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Journal Abstract Search

202 related items for PubMed ID: 25486930

  • 1. 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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  • 4. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.
    Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
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  • 8. Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis.
    Valenti L, Pulixi EA, Arosio P, Cremonesi L, Biasiotto G, Dongiovanni P, Maggioni M, Fargion S, Fracanzani AL.
    Haematologica; 2007 Aug; 92(8):1037-42. PubMed ID: 17640859
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  • 10. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.
    Gene; 2012 Oct 15; 508(1):15-20. PubMed ID: 22890139
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  • 13. Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.
    Lee PL, Halloran C, West C, Beutler E.
    Blood Cells Mol Dis; 2001 Oct 15; 27(1):285-9. PubMed ID: 11358389
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  • 15. Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis.
    Nicolas G, Viatte L, Lou DQ, Bennoun M, Beaumont C, Kahn A, Andrews NC, Vaulont S.
    Nat Genet; 2003 May 15; 34(1):97-101. PubMed ID: 12704388
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  • 18. 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 May 15; 27(1):290-3. PubMed ID: 11358390
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  • 20. Iron status and HFE genotype in erythrocyte pyruvate kinase deficiency: study of Italian cases.
    Zanella A, Bianchi P, Iurlo A, Boschetti C, Taioli E, Vercellati C, Zappa M, Fermo E, Tavazzi D, Sampietro M.
    Blood Cells Mol Dis; 2001 May 15; 27(3):653-61. PubMed ID: 11482880
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