These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

446 related items for PubMed ID: 20107990

  • 1. 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; 89(8):767-73. PubMed ID: 20107990
    [Abstract] [Full Text] [Related]

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

  • 3. [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; 202(10):534-9. PubMed ID: 12361551
    [Abstract] [Full Text] [Related]

  • 4. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
    Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P.
    Gut; 2002 Nov; 51(5):723-30. PubMed ID: 12377814
    [Abstract] [Full Text] [Related]

  • 5. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.
    Wallace DF, Walker AP, Pietrangelo A, Clare M, Bomford AB, Dixon JL, Powell LW, Subramaniam VN, Dooley JS.
    J Hepatol; 2002 Apr 23; 36(4):474-9. PubMed ID: 11943417
    [Abstract] [Full Text] [Related]

  • 8. 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 Apr 23; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. 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 23; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 11. 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 23; 84(10):650-5. PubMed ID: 15986199
    [Abstract] [Full Text] [Related]

  • 12. Screening for iron overload in the Turkish population.
    Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H.
    Dig Dis; 2003 Oct 23; 21(3):279-85. PubMed ID: 14571105
    [Abstract] [Full Text] [Related]

  • 13. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
    Vizzi E, Loureiro CL, Gerder M, de las Nieves Garcia-Casal M, Rodríguez-Larralde A, Gerace L, Ludert JE, Liprandi F, Pujol FH.
    Ann Hematol; 2005 Nov 23; 84(12):802-6. PubMed ID: 15995871
    [Abstract] [Full Text] [Related]

  • 14. 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 Nov 23; 62(7):527-35. PubMed ID: 12512743
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. 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 23; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 17. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.
    Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.
    Hematol J; 2003 Nov 23; 4(6):436-40. PubMed ID: 14671617
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct 02; 70(4):294-300. PubMed ID: 17767550
    [Abstract] [Full Text] [Related]

  • 20. Hereditary hemochromatosis: the clinical significance of the S65C mutation.
    Asberg A, Thorstensen K, Hveem K, Bjerve KS.
    Genet Test; 2002 Oct 02; 6(1):59-62. PubMed ID: 12180078
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 23.