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Journal Abstract Search

248 related items for PubMed ID: 11495086

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  • 2. 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; 114(2):474-84. PubMed ID: 11529872
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  • 4. 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; 27(1):290-3. PubMed ID: 11358390
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  • 5. C282Y and H63D mutations of HFE gene in patients with advanced alcoholic liver disease.
    Ropero Gradilla P, Villegas Martínez A, Fernández Arquero M, García-Agúndez JA, González Fernández FA, Benítez Rodríguez J, Díaz-Rubio M, de la Concha EG, Ladero Quesada JM.
    Rev Esp Enferm Dig; 2001 Mar; 93(3):156-63. PubMed ID: 11469076
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  • 6. Differential HFE allele expression in hemochromatosis heterozygotes.
    Rosmorduc O, Poupon R, Nion I, Wendum D, Feder J, Béréziat G, Hermelin B.
    Gastroenterology; 2000 Oct; 119(4):1075-86. PubMed ID: 11040194
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  • 7. HFE gene mutations, hepatic iron content, and histological severity in hepatitis C virus-induced chronic hepatitis.
    Ladero JM, Ropero P, Ortega L, Taxonera C, González FA, López-Alonso G, Briceño O, Rodríguez-Agulló JL, González L, Villegas A, Díaz-Rubio M.
    Rev Esp Enferm Dig; 2003 Dec; 95(12):829-36. PubMed ID: 14972004
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  • 8. 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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  • 9. Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy.
    Mahon NG, Coonar AS, Jeffery S, Coccolo F, Akiyu J, Zal B, Houlston R, Levin GE, Baboonian C, McKenna WJ.
    Heart; 2000 Nov; 84(5):541-7. PubMed ID: 11040018
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  • 11. HFE mutations and chronic hepatitis C: H63D and C282Y heterozygosity are independent risk factors for liver fibrosis and cirrhosis.
    Erhardt A, Maschner-Olberg A, Mellenthin C, Kappert G, Adams O, Donner A, Willers R, Niederau C, Häussinger D.
    J Hepatol; 2003 Mar; 38(3):335-42. PubMed ID: 12586300
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  • 12. HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls.
    de Juan D, Reta A, Castiella A, Pozueta J, Prada A, Cuadrado E.
    Eur J Hum Genet; 2001 Dec; 9(12):961-4. PubMed ID: 11840200
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  • 13. Prevalence and clinical significance of HFE gene mutations in patients with iron overload.
    Brandhagen DJ, Fairbanks VF, Baldus WP, Smith CI, Kruckeberg KE, Schaid DJ, Thibodeau SN.
    Am J Gastroenterol; 2000 Oct; 95(10):2910-4. PubMed ID: 11051367
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  • 14. HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.
    Acton RT, Barton JC.
    Genet Test; 2001 Oct; 5(4):299-306. PubMed ID: 11960574
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  • 17. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E, Cerani P, Rolandi V, Rovati A, Bergamaschi G.
    Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
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  • 18. HFE gene mutation (C282Y) and phenotypic expression among a hospitalised population in a high prevalence area of haemochromatosis.
    Distante S, Berg JP, Lande K, Haug E, Bell H.
    Gut; 2000 Oct; 47(4):575-9. PubMed ID: 10986220
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