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Journal Abstract Search


904 related items for PubMed ID: 16476869

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  • 3. The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosis.
    Adams LA, Angulo P, Abraham SC, Torgerson H, Brandhagen D.
    Liver Int; 2006 Apr; 26(3):298-304. PubMed ID: 16584391
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  • 4. Is there a threshold of hepatic iron concentration that leads to cirrhosis in C282Y hemochromatosis?
    Adams PC.
    Am J Gastroenterol; 2001 Feb; 96(2):567-9. PubMed ID: 11232708
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  • 8. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry.
    Kowdley KV, Brandhagen DJ, Gish RG, Bass NM, Weinstein J, Schilsky ML, Fontana RJ, McCashland T, Cotler SJ, Bacon BR, Keeffe EB, Gordon F, Polissar N, National Hemochromatosis Transplant Registry.
    Gastroenterology; 2005 Aug; 129(2):494-503. PubMed ID: 16083706
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  • 10. Clinical aspects of hemochromatosis.
    O'Neil J, Powell L.
    Semin Liver Dis; 2005 Nov; 25(4):381-91. PubMed ID: 16315132
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  • 14. [Iron storage disease].
    Horváth G, Dávid K.
    Orv Hetil; 2004 Sep 26; 145(39):1979-84. PubMed ID: 15553908
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  • 15. [Hemochromatosis--from an underdiagnosed curiosity to a common disease].
    Hagve TA, Asberg A, Ulvik R, Borch-Iohnsen B, Thorstensen K.
    Tidsskr Nor Laegeforen; 2009 Apr 30; 129(9):863-6. PubMed ID: 19415085
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  • 16. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects.
    Cruz E, Melo G, Lacerda R, Almeida S, Porto G.
    Blood Cells Mol Dis; 2006 Apr 30; 37(1):33-9. PubMed ID: 16762569
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  • 17. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation.
    Shaheen NJ, Bacon BR, Grimm IS.
    Hepatology; 1998 Aug 30; 28(2):526-9. PubMed ID: 9696020
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  • 18. Patient compliance with phlebotomy therapy for iron overload associated with hemochromatosis.
    Hicken BL, Tucker DC, Barton JC.
    Am J Gastroenterol; 2003 Sep 30; 98(9):2072-7. PubMed ID: 14499790
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  • 20. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C, Opazo S, Murga MJ, Martínez-Castro P.
    Eur J Haematol; 2007 Jan 30; 78(1):66-71. PubMed ID: 17042772
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