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For: Vinayagamoorthy V, Srivastava A, Sarma MS. Newer variants of progressive familial intrahepatic cholestasis. World J Hepatol 2021; 13(12): 2024-2038 [PMID: 35070006 DOI: 10.4254/wjh.v13.i12.2024]
URL: https://www.wjgnet.com/1007-9327/full/v13/i12/2024.htm
Number Citing Articles
1
Angela Pepe, Angelo Colucci, Martina Carucci, Lucia Nazzaro, Cristina Bucci, Giusy Ranucci, Angelo Di Giorgio, Pietro Vajro, Claudia Mandato. Case Report: Add-on treatment with odevixibat in a new subtype of progressive familial intrahepatic cholestasis broadens the therapeutic horizon of genetic cholestasisFrontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1061535
2
Hana Halabi, Khawla Kalantan, Warif Abdulhaq, Habeib Alshaibi, Mohammed A Almatrafi. A Rare Case of Progressive Familial Intrahepatic Cholestasis Type 4: A Case Report and Literature ReviewCureus 2023;  doi: 10.7759/cureus.47276
3
Bikrant Bihari Lal, Seema Alam, Anupam Sibal, Karunesh Kumar, Somashekara Hosaagrahara Ramakrishna, Vaibhav Shah, Nirmala Dheivamani, Ashish Bavdekar, Aabha Nagral, Nishant Wadhwa, Arjun Maria, Aashay Shah, Ira Shah, Zahabiya Nalwalla, Pandey Snehavardhan, K.P. Srikanth, Subhash Gupta, Viswanathan M. Sivaramakrishnan, Yogesh Waikar, Arya Suchismita, A. Ashritha, Vikrant Sood, Rajeev Khanna. Genotype correlates with clinical course and outcome of children with tight junction protein 2 (TJP2) deficiency–related cholestasisHepatology 2024; 80(3): 511 doi: 10.1097/HEP.0000000000000828
4
Mahintaj Dara, Negar Azarpira, Nasrin Motazedian, Mahdokht Hossein-Aghdaie, Seyed-Mohsen Dehghani, Bita Geramizadeh, Elaheh Esfandiari. Expression of miR-let7b and miR-19b in progressive familial intrahepatic cholestasis (PFIC) childrenGastroenterología y Hepatología (English Edition) 2024; 47(1): 24 doi: 10.1016/j.gastre.2023.03.003
5
Angelo Di Giorgio, Marco Sciveres, Maurizio Fuoti, Aurelio Sonzogni, Claudia Mandato, Lorenzo D'Antiga. Treatment with an ileal bile acid transporter inhibitor in patients with TJP2 deficiencyClinics and Research in Hepatology and Gastroenterology 2023; 47(8): 102185 doi: 10.1016/j.clinre.2023.102185
6
Vipul Gautam, Kalpana Panda, Vikram Kumar, Shaleen Agarwal, Subhash Gupta. Youngest Living Donor Liver Transplant for End‐Stage Liver Disease in a 6‐Month‐Old With a Novel Aggressive Mutation in KIF12 GenePediatric Transplantation 2024; 28(5) doi: 10.1111/petr.14804
7
Mohamed Abdelmalak Abokandil, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdelhady, Mohamed Mansy, Mostafa Kotb. Progressive familial intrahepatic cholestasis type 4: a case reportJournal of Medical Case Reports 2024; 18(1) doi: 10.1186/s13256-024-04662-5
8
K. S. Nezhdanov, E. N. Shirokova, Yu. O. Shulpekova, A. S. Ostrovskaya, M. S. Zharkova, V. T. Ivashkin. A 19-year-old Patient with Recurrent Pruritus and JaundiceRussian Journal of Gastroenterology, Hepatology, Coloproctology 2023; 33(3): 66 doi: 10.22416/1382-4376-2023-33-3-66-75
9
Muhammad Imran, Ahmed Bostamy Elsnhory, Ahmed A. Ibrahim, Mohamed Elnaggar, Muhammad Shammas Tariq, Areeba Mariam Mehmood, Shujaat Ali, Saba Khalil, Sheharyar Hassan Khan, Mansab Ali, Mohamed Abuelazm. Efficacy and Safety of Ileal Bile Acid Transport Inhibitors in Inherited Cholestatic Liver Disorders: A Meta-analysis of Randomized Controlled Trials.Journal of Clinical and Experimental Hepatology 2024; : 102462 doi: 10.1016/j.jceh.2024.102462
10
Dalal Ben Sabbahia, Meriem Atrasssi, Nissrine Bennani, Abdelhakim Benmoussa, Abdelhak Abkari. ZFYVE19 gene mutation: A novel variant of progressive familial intrahepatic cholestasisJPGN Reports 2024;  doi: 10.1002/jpr3.12111
11
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 strategiesGut Microbes 2023; 15(1) doi: 10.1080/19490976.2023.2181930
12
Yue Zu, Yanan Liu, Lulu Lan, Chen Zhu, Chengliang Zhang, Dong Liu. Consecutive baicalin treatment relieves its accumulation in rats with intrahepatic cholestasis by increasing MRP2 expressionHeliyon 2023; 9(1): e12689 doi: 10.1016/j.heliyon.2022.e12689
