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Journal Abstract Search

127 related items for PubMed ID: 11113655

  • 1. Biochemical expression of heterozygous hereditary hemochromatosis.
    de Valk B, Witlox RS, van der Schouw YT, Marx JJ.
    Eur J Intern Med; 2000 Dec 20; 11(6):317-321. PubMed ID: 11113655
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  • 2. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun 20; 27(3):129-34. PubMed ID: 10940080
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  • 3. 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 20; 41(11):1069-76. PubMed ID: 14648375
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  • 4. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186
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  • 5. 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 28; 114(2):474-84. PubMed ID: 11529872
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  • 6. Compound heterozygous hemochromatosis genotype predicts increased iron and erythrocyte indices in women.
    Rossi E, Olynyk JK, Cullen DJ, Papadopoulos G, Bulsara M, Summerville L, Powell LW.
    Clin Chem; 2000 Feb 28; 46(2):162-6. PubMed ID: 10657371
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  • 7. 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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  • 8. 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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  • 9. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P, Milman N.
    Ann Hematol; 2009 Aug 15; 88(8):775-84. PubMed ID: 19159930
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  • 10. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 15; 52(6):602-8. PubMed ID: 16871764
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  • 11. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.
    Scand J Clin Lab Invest; 2002 Jun 15; 62(7):527-35. PubMed ID: 12512743
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  • 14. 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 15; 38(6):745-50. PubMed ID: 12763366
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  • 18. Genotype screening for hereditary hemochromatosis among voluntary blood donors in Hungary.
    Andrikovics H, Kalmár L, Bors A, Fandl B, Petri I, Kalász L, Tordai A.
    Blood Cells Mol Dis; 2001 Jun 15; 27(1):334-41. PubMed ID: 11358395
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  • 19. 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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