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Journal Abstract Search

95 related items for PubMed ID: 9328324

  • 1. Clinical and family studies in genetic hemochromatosis: microsatellite and HFE studies in five atypical families.
    Adams PC, Campion ML, Gandon G, LeGall JY, David V, Jouanolle AM.
    Hepatology; 1997 Oct; 26(4):986-90. PubMed ID: 9328324
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  • 2. 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; 88(8):775-84. PubMed ID: 19159930
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  • 6. Unsaturated iron binding capacity and transferrin saturation are equally reliable in detection of HFE hemochromatosis.
    Murtagh LJ, Whiley M, Wilson S, Tran H, Bassett ML.
    Am J Gastroenterol; 2002 Aug; 97(8):2093-9. PubMed ID: 12190182
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  • 8. Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.
    Crawford DH, Jazwinska EC, Cullen LM, Powell LW.
    Gastroenterology; 1998 May; 114(5):1003-8. PubMed ID: 9558290
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  • 9. Disease-related conditions in relatives of patients with hemochromatosis.
    Bulaj ZJ, Ajioka RS, Phillips JD, LaSalle BA, Jorde LB, Griffen LM, Edwards CQ, Kushner JP.
    N Engl J Med; 2000 Nov 23; 343(21):1529-35. PubMed ID: 11087882
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  • 10. The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda.
    Roberts AG, Whatley SD, Nicklin S, Worwood M, Pointon JJ, Stone C, Elder GH.
    Hepatology; 1997 Jan 23; 25(1):159-61. PubMed ID: 8985283
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  • 11. Screening for hereditary haemochromatosis.
    Nadakkavukaran IM, Gan EK, Olynyk JK.
    Pathology; 2012 Feb 23; 44(2):148-52. PubMed ID: 22198253
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  • 12. Hemochromatosis: association of severity of iron overload with genetic markers.
    Barton JC, Harmon L, Rivers C, Acton RT.
    Blood Cells Mol Dis; 1996 Feb 23; 22(3):195-204. PubMed ID: 9075570
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  • 13. The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis.
    Adams PC, Deugnier Y, Moirand R, Brissot P.
    Hepatology; 1997 Jan 23; 25(1):162-6. PubMed ID: 8985284
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  • 15. Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden.
    Olsson KS, Konar J, Dufva IH, Ricksten A, Raha-Chowdhury R.
    Eur J Haematol; 2011 Jan 23; 86(1):75-82. PubMed ID: 20946107
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  • 17. Idiopathic hemochromatosis: a study of biochemical expression in 247 heterozygous members of 63 families: evidence for a single major HLA-linked gene.
    Simon M, Fauchet R, Hespel JP, Beaumont C, Brissot P, Hery B, Hita De Nercy Y, Genetet B, Bourel M.
    Gastroenterology; 1980 Apr 23; 78(4):703-8. PubMed ID: 7353757
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