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 |
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
|
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): 1438 doi: 10.18621/eurj.1340536
|
3 |
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; doi: 10.1097/LVT.0000000000000351
|
4 |
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
|
5 |
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: 1 doi: 10.1155/2023/1960152
|
6 |
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): 319 doi: 10.1146/annurev-pathmechdis-031521-025623
|
7 |
Javier Martínez-García, Angie Molina, Gloria González-Aseguinolaza, Nicholas D. Weber, Cristian Smerdou. Gene Therapy for Acquired and Genetic Cholestasis. Biomedicines 2022; 10(6): 1238 doi: 10.3390/biomedicines10061238
|
8 |
Alvin P. Chan, Robert S. Venick. Childhood Cholestatic Liver Diseases that Persist Into Adulthood. Journal of Clinical Gastroenterology 2023; 57(7): 686 doi: 10.1097/MCG.0000000000001850
|
9 |
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; doi: 10.1002/biof.2041
|
10 |
Moinak Sen Sarma, Aathira Ravindranath. Pediatric acute viral hepatitis with atypical variants: Clinical dilemmas and natural history. World Journal of Hepatology 2022; 14(5): 945 doi: 10.4254/wjh.v14.i5.945
|
11 |
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
|
12 |
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
|
13 |
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): 4684 doi: 10.3390/jcm11164684
|
14 |
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
|