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Jun 7, 2007 (publication date) through Apr 18, 2024
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Publication Name
World Journal of Gastroenterology
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1007-9327
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Dhillon BK, Das R, Garewal G, Chawla Y, Dhiman R, Das A, Duseja A, Chandak G. Frequency of primary iron overload and HFE gene mutations (C282Y, H63D and S65C) in chronic liver disease patients in north India. World J Gastroenterol 2007; 13(21): 2956-2959 [PMID: 17589946 DOI: 10.3748/wjg.v13.i21.2956] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v13/i21/2956.htm |
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BARJINDERJIT KAUR DHILLON, SWAMI PRAKASH, G. R. CHANDAK, Y. K. CHAWLA, REENA DAS. H63D mutation in HFE gene is common in Indians and is associated with the European haplotype. Journal of Genetics 2012; 91(2): 229 doi: 10.1007/s12041-012-0163-5
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I. V. Paltsev, A. L. Kalinin. MUTATIONS OF GENE HFE AS A RISK FACTOR OF HEMOCHROMATOSIS DEVELOPMENT AT PATIENT WITH CHRONIC DIFFUSE LIVER DISEASES. Health and Ecology Issues 2010; (4): 53 doi: 10.51523/2708-6011.2010-7-4-10
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Zahra Jowkar, Bita Geramizadeh, Mahmoud Shariat. Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis. Hepatitis Monthly 2011; 11(11): 887 doi: 10.5812/kowsar.1735143X.3749
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Qing Ye, Bao-Xin Qian, Wei-Li Yin, Feng-Mei Wang, Tao Han, Pavel Strnad. Association between the HFE C282Y, H63D Polymorphisms and the Risks of Non-Alcoholic Fatty Liver Disease, Liver Cirrhosis and Hepatocellular Carcinoma: An Updated Systematic Review and Meta-Analysis of 5,758 Cases and 14,741 Controls. PLOS ONE 2016; 11(9): e0163423 doi: 10.1371/journal.pone.0163423
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Reena Das, Jasmina Ahluwalia, Man Updesh Singh Sachdeva. Hematological Practice in India. Hematology/Oncology Clinics of North America 2016; 30(2): 433 doi: 10.1016/j.hoc.2015.11.009
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Ling Nie, Lin Li, Lin Yang, Yue Zhang, Zhijian Xiao. HFE genotype and iron metabolism in Chinese patients with myelodysplastic syndromes and aplastic anemia. Annals of Hematology 2010; 89(12): 1249 doi: 10.1007/s00277-010-1016-z
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Darrell H. G. Crawford, Linda M. Fletcher, Kris V. Kowdley. Iron Physiology and Pathophysiology in Humans. 2012; : 441 doi: 10.1007/978-1-60327-485-2_22
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Bhuvana Selvaraj, Sangeetha Soundararajan, Shettu Narayanasamy, Ganesan Subramanian, Senthil Kumar Ramanathan. Frequency of hereditary hemochromatosis gene mutations and their effects on iron overload among beta thalassemia patients of Chennai residents. AIMS Molecular Science 2021; 8(4): 233 doi: 10.3934/molsci.2021018
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Abraham Koshy, Roy J. Mukkada, Antony P. Chettupuzha, Jose V. Francis, Julio C. Kandathil, Pushpa Mahadevan. Hemochromatosis in India: First Report of Whole Exome Sequencing With Review of the Literature. Journal of Clinical and Experimental Hepatology 2020; 10(2): 163 doi: 10.1016/j.jceh.2019.04.051
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Nihal Salah Ibrahim, Mohamed Menesy. Hemochromatosis gene mutations in chronic hepatitis “C” patients. Comparative Clinical Pathology 2016; 25(2): 375 doi: 10.1007/s00580-015-2193-x
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Yoji Ishizu, Yoshiaki Katano, Takashi Honda, Kazuhiko Hayashi, Masatoshi Ishigami, Akihiro Itoh, Yoshiki Hirooka, Isao Nakano, Hidemi Goto. Clinical impact of HFE mutations in Japanese patients with chronic hepatitis C. Journal of Gastroenterology and Hepatology 2012; 27(6): 1112 doi: 10.1111/j.1440-1746.2011.06976.x
