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Journal Abstract Search

1234 related items for PubMed ID: 9410475

  • 1. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
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  • 4. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
    Brissot P, Moirand R, Jouanolle AM, Guyader D, Le Gall JY, Deugnier Y, David V.
    J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
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  • 6. 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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  • 7. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb 15; 26(1):2-8. PubMed ID: 10772870
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  • 11. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.
    N Engl J Med; 1999 Sep 02; 341(10):718-24. PubMed ID: 10471457
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  • 12. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis.
    Walsh A, Dixon JL, Ramm GA, Hewett DG, Lincoln DJ, Anderson GJ, Subramaniam VN, Dodemaide J, Cavanaugh JA, Bassett ML, Powell LW.
    Clin Gastroenterol Hepatol; 2006 Nov 02; 4(11):1403-10. PubMed ID: 16979952
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  • 13. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
    Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK.
    Gastroenterology; 2002 Mar 02; 122(3):646-51. PubMed ID: 11874997
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  • 14. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD, Flora K, Gross C, Rabkin JM, Corless CL.
    Am J Clin Pathol; 1998 May 02; 109(5):577-84. PubMed ID: 9576576
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  • 15. 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 02; 114(2):474-84. PubMed ID: 11529872
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  • 16. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.
    Eur J Haematol; 2001 Aug 02; 67(2):110-8. PubMed ID: 11722599
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  • 17. 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 02; 41(11):1069-76. PubMed ID: 14648375
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  • 18. Relation between HFE mutations and mild iron-overload expression.
    Mura C, Le Gac G, Raguénes O, Mercier AY, Le Guen A, Férec C.
    Mol Genet Metab; 2000 Apr 02; 69(4):295-301. PubMed ID: 10870847
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  • 19. 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 02; 95(10):2910-4. PubMed ID: 11051367
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  • 20. Differences in hepatic phenotype between hemochromatosis patients with HFE C282Y homozygosity and other HFE genotypes.
    Cheng R, Barton JC, Morrison ED, Phatak PD, Krawitt EL, Gordon SC, Kowdley KV.
    J Clin Gastroenterol; 2009 Jul 02; 43(6):569-73. PubMed ID: 19359997
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