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For: van der Woerd WL, Houwen RH, van de Graaf SF. Current and future therapies for inherited cholestatic liver diseases. World J Gastroenterol 2017; 23(5): 763-775 [PMID: 28223721 DOI: 10.3748/wjg.v23.i5.763]
URL: https://www.wjgnet.com/1007-9327/full/v23/i5/763.htm
Number Citing Articles
1
Hao Bing, Yi-Ling Li, Dan Li, Chen Zhang, Bing Chang. Case Report: A Rare Heterozygous ATP8B1 Mutation in a BRIC1 Patient: Haploinsufficiency?Frontiers in Medicine 2022; 9 doi: 10.3389/fmed.2022.897108
2
Naser-Aldin Lashgari, Danial Khayatan, Nazanin Momeni Roudsari, Saeideh Momtaz, Ahmad Reza Dehpour, Amir Hossein Abdolghaffari. Therapeutic approaches for cholestatic liver diseases: the role of nitric oxide pathwayNaunyn-Schmiedeberg's Archives of Pharmacology 2024; 397(3): 1433 doi: 10.1007/s00210-023-02684-2
3
Beatriz Mínguez Rodríguez, Cristina Molera Busoms, Loreto Martorell Sampol, Ruth García Romero, Gemma Colomé Rivero, Javier Martín de Carpi. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohortGastroenterología y Hepatología 2022; 45(8): 585 doi: 10.1016/j.gastrohep.2021.12.005
4
Yi-Gui Zou, Huan Wang, Wen-Wen Li, Dong-Ling Dai. Challenges in pediatric inherited/metabolic liver disease: Focus on the disease spectrum, diagnosis and management of relatively common disordersWorld Journal of Gastroenterology 2023; 29(14): 2114-2126 doi: 10.3748/wjg.v29.i14.2114
5
Alastair Baker, Nanda Kerkar, Lora Todorova, Binita M. Kamath, Roderick H.J. Houwen. Systematic review of progressive familial intrahepatic cholestasisClinics and Research in Hepatology and Gastroenterology 2019; 43(1): 20 doi: 10.1016/j.clinre.2018.07.010
6
H. Eickhölter, C. Krüger, S. Kathemann, M. Endmann. Die intrahepatische, familiäre Cholestase – Manifestation bei einer Jugendlichen mit Pruritus und Ikterus nach Beginn oraler KontrazeptionMonatsschrift Kinderheilkunde 2023;  doi: 10.1007/s00112-023-01806-7
7
Eva Sticova, Milan Jirsa, Joanna Pawłowska. New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical ImplicationsCanadian Journal of Gastroenterology and Hepatology 2018; 2018: 1 doi: 10.1155/2018/2313675
8
Wenkang Gao, Zhonglin Li, Huikuan Chu, Hang Yuan, Lilin Hu, Lin Yao, Li Zhang, Weijun Wang, Rong Lin, Ling Yang. Pharmacotherapy for Liver Cirrhosis and Its Complications2022; : 81 doi: 10.1007/978-981-19-2615-0_6
9
Christoph Slavetinsky, Ekkehard Sturm. Odevixibat and partial external biliary diversion showed equal improvement of cholestasis in a patient with progressive familial intrahepatic cholestasisBMJ Case Reports 2020; 13(6): e234185 doi: 10.1136/bcr-2019-234185
10
Saigopala Reddy, Nathan Fleishman, Katherine Dempsey, Edwin Ferren, Michal Kamionek, Vani V. Gopalareddy. Progressive Familial Intrahepatic Cholestasis-2 Mimicking Non-accidental InjuryACG Case Reports Journal 2024; 11(4): e01312 doi: 10.14309/crj.0000000000001312
11
Martin Prescher, Tim Kroll, Lutz Schmitt. ABCB4/MDR3 in health and disease – at the crossroads of biochemistry and medicineBiological Chemistry 2019; 400(10): 1245 doi: 10.1515/hsz-2018-0441
12
Eva Sticova, Milan Jirsa. ABCB4 disease: Many faces of one gene deficiencyAnnals of Hepatology 2020; 19(2): 126 doi: 10.1016/j.aohep.2019.09.010
13
Lavinija Matakovic, Arend W. Overeem, Karin Klappe, Sven C. D. van IJzendoorn. HepatocytesMethods in Molecular Biology 2022; 2544: 71 doi: 10.1007/978-1-0716-2557-6_4
14
Jorge Mallea, Candice Bolan, Cherise Cortese, Denise Harnois. Cystic Fibrosis–Associated Liver Disease in Lung Transplant RecipientsLiver Transplantation 2019; 25(8): 1265 doi: 10.1002/lt.25496
15
