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Journal Abstract Search

166 related items for PubMed ID: 20031587

  • 1. Letter by Sullivan regarding article, "HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: the hemochromatosis and iron overload screening study".
    Sullivan JL.
    Circ Cardiovasc Genet; 2009 Jun; 2(3):e1. PubMed ID: 20031587
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  • 2. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH.
    Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565
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  • 3. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
    Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    Genet Test; 2007 Feb; 11(3):269-75. PubMed ID: 17949288
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  • 4. HFE hemochromatosis: influence of dietary iron intake on the iron overload of C282Y homozygous patients.
    Saliou P, Le Gac G, Mérour MC, Tripogney C, Chanu B, Gourlaouen I, Nousbaum JB, Férec C, Scotet V.
    Ann Hematol; 2015 Jul; 94(7):1225-7. PubMed ID: 25740382
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  • 8. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC, Wiener HW, Acton RT, Go RC.
    Blood Cells Mol Dis; 2005 Jul; 34(1):38-47. PubMed ID: 15607698
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  • 9. Serial serum ferritin measurements in untreated HFE C282Y homozygotes in the Hemochromatosis and Iron Overload Screening Study.
    Adams PC, Reboussin DM, Barton JC, Acton RT, Speechley M, Leiendecker-Foster C, Meenan R, Passmore L, McLaren CE, McLaren GD, Gordeuk V, Dawkins F, Eckfeldt JH.
    Int J Lab Hematol; 2008 Aug; 30(4):300-5. PubMed ID: 18665827
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  • 12. Multifactorial iron man.
    Robson KJ, Drakesmith H.
    Digestion; 2005 Aug; 72(1):22-4. PubMed ID: 16103672
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  • 13. Hereditary hemochromatosis--a new look at an old disease.
    Pietrangelo A.
    N Engl J Med; 2004 Jun 03; 350(23):2383-97. PubMed ID: 15175440
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  • 14. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
    Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ.
    Hum Mol Genet; 2003 Sep 01; 12(17):2241-7. PubMed ID: 12915468
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  • 15. Serum hepcidin levels are innately low in HFE-related haemochromatosis but differ between C282Y-homozygotes with elevated and normal ferritin levels.
    van Dijk BA, Laarakkers CM, Klaver SM, Jacobs EM, van Tits LJ, Janssen MC, Swinkels DW.
    Br J Haematol; 2008 Sep 01; 142(6):979-85. PubMed ID: 18557745
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  • 17. Regulatory defects in liver and intestine implicate abnormal hepcidin and Cybrd1 expression in mouse hemochromatosis.
    Muckenthaler M, Roy CN, Custodio AO, Miñana B, deGraaf J, Montross LK, Andrews NC, Hentze MW.
    Nat Genet; 2003 May 01; 34(1):102-7. PubMed ID: 12704390
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