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Journal Abstract Search

807 related items for PubMed ID: 9510559

  • 1. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr; 47(5):404-10. PubMed ID: 9510559
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  • 2. Co-selection of the H63D mutation and the HLA-A29 allele: a new paradigm of linkage disequilibrium?
    Cardoso CS, Alves H, Mascarenhas M, Gonçalves R, Oliveira P, Rodrigues P, Cruz E, de Sousa M, Porto G.
    Immunogenetics; 2002 Mar; 53(12):1002-8. PubMed ID: 11904676
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  • 4. HLA haplotypes associated with hemochromatosis mutations in the Spanish population.
    Pacho A, Mancebo E, del Rey MJ, Castro MJ, Oliver D, García-Berciano M, González L, Morales P.
    BMC Med Genet; 2004 Oct 21; 5():25. PubMed ID: 15498100
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  • 5. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL, Palácios SA, Couto CA, Cançado EL, Carrilho FJ, Laudanna AA, Kalil J, Gayotto LC, Goldberg AC.
    Braz J Med Biol Res; 2002 Mar 21; 35(3):329-35. PubMed ID: 11887210
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  • 6. 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 21; 69(4):295-301. PubMed ID: 10870847
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  • 8. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC, Wiener HW, Acton RT, Go RC.
    Blood Cells Mol Dis; 2005 Apr 21; 34(1):38-47. PubMed ID: 15607698
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  • 9. Linkage disequilibrium between S65C HFE mutation and HLA A29-B44 haplotype in Terceira Island, Azores.
    Couto AR, Peixoto MJ, Garrett F, Laranjeira F, Cipriano T, Armas JB.
    Hum Immunol; 2003 Jun 21; 64(6):625-8. PubMed ID: 12770794
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  • 10. Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.
    Cançado RD, Guglielmi AC, Vergueiro CS, Rolim EG, Figueiredo MS, Chiattone CS.
    Sao Paulo Med J; 2006 Mar 02; 124(2):55-60. PubMed ID: 16878186
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  • 11. 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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  • 12. Phenotypic expression of HFE mutations: a French study of 1110 unrelated iron-overloaded patients and relatives.
    Moirand R, Jouanolle AM, Brissot P, Le Gall JY, David V, Deugnier Y.
    Gastroenterology; 1999 Feb 02; 116(2):372-7. PubMed ID: 9922318
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  • 13. 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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  • 14. 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 02; 23(2):314-20. PubMed ID: 9410475
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  • 18. 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 02; 30(4):588-93. PubMed ID: 10207799
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  • 19. HFE gene mutations an Apulian population: allele frequencies.
    Pietrapertosa A, Vitucci A, Campanale D, Palma A, Renni R, Delios G, Tannoia N.
    Eur J Epidemiol; 2003 Apr 02; 18(7):685-9. PubMed ID: 12952143
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  • 20. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
    Cruz E, Vieira J, Almeida S, Lacerda R, Gartner A, Cardoso CS, Alves H, Porto G.
    BMC Med Genet; 2006 Mar 01; 7():16. PubMed ID: 16509978
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