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Journal Abstract Search

214 related items for PubMed ID: 20583211

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  • 4. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
    Warne CD, Zaloumis SG, Bertalli NA, Delatycki MB, Nicoll AJ, McLaren CE, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Allen KJ, Gurrin LC, HealthIron Study Investigators.
    J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
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  • 6. Thyroid-stimulating hormone and free thyroxine levels in persons with HFE C282Y homozygosity, a common hemochromatosis genotype: the HEIRS study.
    Barton JC, Leiendecker-Foster C, Reboussin DM, Adams PC, Acton RT, Eckfeldt JH, Hemochromatosis and Iron Overload Screening Study Research Investigators.
    Thyroid; 2008 Aug; 18(8):831-8. PubMed ID: 18651828
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  • 7. Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening.
    McLaren GD, McLaren CE, Adams PC, Barton JC, Reboussin DM, Gordeuk VR, Acton RT, Harris EL, Speechley MR, Sholinsky P, Dawkins FW, Snively BM, Vogt TM, Eckfeldt JH, Hemochromatosis and Iron Overload Screen (HEIRS) Study Research Investigators.
    Can J Gastroenterol; 2008 Nov; 22(11):923-30. PubMed ID: 19018338
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  • 10. 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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  • 11. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186
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  • 12. A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.
    Constantine CC, Anderson GJ, Vulpe CD, McLaren CE, Bahlo M, Yeap HL, Gertig DM, Osborne NJ, Bertalli NA, Beckman KB, Chen V, Matak P, McKie AT, Delatycki MB, Olynyk JK, English DR, Southey MC, Giles GG, Hopper JL, Allen KJ, Gurrin LC.
    Br J Haematol; 2009 Oct 28; 147(1):140-9. PubMed ID: 19673882
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  • 13. HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.
    Adams PC, McLaren CE, Speechley M, McLaren GD, Barton JC, Eckfeldt JH.
    Can J Gastroenterol; 2013 Jul 28; 27(7):390-2. PubMed ID: 23862168
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  • 16. Prevalence and characteristics of anti-HCV positivity and chronic hepatitis C virus infection in HFE p.C282Y homozygotes.
    Barton JC, Barton JC, Adams PC.
    Ann Hepatol; 2019 Jul 28; 18(2):354-359. PubMed ID: 31056361
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  • 17. Prevalence of hemochromatosis-related symptoms among individuals with mutations in the HFE gene.
    Waalen J, Felitti V, Gelbart T, Ho NJ, Beutler E.
    Mayo Clin Proc; 2002 Jun 28; 77(6):522-30. PubMed ID: 12059121
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  • 19. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct 28; 70(4):294-300. PubMed ID: 17767550
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