Tim Kroll, Sander H.J. Smits, Lutz Schmitt. Monomeric bile acids modulate the ATPase activity of detergent-solubilized ABCB4/MDR3Journal of Lipid Research 2021; 62: 100087 doi: 10.1016/j.jlr.2021.100087
16
Min Ji Sohn, Min Hyung Woo, Moon-Woo Seong, Sung Sup Park, Gyeong Hoon Kang, Jin Soo Moon, Jae Sung Ko. Benign Recurrent Intrahepatic Cholestasis Type 2 in Siblings with Novel ABCB11 MutationsPediatric Gastroenterology, Hepatology & Nutrition 2019; 22(2): 201 doi: 10.5223/pghn.2019.22.2.201
17
Patryk Lipiński, Elżbieta Ciara, Dorota Jurkiewicz, Rafał Płoski, Marta Wawrzynowicz-Syczewska, Joanna Pawłowska, Irena Jankowska. Progressive familial intrahepatic cholestasis type 3: Report of four clinical cases, novel ABCB4 variants and long-term follow-upAnnals of Hepatology 2021; 25: 100342 doi: 10.1016/j.aohep.2021.100342
18
Eleni V. Geladari, Natalia G. Vallianou, Evangelia Margellou, Dimitris Kounatidis, Vassilios Sevastianos, Alexandra Alexopoulou. Benign Recurrent Intrahepatic Cholestasis: Where Are We Now?Gastroenterology Insights 2024; 15(1): 156 doi: 10.3390/gastroent15010011
19
Melissa Palmer, Arie Regev, Keith Lindor, Mark I. Avigan, Lara Dimick‐Santos, William Treem, John F. Marcinak, James H. Lewis, Frank A. Anania, Daniel Seekins, Benjamin L. Shneider, Naga Chalasani. Consensus guidelines: best practices for detection, assessment and management of suspected acute drug‐induced liver injury occurring during clinical trials in adults with chronic cholestatic liver diseaseAlimentary Pharmacology & Therapeutics 2020; 51(1): 90 doi: 10.1111/apt.15579
20
Eva Sticova, Magdalena Neroldova, Radana Kotalova, Iva Subhanova, Milan Jirsa. ABCB4 disease mimicking morbus Wilson: A potential diagnostic pitfallBiomedical Papers 2020; 164(1): 121 doi: 10.5507/bp.2019.054
21
Ming Li, Qian Wang, Yong Li, Shengtian Cao, Yingjun Zhang, Zhongqing Wang, Guozhu Liu, Jing Li, Baohua Gu. Apical sodium-dependent bile acid transporter, drug target for bile acid related diseases and delivery target for prodrugs: Current and future challengesPharmacology & Therapeutics 2020; 212: 107539 doi: 10.1016/j.pharmthera.2020.107539
22
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 literaturesOrphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-022-02597-y
23
Tim Kroll, Martin Prescher, Sander H. J. Smits, Lutz Schmitt. Structure and Function of Hepatobiliary ATP Binding Cassette TransportersChemical Reviews 2021; 121(9): 5240 doi: 10.1021/acs.chemrev.0c00659
24
Christoph Jüngst, Christina Justinger, Janett Fischer, Thomas Berg, Frank Lammert. Common <b><i>ABCB4</i></b> and <b><i>ABCB11</i></b> Genotypes Are Associated with Idiopathic Chronic Cholestasis in AdultsDigestive Diseases 2022; 40(4): 489 doi: 10.1159/000518203
25
Holmfridur Helgadottir, Geir Folvik, Mette Vesterhus. Improvement of cholestatic episodes in patients with benign recurrent intrahepatic cholestasis (BRIC) treated with rifampicin. A long-term follow-upScandinavian Journal of Gastroenterology 2023; 58(5): 512 doi: 10.1080/00365521.2022.2143725
26
Eric Arthur Lorio, David Valadez, Naim Alkhouri, Nicole Loo. Cholestasis in Benign Recurrent Intrahepatic Cholestasis 2ACG Case Reports Journal 2020; 7(6): e00412 doi: 10.14309/crj.0000000000000412
27
Kazuto Tajiri, Yukihiro Shimizu. Recent advances in the management of pruritus in chronic liver diseasesWorld Journal of Gastroenterology 2017; 23(19): 3418-3426 doi: 10.3748/wjg.v23.i19.3418
28
Eva-Doreen Pfister, Veronika K Jaeger, André Karch, Denys Shay, Nagoud Schukfeh, Johanna Ohlendorf, Norman Junge, Imeke Goldschmidt, Amelie Stalke, Verena Keitel-Anselmino, Ulrich Baumann. Native liver survival in bile salt export pump deficiency: results of a retrospective cohort studyHepatology Communications 2023; 7(4) doi: 10.1097/HC9.0000000000000092
29
