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544 related items for PubMed ID: 17661915

  • 21. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
    Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.
    Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018
    [Abstract] [Full Text] [Related]

  • 22. HFE gene mutations in patients with altered iron metabolism in Argentina.
    Rossetti MV, Méndez M, Afonso S, Gerez E, Batlle A, Muñoz A, Parera V.
    Cell Mol Biol (Noisy-le-grand); 2009 Jul 01; 55(2):31-5. PubMed ID: 19656448
    [Abstract] [Full Text] [Related]

  • 23. Hereditary hemochromatosis: the clinical significance of the S65C mutation.
    Asberg A, Thorstensen K, Hveem K, Bjerve KS.
    Genet Test; 2002 Jul 01; 6(1):59-62. PubMed ID: 12180078
    [Abstract] [Full Text] [Related]

  • 24. 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 Jul 01; 62(7):527-35. PubMed ID: 12512743
    [Abstract] [Full Text] [Related]

  • 25. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA.
    Rev Clin Esp; 2002 Oct 01; 202(10):534-9. PubMed ID: 12361551
    [Abstract] [Full Text] [Related]

  • 26. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999 Oct 01; 25(3-4):147-55. PubMed ID: 10575540
    [Abstract] [Full Text] [Related]

  • 27. Frequencies of the haemochromatosis gene (HFE) variants C282Y, H63D and S65C in 6,020 ethnic Danish men.
    Pedersen P, Melsen GV, Milman N.
    Ann Hematol; 2008 Sep 01; 87(9):735-40. PubMed ID: 18542962
    [Abstract] [Full Text] [Related]

  • 28. HFE gene mutations analysis in Basque hereditary haemochromatosis patients and controls.
    de Juan D, Reta A, Castiella A, Pozueta J, Prada A, Cuadrado E.
    Eur J Hum Genet; 2001 Dec 01; 9(12):961-4. PubMed ID: 11840200
    [Abstract] [Full Text] [Related]

  • 29. 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 01; 35(3):329-35. PubMed ID: 11887210
    [Abstract] [Full Text] [Related]

  • 30. 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
    [Abstract] [Full Text] [Related]

  • 31. Frequency of the HFE gene mutations in five Italian populations.
    Candore G, Mantovani V, Balistreri CR, Lio D, Colonna-Romano G, Cerreta V, Carru C, Deiana L, Pes G, Menardi G, Perotti L, Miotti V, Bevilacqua E, Amoroso A, Caruso C.
    Blood Cells Mol Dis; 2002 Mar 02; 29(3):267-73. PubMed ID: 12547216
    [Abstract] [Full Text] [Related]

  • 32. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.
    Floreani A, Rosa Rizzotto E, Basso D, Navaglia F, Zaninotto M, Petridis I, DI Andrea O, Testa R, Marra M, Baldo V, Chiaramonte M.
    Aliment Pharmacol Ther; 2007 Aug 15; 26(4):577-86. PubMed ID: 17661761
    [Abstract] [Full Text] [Related]

  • 33. Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay.
    Cardoso SP, Patel R, Brown C, Navarrete C.
    Tissue Antigens; 2011 Sep 15; 78(3):171-7. PubMed ID: 21736562
    [Abstract] [Full Text] [Related]

  • 34. Prevalence of hemochromatosis gene (HFE) mutations in Greece.
    Papazoglou D, Exiara T, Speletas M, Panagopoulos I, Maltezos E.
    Acta Haematol; 2003 Sep 15; 109(3):137-40. PubMed ID: 12714823
    [Abstract] [Full Text] [Related]

  • 35. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M, Putova I, Provaznikova H, Horak J.
    Genet Epidemiol; 2002 Oct 15; 23(3):260-3. PubMed ID: 12384978
    [Abstract] [Full Text] [Related]

  • 36. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2011 Apr 15; 46(4):302-7. PubMed ID: 21411349
    [Abstract] [Full Text] [Related]

  • 37. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
    Sassi R, Hmida S, Kaabi H, Hajjej A, Abid A, Abdelkefi S, Yacoub S, Maamar M, Mojaat N, Ben Hamed L, Bellali H, Dridi A, Jridi A, Midouni B, Boukef MK.
    Ann Genet; 2004 Apr 15; 47(4):325-30. PubMed ID: 15581829
    [Abstract] [Full Text] [Related]

  • 38. Analysis of haemochromatosis gene mutations in a population from the Mediterranean Basin.
    Campo S, Restuccia T, Villari D, Raffa G, Cucinotta D, Squadrito G, Pollicino T, Raimondo G.
    Liver; 2001 Aug 15; 21(4):233-6. PubMed ID: 11454185
    [Abstract] [Full Text] [Related]

  • 39. Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism.
    Gómez-Llorente C, Miranda-León MT, Blanco S, Gandia-Pla S, Gómez-Capilla JA, Fárez-Vidal ME.
    Ann Hematol; 2005 Oct 15; 84(10):650-5. PubMed ID: 15986199
    [Abstract] [Full Text] [Related]

  • 40. Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina.
    Terzić R, Sehić A, Teran N, Terzić I, Peterlin B.
    Coll Antropol; 2006 Sep 15; 30(3):555-7. PubMed ID: 17058523
    [Abstract] [Full Text] [Related]

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