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Journal Abstract Search


164 related items for PubMed ID: 24395214

  • 1. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD, Freire JM, Cunha Fernandes AL, Moura de Oliveira TM, Leão ND, Gil EA, de Vasconcelos RC, Azevedo JP, de Farias Sales VS, de Araújo Moura Lemos TM, Leão MD, do Nascimento FF, Maciel JF, de Freitas RV, de Souza Paiva A, Cavalcanti GB.
    J Clin Lab Anal; 2014 May; 28(3):178-85. PubMed ID: 24395214
    [Abstract] [Full Text] [Related]

  • 2. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C, Murga MJ, Martínez-Castro P.
    Genet Test; 2004 May; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 3. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
    [Abstract] [Full Text] [Related]

  • 4. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun 23; 21(2):177-80. PubMed ID: 22720307
    [Abstract] [Full Text] [Related]

  • 5. 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 Jun 23; 18(7):685-9. PubMed ID: 12952143
    [Abstract] [Full Text] [Related]

  • 6. 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 23; 35(3):329-35. PubMed ID: 11887210
    [Abstract] [Full Text] [Related]

  • 7. S65C and other mutations in the haemochromatosis gene in the Czech population.
    Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J.
    Folia Biol (Praha); 2005 Mar 23; 51(6):172-6. PubMed ID: 16419611
    [Abstract] [Full Text] [Related]

  • 8. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L, Juzenas S, Sventoraityte J, Cedaviciute R, Vitkauskiene A, Kalibatas V, Kondrackiene J, Kupcinskas L.
    Ann Hematol; 2012 Apr 23; 91(4):491-5. PubMed ID: 21947086
    [Abstract] [Full Text] [Related]

  • 9. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.
    Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.
    Tissue Antigens; 2007 Sep 23; 70(3):252-5. PubMed ID: 17661915
    [Abstract] [Full Text] [Related]

  • 10. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
    Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.
    Ann Hematol; 2005 Mar 23; 84(3):146-9. PubMed ID: 15042317
    [Abstract] [Full Text] [Related]

  • 11. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
    Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M.
    Genet Test; 2004 Mar 23; 8(4):407-10. PubMed ID: 15684872
    [Abstract] [Full Text] [Related]

  • 12. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.
    Aranda N, Viteri FE, Montserrat C, Arija V.
    Ann Hematol; 2010 Aug 23; 89(8):767-73. PubMed ID: 20107990
    [Abstract] [Full Text] [Related]

  • 13. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D.
    Med Sci Monit; 2011 Oct 23; 17(10):CR552-6. PubMed ID: 21959608
    [Abstract] [Full Text] [Related]

  • 14. [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 23; 202(10):534-9. PubMed ID: 12361551
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 25(3-4):147-55. PubMed ID: 10575540
    [Abstract] [Full Text] [Related]

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

  • 17. 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]

  • 18. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb 15; 84(2):103-5. PubMed ID: 15517265
    [Abstract] [Full Text] [Related]

  • 19. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
    Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC.
    Clinics (Sao Paulo); 2009 Feb 15; 64(9):837-41. PubMed ID: 19759876
    [Abstract] [Full Text] [Related]

  • 20. 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 Feb 15; 62(7):527-35. PubMed ID: 12512743
    [Abstract] [Full Text] [Related]


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