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Journal Abstract Search

383 related items for PubMed ID: 12482402

  • 1. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.
    Phatak PD, Ryan DH, Cappuccio J, Oakes D, Braggins C, Provenzano K, Eberly S, Sham RL.
    Blood Cells Mol Dis; 2002; 29(1):41-7. PubMed ID: 12482402
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  • 2. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.
    Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.
    Hematol J; 2003; 4(6):436-40. PubMed ID: 14671617
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  • 8. HFE genotype in patients with hemochromatosis and other liver diseases.
    Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK.
    Ann Intern Med; 1999 Jun 15; 130(12):953-62. PubMed ID: 10383365
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  • 9. Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.
    De Gobbi M, D'Antico S, Castagno F, Testa D, Merlini R, Bondi A, Camaschella C.
    Haematologica; 2004 Oct 15; 89(10):1161-7. PubMed ID: 15477198
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  • 10. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.
    Br J Haematol; 2001 Aug 15; 114(2):474-84. PubMed ID: 11529872
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  • 12. 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 Aug 15; 62(7):527-35. PubMed ID: 12512743
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  • 13. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Aug 15; 27(1):290-3. PubMed ID: 11358390
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  • 15. Expression of the HFE hemochromatosis gene in a community-based population of elderly women.
    Rossi E, Kuek C, Beilby JP, Jeffrey GP, Devine A, Prince RL.
    J Gastroenterol Hepatol; 2004 Oct 15; 19(10):1150-4. PubMed ID: 15377292
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  • 16. Natural history of HFE simple heterozygosity for C282Y and H63D: a prospective 12-year study.
    Zaloumis SG, Allen KJ, Bertalli NA, Turkovic L, Delatycki MB, Nicoll AJ, McLaren CE, English DR, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Gurrin LC, HealthIron Study Investigators.
    J Gastroenterol Hepatol; 2015 Apr 15; 30(4):719-25. PubMed ID: 25311314
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  • 18. HFE gene mutations an Apulian population: allele frequencies.
    Pietrapertosa A, Vitucci A, Campanale D, Palma A, Renni R, Delios G, Tannoia N.
    Eur J Epidemiol; 2003 Apr 15; 18(7):685-9. PubMed ID: 12952143
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  • 19. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun 15; 27(3):129-34. PubMed ID: 10940080
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  • 20. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
    Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK.
    Gastroenterology; 2002 Mar 15; 122(3):646-51. PubMed ID: 11874997
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