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Journal Abstract Search

145 related items for PubMed ID: 12714263

  • 21. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr; 47(5):404-10. PubMed ID: 9510559
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  • 22. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2011 Apr 15; 46(4):302-7. PubMed ID: 21411349
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  • 23. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
    Njajou OT, Houwing-Duistermaat JJ, Osborne RH, Vaessen N, Vergeer J, Heeringa J, Pols HA, Hofman A, van Duijn CM.
    Eur J Hum Genet; 2003 Mar 15; 11(3):225-31. PubMed ID: 12673276
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  • 24. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ.
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr 15; 30(4):223-8. PubMed ID: 19731820
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  • 25. Primary osteoarthritis in the ankle joint is associated with finger metacarpophalangeal osteoarthritis and the H63D mutation in the HFE gene: evidence for a hemochromatosis-like polyarticular osteoarthritis phenotype.
    Carroll GJ.
    J Clin Rheumatol; 2006 Jun 15; 12(3):109-13. PubMed ID: 16755236
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  • 26. Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
    Hannuksela J, Leppilampi M, Peuhkurinen K, Kärkkäinen S, Saastamoinen E, Heliö T, Kaartinen M, Nieminen MS, Nieminen P, Parkkila S.
    Eur J Heart Fail; 2005 Jan 15; 7(1):103-8. PubMed ID: 15642540
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  • 27. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL, Palácios SA, Couto CA, Cançado EL, Carrilho FJ, Laudanna AA, Kalil J, Gayotto LC, Goldberg AC.
    Braz J Med Biol Res; 2002 Mar 15; 35(3):329-35. PubMed ID: 11887210
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  • 29. Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.
    Wallace DF, Walker AP, Pietrangelo A, Clare M, Bomford AB, Dixon JL, Powell LW, Subramaniam VN, Dooley JS.
    J Hepatol; 2002 Apr 15; 36(4):474-9. PubMed ID: 11943417
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  • 33. Frequencies of the haemochromatosis gene (HFE) variants C282Y, H63D and S65C in 6,020 ethnic Danish men.
    Pedersen P, Melsen GV, Milman N.
    Ann Hematol; 2008 Sep 15; 87(9):735-40. PubMed ID: 18542962
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  • 36. Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia.
    Rodríguez-López R, Donoso M, Fernández-Cavada M, González LM, Margallo A, Corral C, Gallego M, García de Cáceres MT, Herrera T, González C, Vagace JM, Gervasini G.
    Gene; 2013 Feb 01; 514(1):31-5. PubMed ID: 23178241
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  • 37. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.
    Scand J Clin Lab Invest; 2002 Feb 01; 62(7):527-35. PubMed ID: 12512743
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  • 39. The H63D mutation of the hemochromatosis gene is associated with sustained virological response in chronic hepatitis C patients treated with interferon-based therapy: a meta-analysis.
    Li SH, Zhao H, Ren YY, Liu YZ, Song G, Ding P, Ding YP, Wang GQ.
    Tohoku J Exp Med; 2012 Apr 01; 226(4):293-9. PubMed ID: 22499121
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  • 40. Frequencies of C282Y and H63D mutations and transferrin saturation indices in the Korean population.
    Choi SJ, Min WK, Chun S, Park H, Kim JW, Park CJ, Chi HS.
    Clin Chem Lab Med; 2002 Jul 01; 40(7):689-92. PubMed ID: 12241015
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