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Diagnosis and treatment of hereditary hemochromatosis: an update

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Pages 517-530 | Published online: 10 Jan 2014

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Pierre Brissot. (2016) Optimizing the diagnosis and the treatment of iron overload diseases. Expert Review of Gastroenterology & Hepatology 10:3, pages 359-370.
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Zahrah T. Althagafi, Hassan A. Arida & Reham F. Hassan. (2022) Novel Application for Activated Carbon Pharmaceutical Formulation as an Efficient Adsorbent of Iron (III) from Contaminated Canned Food. Journal of Chemistry 2022, pages 1-7.
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Donald Turbiville, Xiaotang Du, Jacob Yo, Bagi R Jana & Jianli Dong. (2019) Iron Overload in an HFE Heterozygous Carrier: A Case Report and Literature Review . Laboratory Medicine 50:2, pages 212-217.
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Eva Rombout-Sestrienkova, Marian G. J. van Kraaij & Ger H. Koek. (2016) How we manage patients with hereditary haemochromatosis. British Journal of Haematology 175:5, pages 759-770.
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Sim Y. Ong, Amanda J. Nicoll & Martin B. Delatycki. (2016) How should hyperferritinaemia be investigated and managed?. European Journal of Internal Medicine 33, pages 21-27.
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Yang‐Fan Lv, Xian Chang, Rui‐Xi Hua, Guang‐Ning Yan, Gang Meng, Xiao‐Yu Liao, Xi Zhang & Qiao‐Nan Guo. (2016) The risk of new‐onset cancer associated with HFE C282Y and H63D mutations: evidence from 87,028 participants . Journal of Cellular and Molecular Medicine 20:7, pages 1219-1233.
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Menaka Sivakumar & Lawrie W Powell. (2016) Management of human factors engineering-associated hemochromatosis: A 2015 update. World Journal of Hepatology 8:8, pages 395.
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Priya Handa & Kris V. Kowdley. (2016) A Proton Pump Inhibitor a Day Keeps the Iron Away. Clinical Gastroenterology and Hepatology 14:1, pages 153-155.
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Ruo-kun Li, Suzanne L. Palmer, Meng-su Zeng, Jin-wei Qiang, Frank Chen, Sheng-xiang Rao, Ling-li Chen & Yong-ming Dai. (2015) Detection of Endogenous Iron Reduction during Hepatocarcinogenesis at Susceptibility-Weighted MR Imaging: Value for Characterization of Hepatocellular Carcinoma and Dysplastic Nodule in Cirrhotic Liver. PLOS ONE 10:11, pages e0142882.
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Priya Handa & Kris V. Kowdley. (2015) Glyceronephosphate O‐acyltransferase as a hemochromatosis modifier gene: Another iron in the fire?. Hepatology 62:2, pages 337-339.
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S.-R. Chen, L.-Q. Yang, Y.-T. Chong, Y.-S. Jie, Y.-K. Wu, J. Yang, G.-L. Lin & X.-H. Li. (2015) Novel gain of function mutation in the SLC40A1 gene associated with hereditary haemochromatosis type 4 . Internal Medicine Journal 45:6, pages 672-676.
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Ieva Mažeikaitė, Dalius Banionis, Sigitas Laima & Algimantas Jasulaitis. (2015) Hemochromatozės diagnostika ir autopsijos reikšmė. Klinikinis atvejis. Sveikatos mokslai 26:2, pages 53-58.
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Dilum Ekanayake, Clinton Roddick & Lawrie W. Powell. (2015) Recent advances in hemochromatosis: a 2015 update. Hepatology International 9:2, pages 174-182.
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Heinz Zoller & Armin Finkenstedt. (2015) Should C282Y homozygotes with mild iron overload be treated?. Journal of Hepatology 62:3, pages 510-511.
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Reena J. Salgia & Kimberly Brown. (2015) Diagnosis and Management of Hereditary Hemochromatosis. Clinics in Liver Disease 19:1, pages 187-198.
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Dilum Ekanayake, Clinton Roddick, Murtaza Khanbhai & Lawrie W. Powell. (2015) Homozygosity For The C282Y Substitution In The HFE Gene: The Incomplete Penetrance And Variable Expressivity. EMJ Hepatology, pages 79-85.
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John C. Wood. (2014) Use of Magnetic Resonance Imaging to Monitor Iron Overload. Hematology/Oncology Clinics of North America 28:4, pages 747-764.
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Yatrik M. Shah & Liwei Xie. (2014) Hypoxia-Inducible Factors Link Iron Homeostasis and Erythropoiesis. Gastroenterology 146:3, pages 630-642.
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Etheresia Pretorius & Douglas B. Kell. (2014) Diagnostic morphology: biophysical indicators for iron-driven inflammatory diseases. Integr. Biol. 6:5, pages 486-510.
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Pushpjeet Kanwar & Kris V. Kowdley. (2014) Metal Storage Disorders. Medical Clinics of North America 98:1, pages 87-102.
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