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Journal Abstract Search

436 related items for PubMed ID: 15986199

  • 1. 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; 84(10):650-5. PubMed ID: 15986199
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 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. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186
    [Abstract] [Full Text] [Related]

  • 6. 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 28; 84(12):802-6. PubMed ID: 15995871
    [Abstract] [Full Text] [Related]

  • 7. 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 28; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 8. 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 28; 69(4):295-301. PubMed ID: 10870847
    [Abstract] [Full Text] [Related]

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  • 10. 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 28; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 11. [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 28; 202(10):534-9. PubMed ID: 12361551
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. 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 15; 36(4):474-9. PubMed ID: 11943417
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 18(7):685-9. PubMed ID: 12952143
    [Abstract] [Full Text] [Related]

  • 15. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ.
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr 15; 30(4):223-8. PubMed ID: 19731820
    [Abstract] [Full Text] [Related]

  • 16. Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.
    Viprakasit V, Vathesathokit P, Chinchang W, Tachavanich K, Pung-Amritt P, Wimhurst VL, Yenchitsomanus PT, Merryweather-Clarke AT, Tanphaichitr VS.
    Eur J Haematol; 2004 Jul 15; 73(1):43-9. PubMed ID: 15182337
    [Abstract] [Full Text] [Related]

  • 17. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH.
    Circ Cardiovasc Genet; 2009 Feb 15; 2(1):34-7. PubMed ID: 20031565
    [Abstract] [Full Text] [Related]

  • 18. The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
    Martins R, Picanço I, Fonseca A, Ferreira L, Rodrigues O, Coelho M, Seixas T, Miranda A, Nunes B, Costa L, Romão L, Faustino P.
    J Hum Genet; 2004 Feb 15; 49(12):651-655. PubMed ID: 15538648
    [Abstract] [Full Text] [Related]

  • 19. Correlates of hepcidin and NTBI according to HFE status in patients referred to a liver centre.
    Ryan E, Ryan JD, Russell J, Coughlan B, Tjalsma H, Swinkels DW, Stewart S, Crowe JP.
    Acta Haematol; 2015 Feb 15; 133(2):155-61. PubMed ID: 25277871
    [Abstract] [Full Text] [Related]

  • 20. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
    Njajou OT, Houwing-Duistermaat JJ, Osborne RH, Vaessen N, Vergeer J, Heeringa J, Pols HA, Hofman A, van Duijn CM.
    Eur J Hum Genet; 2003 Mar 15; 11(3):225-31. PubMed ID: 12673276
    [Abstract] [Full Text] [Related]

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