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Cited by in CrossRef
For: Jirsa M, Bronský J, Dvořáková L, Šperl J, Šmajstrla V, Horák J, Nevoral J, Hřebíček M. ABCB4 mutations underlie hormonal cholestasis but not pediatric idiopathic gallstones. World J Gastroenterol 2014; 20(19): 5867-5874 [PMID: 24914347 DOI: 10.3748/wjg.v20.i19.5867]
URL: https://www.wjgnet.com/1007-9327/full/v20/i19/5867.htm
Number Citing Articles
1
P. Goubault, T. Brunel, A. Rode, B. Bancel, K. Mohkam, J.-Y. Mabrut. Syndrome Low-Phospholipid Associated Cholelithiasis (LPAC)Journal de Chirurgie Viscérale 2019; 156(4): 344 doi: 10.1016/j.jchirv.2019.01.005
2
Fatima Zahra Belabbes, Amine Benfaida, Bouknani Nawal, Abdennaceur El Idrissi Lamghari, Fedoua Rouibaa. Low Phospholipid-Associated Cholelithiasis: Contribution of Imaging in Two CasesCureus 2022;  doi: 10.7759/cureus.22383
3
Katarzyna Zdanowicz, Jaroslaw Daniluk, Dariusz Marek Lebensztejn, Urszula Daniluk. The Etiology of Cholelithiasis in Children and Adolescents—A Literature ReviewInternational Journal of Molecular Sciences 2022; 23(21): 13376 doi: 10.3390/ijms232113376
4
Peter H. Dixon, Melissa Sambrotta, Jennifer Chambers, Pamela Taylor-Harris, Argyro Syngelaki, Kypros Nicolaides, A. S. Knisely, Richard J. Thompson, Catherine Williamson. An expanded role for heterozygous mutations of ABCB4, ABCB11, ATP8B1, ABCC2 and TJP2 in intrahepatic cholestasis of pregnancyScientific Reports 2017; 7(1) doi: 10.1038/s41598-017-11626-x
5
Paula M. Hertel, Laura N. Bull, Richard J. Thompson, Nathan P. Goodrich, Wen Ye, John C. Magee, Robert H. Squires, Lee M. Bass, James E. Heubi, Grace E. Kim, Sarangarajan Ranganathan, Kathleen B. Schwarz, Molly A. Bozic, Simon P. Horslen, Matthew S. Clifton, Yumirle P. Turmelle, Frederick J. Suchy, Riccardo A. Superina, Kasper S. Wang, Kathleen M. Loomes, Binita M. Kamath, Ronald J. Sokol, Benjamin L. Shneider. Mutation Analysis and Disease Features at Presentation in a Multi‐Center Cohort of Children With Monogenic CholestasisJournal of Pediatric Gastroenterology and Nutrition 2021; 73(2): 169 doi: 10.1097/MPG.0000000000003153
6
Julia Zöllner, Sarah Finer, Kenneth J. Linton, Shaheen Akhtar, Mohammad Anwar, Elena Arciero, Samina Ashraf, Saeed Bidi, Gerome Breen, James Broster, Raymond Chung, David Collier, Charles J. Curtis, Shabana Chaudhary, Megan Clinch, Grainne Colligan, Panos Deloukas, Ceri Durham, Faiza Durrani, Fabiola Eto, Sarah Finer, Joseph Gafton, Ana Angel Garcia, Chris Griffiths, Joanne Harvey, Teng Heng, Sam Hodgson, Qin Qin Huang, Matt Hurles, Karen A. Hunt, Shapna Hussain, Kamrul Islam, Vivek Iyer, Ben Jacobs, Ahsan Khan, Cath Lavery, Sang Hyuck Lee, Robin Lerner, Daniel MacArthur, Daniel Malawsky, Hilary Martin, Dan Mason, Rohini Mathur, Mohammed Bodrul Mazid, John McDermott, Caroline Morton, Bill Newman, Elizabeth Owor, Asma Qureshi, Samiha Rahman, Shwetha Ramachandrappa, Mehru Reza, Jessry Russell, Nishat Safa, Miriam Samuel, Michael Simpson, John Solly, Marie Spreckley, Daniel Stow, Michael Taylor, Richard C. Trembath, Karen Tricker, Nasir Uddin, David A. van Heel, Klaudia Walter, Caroline Winckley, Suzanne Wood, John Wright, Julia Zöllner, David A. van Heel, Catherine Williamson, Peter H. Dixon. Rare variant contribution to cholestatic liver disease in a South Asian population in the United KingdomScientific Reports 2023; 13(1) doi: 10.1038/s41598-023-33391-w
