara Timinski, Karen F Murray, Laura N. Bull, Kailash Gulshan. Enigmatic functions of ATP8B1: cholestasis, inflammation, phosphoinositide flipping, and cellular homeostasis. Cell Cycle 2025; 24(21-24) doi: 10.1080/15384101.2025.2574275