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Journal Abstract Search

310 related items for PubMed ID: 17297430

  • 21. Contribution of different HFE genotypes to iron overload disease: a pooled analysis.
    Burke W, Imperatore G, McDonnell SM, Baron RC, Khoury MJ.
    Genet Med; 2000; 2(5):271-7. PubMed ID: 11399207
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  • 22. Individuals homozygous for the H63D mutation have significantly elevated iron indexes.
    Samarasena J, Winsor W, Lush R, Duggan P, Xie Y, Borgaonkar M.
    Dig Dis Sci; 2006 Apr; 51(4):803-7. PubMed ID: 16615007
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  • 23. Increased incidence of HFE C282Y mutations in patients with iron overload and hepatocellular carcinoma developed in non-cirrhotic liver.
    Blanc JF, De Ledinghen V, Bernard PH, de Verneuil H, Winnock M, Le Bail B, Carles J, Saric J, Balabaud C, Bioulac-Sage P.
    J Hepatol; 2000 May; 32(5):805-11. PubMed ID: 10845668
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  • 24. 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 May; 4(6):436-40. PubMed ID: 14671617
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  • 25. 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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  • 26. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun; 21(2):177-80. PubMed ID: 22720307
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  • 27. Significance of H63D homozygosity in a Basque population with hemochromatosis.
    Castiella A, Zapata E, de Juan MD, Otazua P, Fernandez J, Zubiaurre L, Arriola JA, Gipuzkoa Hemochromatosis Group.
    J Gastroenterol Hepatol; 2010 Jul; 25(7):1295-8. PubMed ID: 20594259
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  • 31. 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; 89(10):1161-7. PubMed ID: 15477198
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  • 35. 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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  • 37. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.
    Eur J Haematol; 2001 Aug; 67(2):110-8. PubMed ID: 11722599
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  • 40. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
    Vizzi E, Loureiro CL, Gerder M, de las Nieves Garcia-Casal M, Rodríguez-Larralde A, Gerace L, Ludert JE, Liprandi F, Pujol FH.
    Ann Hematol; 2005 Nov; 84(12):802-6. PubMed ID: 15995871
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