Peter Hegyi, Jozsef Maléth, Julian R. Walters, Alan F. Hofmann, Stephen J. Keely. Guts and Gall: Bile Acids in Regulation of Intestinal Epithelial Function in Health and DiseasePhysiological Reviews 2018; 98(4): 1983 doi: 10.1152/physrev.00054.2017
30
Sara Hassan, Paula Hertel. Overview of Progressive Familial Intrahepatic CholestasisClinics in Liver Disease 2022; 26(3): 371 doi: 10.1016/j.cld.2022.03.003
31
Yue Wang, Yin-Ling Wang, Yue-Ping Zhu, Wei-Lu Xu, Jin-Long Huang, Xiao-Zhe Chai, Ming Li, Feng Qian, Chuan-Wu Zhu. Type 3 progressive familial intrahepatic cholestasis combined with autoimmune hepatitis-primary biliary cirrhosis overlap syndrome: A case reportWorld Chinese Journal of Digestology 2022; 30(1): 56 doi: 10.11569/wcjd.v30.i1.56
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32
Ben-Ping Zhang, Zhi-Hua Huang, Chen Dong. Biliary atresia combined with progressive familial intrahepatic cholestasis type 3Medicine 2019; 98(19): e15593 doi: 10.1097/MD.0000000000015593
33
Tengqi Ren, Liwei Pang, Wanlin Dai, Shuodong Wu, Jing Kong. Regulatory mechanisms of the bile salt export pump (BSEP/ABCB11) and its role in related diseasesClinics and Research in Hepatology and Gastroenterology 2021; 45(6): 101641 doi: 10.1016/j.clinre.2021.101641
34
Kazunori Yoh, Hiroki Nishikawa, Hirayuki Enomoto, Yoshinori Iwata, Akio Ishii, Yukihisa Yuri, Noriko Ishii, Yuho Miyamoto, Kunihiro Hasegawa, Chikage Nakano, Ryo Takata, Takashi Nishimura, Nobuhiro Aizawa, Yoshiyuki Sakai, Naoto Ikeda, Tomoyuki Takashima, Hiroko Iijima, Shuhei Nishiguchi. Effect of nalfurafine hydrochloride in patients with chronic liver disease with refractory pruritus on sleep disorders: a study protocol for single-arm, prospective, interventional studyBMJ Open Gastroenterology 2017; 4(1): e000177 doi: 10.1136/bmjgast-2017-000177
35
Beatriz Mínguez Rodríguez, Cristina Molera Busoms, Loreto Martorell Sampol, Ruth García Romero, Gemma Colomé Rivero, Javier Martín de Carpi. Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohortGastroenterología y Hepatología (English Edition) 2022; 45(8): 585 doi: 10.1016/j.gastre.2021.12.004
36
Adil Salyani, Linda Barasa, Allan Rajula, Sayed K. Ali. Benign Recurrent Intrahepatic Cholestasis (BRIC): An African Case ReportCase Reports in Gastrointestinal Medicine 2020; 2020: 1 doi: 10.1155/2020/2894293
37
Antonia Felzen, Henkjan J. Verkade. The spectrum of Progressive Familial Intrahepatic Cholestasis diseases: Update on pathophysiology and emerging treatmentsEuropean Journal of Medical Genetics 2021; 64(11): 104317 doi: 10.1016/j.ejmg.2021.104317
38
Verena Keitel-Anselmino. Therapie-Handbuch - Gastroenterologie und Hepatologie2021; : 356 doi: 10.1016/B978-3-437-23847-5.00050-8
39
Jawaher Abdullah Alamoudi, Wenkuan Li, Nagsen Gautam, Marco Olivera, Jane Meza, Sandeep Mukherjee, Yazen Alnouti. Bile acid indices as biomarkers for liver diseases I: Diagnostic markersWorld Journal of Hepatology 2021; 13(4): 433-455 doi: 10.4254/wjh.v13.i4.433
40
Shuying Xie, Shizhang Wei, Xiao Ma, Ruilin Wang, Tingting He, Zhao Zhang, Ju Yang, Jiawei Wang, Lei Chang, Manyi Jing, Haotian Li, Xuelin Zhou, Yanling Zhao. Genetic alterations and molecular mechanisms underlying hereditary intrahepatic cholestasisFrontiers in Pharmacology 2023; 14 doi: 10.3389/fphar.2023.1173542
41
Samiksha Gupta, Ijlal Akbar Ali, Eleanor Abreo, Veena Gujju, Maham Hayat. The Mystery of Episodic Recurrent Jaundice in a Young Male: Cholestasis With a Normal Gamma-Glutamyl TransferaseCureus 2021;  doi: 10.7759/cureus.13834
42
Jonathan M. Moore, Eric L. Bell, Robert O. Hughes, Alastair S. Garfield. ABC transporters: human disease and pharmacotherapeutic potentialTrends in Molecular Medicine 2023; 29(2): 152 doi: 10.1016/j.molmed.2022.11.001
