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There are 1834 results for: content related to: Hemochromatosis genotypes and risk of 31 disease endpoints: Meta-analyses including 66,000 cases and 226,000 controls

  1. 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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    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

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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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    Haemochromatosis genotype and iron overload: association with hypertension and left ventricular hypertrophy

    Journal of Internal Medicine

    Volume 268, Issue 3, September 2010, Pages: 252–264, C. Ellervik, A. Tybjærg-Hansen, M. Appleyard, H. Ibsen and B. G. Nordestgaard

    Version of Record online : 29 JAN 2010, DOI: 10.1111/j.1365-2796.2010.02217.x

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    Risk of cancer by transferrin saturation levels and haemochromatosis genotype: population-based study and meta-analysis

    Journal of Internal Medicine

    Volume 271, Issue 1, January 2012, Pages: 51–63, C. Ellervik, A. Tybjærg-Hansen and B. G. Nordestgaard

    Version of Record online : 16 JUN 2011, DOI: 10.1111/j.1365-2796.2011.02404.x

  6. Distribution of HFE C282Y and H63D mutations in the Balearic Islands (NE Spain)

    Clinical Genetics

    Volume 61, Issue 1, January 2002, Pages: 43–48, P Guix, A Picornell, M Parera, A Galmes, A Obrador, MM Ramon and JA Castro

    Version of Record online : 19 MAR 2002, DOI: 10.1034/j.1399-0004.2002.610109.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

  8. 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

  9. Hepatic iron loading in patients with compound heterozygous HFE mutations

    Liver International

    Volume 24, Issue 6, December 2004, Pages: 631–636, Ee Mun Lim, Enrico Rossi, W. Bastiaan De Boer, William D. Reed and Gary P. Jeffrey

    Version of Record online : 26 NOV 2004, DOI: 10.1111/j.1478-3231.2004.0953.x

  10. Hemochromatosis mutations C282Y and H63D in ‘cis’ phase

    Clinical Genetics

    Volume 60, Issue 1, July 2001, Pages: 68–72, LG Best, PE Harris and EL Spriggs

    Version of Record online : 20 DEC 2001, DOI: 10.1034/j.1399-0004.2001.600111.x

  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 homozygotes are at increased risk of breast and colorectal cancer

    Hepatology

    Volume 51, Issue 4, April 2010, Pages: 1311–1318, Nicholas J. Osborne, Lyle C. Gurrin, Katrina J. Allen, Clare C. Constantine, Martin B. Delatycki, Christine E. McLaren, Dorota M. Gertig, Gregory J. Anderson, Melissa C. Southey, John K. Olynyk, Lawrie W. Powell, John L. Hopper, Graham G. Giles and Dallas R. English

    Version of Record online : 30 NOV 2009, DOI: 10.1002/hep.23448

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    HFE polymorphisms influence the response to chemotherapeutic agents via induction of p16INK4A

    International Journal of Cancer

    Volume 129, Issue 9, 1 November 2011, Pages: 2104–2114, Sang Y. Lee, Siying Liu, Ryan M. Mitchell, Becky Slagle-Webb, Young-Soo Hong, Jonas M. Sheehan and James R. Connor

    Version of Record online : 7 APR 2011, DOI: 10.1002/ijc.25888

  14. Highly sensitivity adhesion molecules detection in hereditary haemochromatosis patients reveals altered expression

    International Journal of Immunogenetics

    Volume 37, Issue 2, April 2010, Pages: 125–133, S. Norris, M. White, A. K. Mankan and M. W. Lawless

    Version of Record online : 19 FEB 2010, DOI: 10.1111/j.1744-313X.2010.00904.x

  15. 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

  16. 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

  17. Expression of the HFE hemochromatosis gene in a community-based population of elderly women

    Journal of Gastroenterology and Hepatology

    Volume 19, Issue 10, October 2004, Pages: 1150–1154, ENRICO ROSSI, CONCHITA KUEK, JOHN P BEILBY, GARY P JEFFREY, AMANDA DEVINE and RICHARD L PRINCE

    Version of Record online : 3 JUN 2004, DOI: 10.1111/j.1440-1746.2004.03436.x

  18. Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosity

    Clinical Genetics

    Volume 69, Issue 2, February 2006, Pages: 155–162, M Matas, P Guix, JA Castro, M Parera, MM Ramon, A Obrador and A Picornell

    Version of Record online : 4 JAN 2006, DOI: 10.1111/j.1399-0004.2005.00563.x

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    Haemochromatosis mutations in North-East Scotland

    British Journal of Haematology

    Volume 106, Issue 2, August 1999, Pages: 385–387, Z. Miedzybrodzka, S. Loughlin, D. Baty, A. Terron, K. Kelly, J. Dean, M. Greaves, M. Pippard and N. Haites

    Version of Record online : 5 APR 2002, DOI: 10.1046/j.1365-2141.1999.01554.x

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    The evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic

    American Journal of Physical Anthropology

    Volume 160, Issue 1, May 2016, Pages: 86–101, Kathleen M. Heath, Jacob H. Axton, John M. McCullough and Nathan Harris

    Version of Record online : 22 JAN 2016, DOI: 10.1002/ajpa.22937