Academic Content and Language Evaluation of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (5674)
All Articles published online
|
Publishing Process of This Article
|
May 21, 2014 (publication date) through May 8, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: |
Jirsa M, Bronský J, Dvořáková L, Šperl J, Šmajstrla V, Horák J, Nevoral J, Hřebíček M. |
|---|---|
| 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 Cases. Cureus 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 Review. International 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 pregnancy. Scientific 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 Cholestasis. Journal 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 Kingdom. Scientific 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 underdiagnosed. Digestive 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 pregnancy. Clinics 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 patients. Arab 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 Cholelithiasis. Genes 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 review. The 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 teenager. Liver 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 Cholecystolithiasis. Frontiers 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 Infant. JPGN 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 3. Biomarkers 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 review. Journal 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 Gallstones. Journal of Pediatric Gastroenterology and Nutrition 2019; 69(2): 138 doi: 10.1097/MPG.0000000000002353
|