43
Davor Slijepcevic, Reinout L.P. Roscam Abbing, Claudia D. Fuchs, Lizette C.M. Haazen, Ulrich Beuers, Michael Trauner, Ronald P.J. Oude Elferink, Stan F.J. van de Graaf. Na+‐taurocholate cotransporting polypeptide inhibition has hepatoprotective effects in cholestasis in miceHepatology 2018; 68(3): 1057 doi: 10.1002/hep.29888
44
James Neuberger. Liver Transplantation2021; : 445 doi: 10.1002/9781119634010.ch49
45
Amil Sinha, Meha Bhuva, Claire Grant, Alexander E. Gimson, Edward Thompson, Adam Duckworth, Susan E. Davies, Guruprasad Aithal, William J. Griffiths. ABCB4 Mutations in Adults Cause a Spectrum Cholestatic Disorder Histologically Distinct from Other Biliary DiseaseDigestive Diseases and Sciences 2022; 67(12): 5551 doi: 10.1007/s10620-022-07416-9
46
Willemien F.J. Hof, Jan Freark de Boer, Henkjan J. Verkade. Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trialsExpert Opinion on Emerging Drugs 2024;  doi: 10.1080/14728214.2024.2336986
47
Binita M. Kamath, Philip Stein, Roderick H. J. Houwen, Henkjan J. Verkade. Potential of ileal bile acid transporter inhibition as a therapeutic target in Alagille syndrome and progressive familial intrahepatic cholestasisLiver International 2020; 40(8): 1812 doi: 10.1111/liv.14553
48
Haibing Gao, Shenglong Lin, Xujiang Lv, Huaxi Ma, Xiangmei Wang, Jiankai Fang, Wenjun Wu, Jiahuang Lin, Xiumin Chen, Minghua Lin. The Identification of Two New ABCB11 Gene Mutations and the Treatment Outcome in a Young Adult with Benign Recurrent Intrahepatic Cholestasis: A Case ReportHepatitis Monthly 2017; 17(10) doi: 10.5812/hepatmon.55087
49
Roderick Houwen. Chapter 6.4. Diagnostic Progress in CholestasisJournal of Pediatric Gastroenterology and Nutrition 2018; 66(S1) doi: 10.1097/MPG.0000000000001916
50
Aradhana Aneja, Elizabeth Scott, Rohit Kohli. Advances in management of end stage liver disease in childrenMedical Journal Armed Forces India 2021; 77(2): 129 doi: 10.1016/j.mjafi.2021.03.001
51
Patryk Lipiński, Joanna Pawłowska, Irena Jankowska. Łagodna nawracająca cholestaza wewnątrzwątrobowaPediatria Polska 2017; 92(5): 575 doi: 10.1016/j.pepo.2017.03.010
52
Wafaa Ahmed, Rebecca Jeyaraj, David Reffitt, John Devlin, Abid Suddle, John Hunt, Michael A Heneghan, Phillip Harrison, Deepak Joshi. Nasobiliary drainage: an effective treatment for pruritus in cholestatic liver diseaseFrontline Gastroenterology 2022; 13(5): 416 doi: 10.1136/flgastro-2021-102025
53
Huayu Chen, Dongbo Wu, Wei Jiang, Ting Lei, Changli Lu, Taoyou Zhou. Case Report: A Novel Homozygous Variant Identified in a Chinese Patient With Benign Recurrent Intrahepatic Cholestasis-Type 1Frontiers in Medicine 2021; 8 doi: 10.3389/fmed.2021.705489
54
Hamid Reza Foroutan, Ali Bahador, Sultan Mohsin Ghanim, Seyed Mohsen Dehghani, Mohammad Hossein Anbardar, Mohammad Reza Fattahi, Mehdi Forooghi, Omidreza Azh, Ali Tadayon, Alireza Sherafat, Amir Arsalan Yaghoobi, Mohammad Ali Ashraf. Effects of partial internal biliary diversion on long-term outcomes in patients with progressive familial intrahepatic cholestasis: experience in 44 patientsPediatric Surgery International 2020; 36(5): 603 doi: 10.1007/s00383-020-04641-z
55
Philipp Schreiner, Bruno Stieger, Valérie McLin, Anne‐Laure Rougemont, Verena Keitel, Carola Dröge, Beat Müllhaupt. A rare cause of a cholestatic jaundice in a North African teenagerLiver International 2019; 39(11): 2036 doi: 10.1111/liv.14122
56
Henkjan J. Verkade, Richard J. Thompson, Henrik Arnell, Björn Fischler, Per‐Göran Gillberg, Jan P. Mattsson, Kristina Torfgård, Erik Lindström. Systematic Review and Meta‐analysisJournal of Pediatric Gastroenterology and Nutrition 2020; 71(2): 176 doi: 10.1097/MPG.0000000000002789