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Journal Abstract Search

1787 related items for PubMed ID: 16871764

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  • 2. HFE based re-evaluation of heterozygous hemochromatosis.
    Moirand R, Guyader D, Mendler MH, Jouanolle AM, Le Gall JY, David V, Brissot P, Deugnier Y.
    Am J Med Genet; 2002 Sep 01; 111(4):356-61. PubMed ID: 12210292
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  • 3. 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 Sep 01; 27(1):290-3. PubMed ID: 11358390
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  • 5. Screening for HFE and iron overload.
    Ombiga J, Adams LA, Tang K, Trinder D, Olynyk JK.
    Semin Liver Dis; 2005 Nov 01; 25(4):402-10. PubMed ID: 16315134
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  • 6. Population screening for hemochromatosis: a study in 5370 Spanish blood donors.
    Sánchez M, Villa M, Ingelmo M, Sanz C, Bruguera M, Ascaso C, Oliva R.
    J Hepatol; 2003 Jun 01; 38(6):745-50. PubMed ID: 12763366
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  • 7. HFE genotype in patients with hemochromatosis and other liver diseases.
    Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK.
    Ann Intern Med; 1999 Jun 15; 130(12):953-62. PubMed ID: 10383365
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  • 8. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G.
    Z Gastroenterol; 2003 Nov 15; 41(11):1069-76. PubMed ID: 14648375
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  • 14. 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 15; 114(2):474-84. PubMed ID: 11529872
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  • 15. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.
    Genet Mol Res; 2005 Mar 31; 4(1):31-8. PubMed ID: 15841433
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  • 17. Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
    Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.
    J Med Genet; 2005 May 31; 42(5):390-5. PubMed ID: 15863667
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  • 18. Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers.
    Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, Maxwell JD.
    Eur J Gastroenterol Hepatol; 2002 Mar 31; 14(3):223-9. PubMed ID: 11953685
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  • 20. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.
    Cassanelli S, Pignatti E, Montosi G, Garuti C, Mariano M, Campioli D, Carbonieri A, Baldini E, Pietrangelo A.
    J Hepatol; 2001 Apr 31; 34(4):523-8. PubMed ID: 11394651
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