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Liver and biliary tract

Health check-ups and family screening allow detection of hereditary hemochromatosis with less advanced liver fibrosis and survival comparable with the general population

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Pages 1118-1126 | Received 06 Mar 2011, Accepted 18 May 2011, Published online: 15 Jun 2011

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. (2011) This month in Scandinavian Journal of Gastroenterology. Scandinavian Journal of Gastroenterology 46:9, pages 1027-1028.
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James C. Barton, J. Clayborn Barton, Neha Patel & Gordon D. McLaren. (2021) Abdominal pain and cirrhosis at diagnosis of hemochromatosis: Analysis of 219 referred probands with HFE p.C282Y homozygosity and a literature review. PLOS ONE 16:12, pages e0261690.
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Carl Eckerström, Sofia Frändberg, Lena Lyxe, Cecilia Pardi & Jan Konar. (2020) Evaluation of a screening program for iron overload andHFE mutations in 50,493 blood donors. Annals of Hematology 99:10, pages 2295-2301.
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Hanzhang Xu, Paulin Straughan, Wei Pan, Zhihong Zhen & Bei Wu. (2016) Validating a Scale of Health Beliefs in Preventive Health Screenings Among Chinese Older Adults . Journal of Transcultural Nursing 28:5, pages 464-472.
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Graça Porto, Pierre Brissot, Dorine W Swinkels, Heinz Zoller, Outi Kamarainen, Simon Patton, Isabel Alonso, Michael Morris & Steve Keeney. (2015) EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). European Journal of Human Genetics 24:4, pages 479-495.
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Catherine Ogilvie, Dairena Gaffney, Heather Murray, Andrew Kerry, Caroline Haig, Richard Spooner & Edward J Fitzsimons. (2015) Improved detection of hereditary haemochromatosis. Journal of Clinical Pathology 68:3, pages 218-221.
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Christina Ellervik, Jacob Louis Marott, Anne Tybjærg-Hansen, Peter Schnohr & Børge G Nordestgaard. (2014) Total and Cause-Specific Mortality by Moderately and Markedly Increased Ferritin Concentrations: General Population Study and Metaanalysis. Clinical Chemistry 60:11, pages 1419-1428.
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Bruna Leandro, Milena Paneque, Jorge Sequeiros & Graça Porto. (2014) Insufficient Referral for Genetic Counseling in the Management of Hereditary Haemochromatosis in Portugal: A Study of Perceptions of Health Professionals Requesting HFE Genotyping. Journal of Genetic Counseling 23:5, pages 770-777.
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F. Stickel, S. Buch, H. Zoller, R. Hultcrantz, S. Gallati, C. Osterreicher, A. Finkenstedt, A. Stadlmayr, E. Aigner, E. Sahinbegovic, C. Sarrazin, C. Schafmayer, F. Braun, W. Erhart, M. Nothnagel, M. M. Lerch, J. Mayerle, H. Volzke, A. Schaller, W. Kratzer, B. O. Boehm, B. Sipos, M. D'Amato, L. Torkvist, P. Stal, A. Arlt, A. Franke, T. Becker, M. Krawczak, J. Zwerina, T. Berg, H. Hinrichsen, E. Krones, C. Dejaco, M. Strasser, C. Datz & J. Hampe. (2014) Evaluation of genome-wide loci of iron metabolism in hereditary hemochromatosis identifies PCSK7 as a host risk factor of liver cirrhosis. Human Molecular Genetics 23:14, pages 3883-3890.
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Christina Ellervik, Thomas Mandrup-Poulsen, Anne Tybjærg-Hansen & Børge G. Nordestgaard. (2014) Total and Cause-Specific Mortality by Elevated Transferrin Saturation and Hemochromatosis Genotype in Individuals With Diabetes: Two General Population Studies. Diabetes Care 37:2, pages 444-452.
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Christina Ellervik, Henrik Ullits Andersen, Anne Tybjærg-Hansen, Merete Frandsen, Henrik Birgens, Børge G. Nordestgaard & Thomas Mandrup-Poulsen. (2013) Total Mortality by Elevated Transferrin Saturation in Patients With Diabetes. Diabetes Care 36:9, pages 2646-2654.
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Lasse T Krogsbøll, Karsten Juhl Jørgensen, Christian Grønhøj Larsen & Peter C Gøtzsche. (2012) General health checks in adults for reducing morbidity and mortality from disease. Cochrane Database of Systematic Reviews.
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