7
Antonella Avena, Sandro Puggelli, Michael Morris, Andreas Cerny, Alfredo Repáraz Andrade, Emmanuela Pareti, Florian Bihl, Daniele Cassatella, Isabelle Moix, Elisabetta Merlo, Anne-Laure Rougemont, Pietro Majno-Hurst, Diego Vergani, Giorgina Mieli-Vergani, Benedetta Terziroli Beretta-Piccoli. ABCB4 variants in adult patients with cholestatic disease are frequent and underdiagnosedDigestive and Liver Disease 2021; 53(3): 329 doi: 10.1016/j.dld.2020.12.003
8
Peter H. Dixon, Catherine Williamson. The pathophysiology of intrahepatic cholestasis of pregnancyClinics and Research in Hepatology and Gastroenterology 2016; 40(2): 141 doi: 10.1016/j.clinre.2015.12.008
9
Yosra Halleb, Elhem Ben Jazia, Imen Akkari, Houneida Zaghouani, Fahmi Hmila, Rafik Ghrissi, Ali Saad, Moez Gribaa. Clinical, biological, radiological, and genetic study of LPAC syndrome in Tunisian patientsArab Journal of Gastroenterology 2022; 23(3): 210 doi: 10.1016/j.ajg.2022.06.002
10
Helen H. Wang, Piero Portincasa, Min Liu, David Q.-H. Wang. Genetic Analysis of ABCB4 Mutations and Variants Related to the Pathogenesis and Pathophysiology of Low Phospholipid-Associated CholelithiasisGenes 2022; 13(6): 1047 doi: 10.3390/genes13061047
11
Weronika Niemyjska-Dmoch, Przemysław Kosiński, Piotr Węgrzyn, Katarzyna Luterek, Aleksandra Jezela-Stanek. Intrahepatic cholestasis of pregnancy and theory of inheritance of the disease. Literature reviewThe Journal of Maternal-Fetal & Neonatal Medicine 2023; 36(2) doi: 10.1080/14767058.2023.2279020
12
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
13
Lingling Hou, Cuifang Hu, Lili Ji, Qiongdan Wang, Min Liang. The Mitochondrial tRNAPhe 625G>A Mutation in Three Han Chinese Families With CholecystolithiasisFrontiers in Genetics 2022; 13 doi: 10.3389/fgene.2022.814729
14
Radhapyari Lourembam,, Rohan Malik,, Rishi Bolia. Combined Mutations of Canalicular Transporter Proteins Causing Low Phospholipid-Associated Cholelithiasis and Transient Neonatal Cholestasis in an InfantJPGN Reports 2021; 2(2): e080 doi: 10.1097/PG9.0000000000000080
15
Catarina Gouveia, Margarida Flor de Lima, Flávio Pereira, Bruno Rosa, José Cotter, António Banhudo, Maria Duarte, Alexandre Ferreira, Marília Cravo, Joana Nunes. Should patients with symptomatic cholelithiasis before 30 years of age be tested for ABCB4 gene mutations?Scandinavian Journal of Gastroenterology 2020; 55(8): 958 doi: 10.1080/00365521.2020.1790648
16
Mona Fathy, Manal Kamal, Marwa Al-Sharkawy, Hanaa Al-Karaksy, Nora Hassan. Molecular characterization of exons 6, 8 and 9 of ABCB4 gene in children with Progressive Familial Intrahepatic Cholestasis type 3Biomarkers 2016; 21(7): 573 doi: 10.3109/1354750X.2016.1166264
17
P. Goubault, T. Brunel, A. Rode, B. Bancel, K. Mohkam, J.-Y. Mabrut. Low-Phospholipid Associated Cholelithiasis (LPAC) syndrome: A synthetic reviewJournal of Visceral Surgery 2019; 156(4): 319 doi: 10.1016/j.jviscsurg.2019.02.006
18
Antti Koivusalo, Annika Mutanen, Markku Nissinen, Helena Gylling, Mikko Pakarinen. Altered Bile Transporter Expression and Cholesterol Metabolism in Children With Cholesterol and Pigment GallstonesJournal of Pediatric Gastroenterology and Nutrition 2019; 69(2): 138 doi: 10.1097/MPG.0000000000002353
19
Julia Zöllner, Catherine Williamson, Peter H Dixon. Genetic issues in ICPObstetric Medicine 2024; 17(3): 157 doi: 10.1177/1753495X241263441