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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

49 related items for PubMed ID: 10660484

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  • 5. Hereditary hypotransferrinemia can lead to elevated transferrin saturation and, when associated to HFE or HAMP mutations, to iron overload.
    Beaumont-Epinette MP, Delobel JB, Ropert M, Deugnier Y, Loréal O, Jouanolle AM, Brissot P, Bardou-Jacquet E.
    Blood Cells Mol Dis; 2015 Feb; 54(2):151-4. PubMed ID: 25486930
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  • 6. HFE mutation analysis in patients with hepatitis C virus with positive screening for iron overload.
    Remacha AF, Carrasco M, Sardá MP, Barceló MJ, Baiget M.
    Haematologica; 1999 Mar; 84(3):284-5. PubMed ID: 10189401
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  • 8. Screening for hemochromatosis.
    Crawford DH, Hickman P.
    Hepatology; 2000 May; 31(5):1192-3. PubMed ID: 10796897
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  • 9. Mutations of the HFE gene and the risk of hepatocellular carcinoma.
    Racchi O, Mangerini R, Rapezzi D, Gaetani GF, Nobile MT, Picciotto A, Ferraris AM.
    Blood Cells Mol Dis; 1999 May; 25(5-6):350-3. PubMed ID: 10660482
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  • 11. Hepatic iron overload in patients with chronic viral hepatitis: role of HFE gene mutations.
    Piperno A, Vergani A, Malosio I, Parma L, Fossati L, Ricci A, Bovo G, Boari G, Mancia G.
    Hepatology; 1998 Oct; 28(4):1105-9. PubMed ID: 9755249
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  • 12. Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.
    Gomez PS, Parks S, Ries R, Tran TC, Gomez PF, Press RD.
    Nat Genet; 1999 Nov; 23(3):272. PubMed ID: 10545944
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  • 15. [Hereditary hemochromatosis: biochemical and genetic diagnosis].
    Quintero E.
    Gastroenterol Hepatol; 1999 Feb; 22 Suppl 1():1-5. PubMed ID: 10085593
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  • 16. Transferrin saturation and mortality.
    Benyamin B, Montgomery GW, Martin NG, Whitfield JB.
    Clin Chem; 2011 Jun; 57(6):921-3; author reply 923. PubMed ID: 21343418
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  • 19. [Iron in the era of molecular biology].
    Deugnier Y, Moirand R, Brissot P, David V.
    Pathol Biol (Paris); 1999 Nov; 47(9):938-44. PubMed ID: 10609274
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  • 20. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
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