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There are 12362 results for: content related to: The HFE gene heterozygosis H63D: a cofactor for liver damage in patients with steatohepatitis? Epidemiological and clinical considerations

  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

  2. 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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    2009 International BioIron Society Meeting

    American Journal of Hematology

    Volume 84, Issue 8, August 2009, Pages: E236–E375,

    Version of Record online : 17 JUN 2009, DOI: 10.1002/ajh.21464

  4. 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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    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

  6. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in German patients with hereditary haemochromatosis

    European Journal of Immunogenetics

    Volume 27, Issue 3, June 2000, Pages: 129–134, R. Gottschalk, C. Seidl, S. Schilling, A. Braner, E. Seifried, D. Hoelzer and J. P. Kaltwasser

    Version of Record online : 25 DEC 2001, DOI: 10.1046/j.1365-2370.2000.00215.x

  7. 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

  8. 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

  9. 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

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    Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age

    International Journal of Cancer

    Volume 125, Issue 1, 1 July 2009, Pages: 78–83, Zumin Shi, Daniel Johnstone, Bente A. Talseth-Palmer, Tiffany-Jane Evans, Allan D. Spigelman, Claire Groombridge, Elizabeth A. Milward, John K. Olynyk, Janina Suchy, Grzegorz Kurzawski, Jan Lubinski and Rodney J. Scott

    Version of Record online : 3 FEB 2009, DOI: 10.1002/ijc.24304

  11. Are hereditary hemochromatosis mutations involved in Alzheimer disease?

    American Journal of Medical Genetics

    Volume 93, Issue 1, 3 July 2000, Pages: 58–66, Sharon Moalem, Maire E. Percy, David F. Andrews, Theo P.A. Kruck, Simon Wong, Arthur J. Dalton, Pankaj Mehta, Bettye Fedor and Andrew C. Warren

    Version of Record online : 12 JUN 2000, DOI: 10.1002/1096-8628(20000703)93:1<58::AID-AJMG10>3.0.CO;2-L

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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

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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 in patients with hereditary haemochromatosis in Sweden

    Journal of Internal Medicine

    Volume 243, Issue 3, March 1998, Pages: 203–208, Cardoso, Stål, Hagen, Cabeda, Cabeda, Esin, De Sousa and Hultcrantz

    Version of Record online : 9 OCT 2008, DOI: 10.1046/j.1365-2796.1998.00270.x

  15. Prevalence and clinical implications of HFE gene mutations (C282Y and H63D) in patients with chronic hepatitis B and C in Taiwan

    Liver International

    Volume 25, Issue 2, April 2005, Pages: 214–219, Yone-Han Mah, Jia-Horng Kao, Chun-Jen Liu, Chi-Ling Chen, Pei-Jer Chen, Ming-Yang Lai and Ding-Shinn Chen

    Version of Record online : 11 FEB 2005, DOI: 10.1111/j.1478-3231.2005.01055.x

  16. 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

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    BioIron Abstracts

    American Journal of Hematology

    Volume 88, Issue 5, May 2013, Pages: E5–E243,

    Version of Record online : 18 APR 2013, DOI: 10.1002/ajh.23453

  18. Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay

    Tissue Antigens

    Volume 78, Issue 3, September 2011, Pages: 171–177, S. P. Cardoso, R. Patel, C. Brown and C. Navarrete

    Version of Record online : 7 JUL 2011, DOI: 10.1111/j.1399-0039.2011.01736.x

  19. 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

  20. Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population

    Clinical Genetics

    Volume 65, Issue 4, April 2004, Pages: 317–321, MJ Kotze, JNP De Villiers, CSH Bouwens, L Warnich, MG Zaahl, S Van Der Merwe and C Oberkanins

    Version of Record online : 16 FEB 2004, DOI: 10.1111/j.1399-0004.2004.00222.x