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There are 3636 results for: content related to: Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age

  1. You have free access to this content
    Lower serum hepcidin and greater parenchymal iron in nonalcoholic fatty liver disease patients with C282Y HFE mutations

    Hepatology

    Volume 56, Issue 5, November 2012, Pages: 1730–1740, James E. Nelson, Elizabeth M. Brunt, Kris V. Kowdley and for the Nonalcoholic Steatohepatitis Clinical Research Network

    Version of Record online : 20 SEP 2012, DOI: 10.1002/hep.25856

  2. Natural history of HFE simple heterozygosity for C282Y and H63D: A prospective 12-year study

    Journal of Gastroenterology and Hepatology

    Volume 30, Issue 4, April 2015, Pages: 719–725, Sophie G Zaloumis, Katrina J Allen, Nadine A Bertalli, Lidija Turkovic, Martin B Delatycki, Amanda J Nicoll, Christine E McLaren, Dallas R English, John L Hopper, Graham G Giles, Gregory J Anderson, John K Olynyk, Lawrie W Powell, Lyle C Gurrin and for theHealthIron Study Investigators

    Version of Record online : 16 MAR 2015, DOI: 10.1111/jgh.12804

  3. Population-based study of cystic fibrosis disease severity and haemochromatosis gene mutations

    Respirology

    Volume 15, Issue 1, January 2010, Pages: 141–149, Upasna PRATAP, Stephen QUINN, Leigh B. BLIZZARD and David W. REID

    Version of Record online : 27 DEC 2009, DOI: 10.1111/j.1440-1843.2009.01649.x

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    Targeted screening for hereditary haemochromatosis in high-risk groups

    Alimentary Pharmacology & Therapeutics

    Volume 20, Issue 1, July 2004, Pages: 1–14, S. DuBois and K. V. Kowdley

    Version of Record online : 21 JUN 2004, DOI: 10.1111/j.1365-2036.2004.02024.x

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    HFE Cys282Tyr homozygotes with serum ferritin concentrations below 1000 μg/L are at low risk of hemochromatosis

    Hepatology

    Volume 52, Issue 3, September 2010, Pages: 925–933, Katrina J. Allen, Nadine A. Bertalli, Nicholas J. Osborne, Clare C. Constantine, Martin B. Delatycki, Amy E. Nisselle, Amanda J. Nicoll, Dorota M. Gertig, Christine E. McLaren, Graham G. Giles, John L. Hopper, Gregory J. Anderson, John K. Olynyk, Lawrie W. Powell, Lyle C. Gurrin and for the HealthIron Study Investigators

    Version of Record online : 1 JUN 2010, DOI: 10.1002/hep.23786

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    HFE-associated hereditary hemochromatosis: Overview of genetics and clinical implications for nurse practitioners in primary care settings

    Journal of the American Association of Nurse Practitioners

    Volume 26, Issue 3, March 2014, Pages: 113–122, Donna Emanuele, Ivy Tuason and Quannetta T. Edwards

    Version of Record online : 5 FEB 2014, DOI: 10.1002/2327-6924.12106

  7. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women

    Journal of Gastroenterology and Hepatology

    Volume 32, Issue 4, April 2017, Pages: 797–802, Charles D Warne, Sophie G Zaloumis, Nadine A Bertalli, Martin B Delatycki, Amanda J Nicoll, Christine E McLaren, John L Hopper, Graham G Giles, Greg J Anderson, John K Olynyk, Lawrie W Powell, Katrina J Allen, Lyle C Gurrin and for the HealthIron Study Investigators

    Version of Record online : 24 MAR 2017, DOI: 10.1111/jgh.13621

  8. HFE, the MHC and hemochromatosis: Paradigm for an extended function for MHC class I

    Tissue Antigens

    Volume 61, Issue 4, April 2003, Pages: 263–275, C.S. Cardoso and M. De Sousa

    Version of Record online : 7 MAY 2003, DOI: 10.1034/j.1399-0039.2003.00065.x

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    Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry

    British Journal of Haematology

    Volume 120, Issue 5, March 2003, Pages: 887–893, Ernest Beutler, Vincent Felitti, Terri Gelbart and Jill Waalen

    Version of Record online : 3 MAR 2003, DOI: 10.1046/j.1365-2141.2003.04215.x

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    Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy

    European Journal of Heart Failure

    Volume 7, Issue 1, January 2005, Pages: 103–108, Jokke Hannuksela, Mari Leppilampi, Keijo Peuhkurinen, Satu Kärkkäinen, Eija Saastamoinen, Tiina Heliö, Maija Kaartinen, Markku S. Nieminen, Pentti Nieminen and Seppo Parkkila

    Version of Record online : 11 JAN 2005, DOI: 10.1016/j.ejheart.2004.03.007

  11. Significance of H63D homozygosity in a Basque population with hemochromatosis

    Journal of Gastroenterology and Hepatology

    Volume 25, Issue 7, July 2010, Pages: 1295–1298, Agustin Castiella, Eva Zapata, Maria Dolores De Juan, Pedro Otazua, Javier Fernandez, Leire Zubiaurre and Jose A. Arriola