13
Maria Noelle Hüpper, Judith Pichler, Wolf-Dietrich Huber, Andreas Heilos, Rebecca Schaup, Martin Metzelder, Sophie Langer. Surgical versus Medical Management of Progressive Familial Intrahepatic Cholestasis—Case Compilation and Review of the LiteratureChildren 2023; 10(6): 949 doi: 10.3390/children10060949
14
Mahintaj Dara, Negar Azarpira, Nasrin Motazedian, Mahdokht Hossein-Aghdaie, Seyed-Mohsen Dehghani, Bita Geramizadeh, Elaheh Esfandiari. Expression of miR-let7b and miR-19b in progressive familial intrahepatic cholestasis (PFIC) childrenGastroenterología y Hepatología 2024; 47(1): 24 doi: 10.1016/j.gastrohep.2023.03.001
15
Rachel M. Golonka, Beng San Yeoh, Piu Saha, Amira Gohara, Ramakumar Tummala, Stanislaw Stepkowski, Amit K. Tiwari, Bina Joe, Frank J. Gonzalez, Andrew T. Gewirtz, Matam Vijay-Kumar. Loss of toll-like receptor 5 potentiates spontaneous hepatocarcinogenesis in farnesoid X receptor–deficient miceHepatology Communications 2023; 7(6) doi: 10.1097/HC9.0000000000000166
16
Ikuo Tomioka, Chihiro Ota, Yuka Tanahashi, Kayoko Ikegami, Ayaka Ishihara, Nanami Kohri, Hiroshi Fujii, Kanako Morohaku. Loss of the DNA-binding domain of the farnesoid X receptor gene causes severe liver and kidney injuriesBiochemical and Biophysical Research Communications 2024; 721: 150125 doi: 10.1016/j.bbrc.2024.150125
17
Harry Sutton, Saul J. Karpen, Binita M. Kamath. Pediatric Cholestatic Diseases: Common and Unique Pathogenic MechanismsAnnual Review of Pathology: Mechanisms of Disease 2024; 19(1): 319 doi: 10.1146/annurev-pathmechdis-031521-025623
18
Coşkun Fırat Özkeçeci, Melike Arslan, Edibe Gözde Başaran, Yasin Maruf Ergen, Önder Bozdoğan, Necati Balamtekin. Non-syndromic perspective on a unique progressive familial intrahepatic cholestasis variant: <i>ZFYVE19 </i>mutationThe Turkish Journal of Pediatrics 2024; 66(4): 505 doi: 10.24953/turkjpediatr.2024.4655
19
Deanna M. Bowman, Izumi Kaji, James R. Goldenring. Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular LevelCellular and Molecular Gastroenterology and Hepatology 2022; 14(3): 553 doi: 10.1016/j.jcmgh.2022.04.015
20
Tingting Lv, Jidong Jia. Rare liver diseases are not rare in ChinaLiver International 2022; 42(9): 2023 doi: 10.1111/liv.15267
21
Nicole Heinz, Jennifer Vittorio. Treatment of Cholestasis in Infants and Young ChildrenCurrent Gastroenterology Reports 2023; 25(11): 344 doi: 10.1007/s11894-023-00891-8
22
Binbin Liu, Jie Zhang, Lu Shao, Jiaming Yao, Shuli Yang. San-Huang-Chai-Zhu Formula Ameliorates Liver Injury in Intrahepatic Cholestasis through Suppressing SIRT1/PGC-1α-Regulated Mitochondrial Oxidative StressEvidence-Based Complementary and Alternative Medicine 2022; 2022: 1 doi: 10.1155/2022/7832540
23
Chiao‐Yu Yang, Hung‐Wen Tsai, Yen‐Yin Chou, Yao‐Jong Yang. NR1H4 mutation and rapid progressive intrahepatic cholestasis in infancy: A case report and literature reviewClinical Case Reports 2024; 12(2) doi: 10.1002/ccr3.8531
24
Arghya Samanta, Neha Parveen, Moinak Sen Sarma, Ujjal Poddar, Anshu Srivastava. Cholestatic Liver Disease due to Novel USP53 Mutations: A Case Series of Three Indian ChildrenJournal of Clinical and Experimental Hepatology 2024; 14(2): 101290 doi: 10.1016/j.jceh.2023.10.001
25
Joanna Głowska-Ciemny, Marcin Szymanski, Agata Kuszerska, Rafał Rzepka, Constantin S. von Kaisenberg, Rafał Kocyłowski. Role of Alpha-Fetoprotein (AFP) in Diagnosing Childhood Cancers and Genetic-Related Chronic DiseasesCancers 2023; 15(17): 4302 doi: 10.3390/cancers15174302
26
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 practiceMeditsinskiy sovet = Medical Council 2024; (11): 306 doi: 10.21518/ms2024-216
27
Guillaume Morcrette, Monique Fabre. Biopsie hépatique dans la prise en charge des cholestases de l’enfantRevue Francophone des Laboratoires 2023; 2022(548): 60 doi: 10.1016/S1773-035X(22)00405-1
28
Dr Moinak Sen Sarma, Chiranjit Gope. Approach to a Sick Neonate with Cholestasis in IndiaAnnals of Pediatric Gastroenterology & Hepatology 2022; 4(2): 6 doi: 10.5005/jp-journals-11009-0094