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Saumya Madushani Samarasinghe, Asanka Sudeshini Hewage, Rohan Chaminda Siriwardana, Kamani Hemamala Tennekoon, Madunil Anuk Niriella, Sumadee De Silva. Genetic and metabolic aspects of non-alcoholic fatty liver disease (NAFLD) pathogenicity. Egyptian Journal of Medical Human Genetics 2023; 24(1) doi: 10.1186/s43042-023-00433-x
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James E. Nelson, Heather Klintworth, Kris V. Kowdley. Iron Metabolism in Nonalcoholic Fatty Liver Disease. Current Gastroenterology Reports 2012; 14(1): 8 doi: 10.1007/s11894-011-0234-4
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Yan-yan Xu, Yu-han Tang, Xiao-ping Guo, Jing Wang, Ping Yao. HFE genetic variability and risk of alcoholic liver disease: A meta-analysis. Journal of Huazhong University of Science and Technology [Medical Sciences] 2016; 36(5): 626 doi: 10.1007/s11596-016-1637-0
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Reena Das, Giriraj Ratan Chandak. Obscure pathogenesis of primary iron overload in Indians warrants more focused research. Indian Journal of Gastroenterology 2011; 30(4): 154 doi: 10.1007/s12664-011-0119-3
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Agustin Castiella. Iron Overload and HFE Mutations: Are They Relevant in Cryptogenic Cirrhosis?. Hepatitis Monthly 2012; 12(2): 126 doi: 10.5812/hepatmon.4875
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Rekha Athiyarath, Alok Srivastava, Eunice Sindhuvi Edison. Molecular basis of primary iron overload in India and the role of serum-derived factors in hepcidin regulation. Annals of Hematology 2013; 92(6): 843 doi: 10.1007/s00277-012-1621-0
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Prachi S. Patil, K. M. Mohandas. Primary iron overload and HFE gene mutations in North Indian adults. Indian Journal of Gastroenterology 2012; 31(1): 36 doi: 10.1007/s12664-012-0170-8
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Mithun Sharma, Shasikala Mitnala, Ravi K. Vishnubhotla, Rathin Mukherjee, Duvvur N. Reddy, Padaki N. Rao. The Riddle of Nonalcoholic Fatty Liver Disease: Progression From Nonalcoholic Fatty Liver to Nonalcoholic Steatohepatitis. Journal of Clinical and Experimental Hepatology 2015; 5(2): 147 doi: 10.1016/j.jceh.2015.02.002
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Pierre Brissot, Marie-Bérengère Troadec, Edouard Bardou-Jacquet, Caroline Le Lan, Anne-Marie Jouanolle, Yves Deugnier, Olivier Loréal. Current approach to hemochromatosis. Blood Reviews 2008; 22(4): 195 doi: 10.1016/j.blre.2008.03.001
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Etheresia Pretorius, Janette Bester, Natasha Vermeulen, Boguslaw Lipinski, George S. Gericke, Douglas B. Kell, Thiruma V. Arumugam. Profound Morphological Changes in the Erythrocytes and Fibrin Networks of Patients with Hemochromatosis or with Hyperferritinemia, and Their Normalization by Iron Chelators and Other Agents. PLoS ONE 2014; 9(1): e85271 doi: 10.1371/journal.pone.0085271
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Danny Con, Amanda J. Nicoll. Hyperferritinaemia and iron overload in Asian patients: lessons from an Australian tertiary centre experience. Internal Medicine Journal 2021; 51(5): 802 doi: 10.1111/imj.15316
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Mohd Talha Noor, Manish Tiwari, Ravindra Kumar. Non-HFE iron overload as a surrogate marker of disease severity in patients of liver cirrhosis. Indian Journal of Gastroenterology 2016; 35(1): 33 doi: 10.1007/s12664-016-0623-6
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Shalu Jain, Sarita Agarwal, Parag Tamhankar, Prashant Verma, Gourdas Choudhuri. Lack of association of primary iron overload and common HFE gene mutations with liver cirrhosis in adult Indian population. Indian Journal of Gastroenterology 2011; 30(4): 161 doi: 10.1007/s12664-011-0109-5
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V. M. Mitsura, T. L. Krasavtsev, E. V. Voropaev, O. Yu. Baranov, I. V. Paltsev, A. L. Kalinin. THE FREQUENCY OF HFE GENE MUTATIONS C282Y AND H63D REVEALING IN PATIENTS WITH CHRONIC HEPATITIS AND LIVER CIRRHOSIS OF DIFFERENT ETIOLOGY. Health and Ecology Issues 2008; (2): 56 doi: 10.51523/2708-6011.2008-5-2-12
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