    Version of Record online : 23 JUN 2010, DOI: 10.1111/j.1440-1746.2010.06247.x

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    HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity

    Hepatology

    Volume 50, Issue 1, July 2009, Pages: 94–101, Lyle C. Gurrin, Nadine A. Bertalli, Gregory W. Dalton, Nicholas J. Osborne, Clare C. Constantine, Christine E. McLaren, Dallas R. English, Dorota M. Gertig, Martin B. Delatycki, Amanda J. Nicoll, Melissa C. Southey, John L. Hopper, Graham G. Giles, Gregory J. Anderson, John K. Olynyk, Lawrie W. Powell, Katrina J. Allen and HealthIron Study Investigators

    Version of Record online : 19 MAR 2009, DOI: 10.1002/hep.22972

  13. Analysis of HFE Genes C282Y, H63D, and S65D in Patients With Hyperferritinemia From Northeastern Brazil

    Journal of Clinical Laboratory Analysis

    Volume 28, Issue 3, May 2014, Pages: 178–185, Gioconda Dias Rodrigues Leão, Juliana Mendonça Freire, Andrea Luciana Araújo Cunha Fernandes, Taissa Maria Moura de Oliveira, Nilma Dias Leão, Erica Aires Gil, Roberto Chaves de Vasconcelos, João Paulo da Silva Azevedo, Valéria Soraya de Farias Sales, Telma Maria de Araújo Moura Lemos, Marcos Dias Leão, Francisco Fernandes do Nascimento Jr, James Farley Rafael Maciel, Rodrigo Villar de Freitas, Aldair de Souza Paiva and Geraldo Barroso Cavalcanti Jr.

    Version of Record online : 6 JAN 2014, DOI: 10.1002/jcla.21663

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    HFE C282Y mutations are associated with advanced hepatic fibrosis in Caucasians with nonalcoholic steatohepatitis

    Hepatology

    Volume 46, Issue 3, September 2007, Pages: 723–729, James E. Nelson, Renuka Bhattacharya, Keith D. Lindor, Naga Chalasani, Stuart Raaka, E. Jenny Heathcote, Emil Miskovsky, Eldon Shaffer, Stephen J. Rulyak and Kris V. Kowdley

    Version of Record online : 6 AUG 2007, DOI: 10.1002/hep.21742

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    Haemochromatosis in patients with β-thalassaemia trait

    British Journal of Haematology

    Volume 111, Issue 3, December 2000, Pages: 908–914, Alberto Piperno, Raffaella Mariani, Cristina Arosio, Anna Vergani, Sandra Bosio, Silvia Fargion, Maurizio Sampietro, Domenico Girelli, Mirella Fraquelli, Dario Conte, Gemino Fiorelli and Clara Camaschella

    Version of Record online : 2 AUG 2008, DOI: 10.1111/j.1365-2141.2000.02436.x

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    HFE mutations, iron deficiency and overload in 10 500 blood donors

    British Journal of Haematology

    Volume 114, Issue 2, August 2001, Pages: 474–484, H. A. Jackson, K. Carter, C. Darke, M. G. Guttridge, D. Ravine, R. D. Hutton, J. A. Napier and M. Worwood

    Version of Record online : 20 DEC 2001, DOI: 10.1046/j.1365-2141.2001.02949.x

  17. A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans

    International Journal of Immunogenetics

    Volume 34, Issue 5, October 2007, Pages: 359–367, J. Vieira, C. S. Cardoso, J. Pinto, K. Patil, P. Brazdil, E. Cruz, C. Mascarenhas, R. Lacerda, A. Gartner, S. Almeida, H. Alves and G. Porto

    Version of Record online : 18 JUN 2007, DOI: 10.1111/j.1744-313X.2007.00700.x

  18. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population

    Tissue Antigens

    Volume 70, Issue 3, September 2007, Pages: 252–255, A. Lin, W. H. Yan, H. H. Xu, M. Zhu and M. Y. Zhou

    Version of Record online : 15 JUN 2007, DOI: 10.1111/j.1399-0039.2007.00877.x

  19. Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in Native Americans and whites in the Hemochromatosis and Iron Overload Screening Study

    Clinical Genetics

    Volume 69, Issue 1, January 2006, Pages: 48–57, JC Barton, RT Acton, L Lovato, MR Speechley, CE McLaren, EL Harris, DM Reboussin, PC Adams, FW Dawkins, VR Gordeuk, AP Walker and for the Hemochromatosis and Iron Overload Screening Study Research Investigators

    Version of Record online : 13 DEC 2005, DOI: 10.1111/j.1399-0004.2006.00553.x

  20. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis

    Tissue Antigens

    Volume 70, Issue 4, October 2007, Pages: 294–300, M. W. Lawless, M. White, A. K. Mankan, M. J. O’Dwyer and S. Norris

    Version of Record online : 16 JUL 2007, DOI: 10.1111/j.1399-0039.2007.00895.x