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

713 related items for PubMed ID: 15871018

  • 1. 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]

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

  • 3. 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; 70(3):252-5. PubMed ID: 17661915
    [Abstract] [Full Text] [Related]

  • 4. 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; 35(3):329-35. PubMed ID: 11887210
    [Abstract] [Full Text] [Related]

  • 5. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Mar; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.
    Genet Mol Res; 2005 Mar 31; 4(1):31-8. PubMed ID: 15841433
    [Abstract] [Full Text] [Related]

  • 8. 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 31; 84(12):802-6. PubMed ID: 15995871
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. A 6-year survey of HFE gene test for hemochromatosis diagnosis.
    Mura C, Raguénes O, Scotet V, Jacolot S, Mercier AY, Férec C.
    Genet Med; 2005 Jan 23; 7(1):68-73. PubMed ID: 15654232
    [Abstract] [Full Text] [Related]

  • 11. 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 23; 70(4):294-300. PubMed ID: 17767550
    [Abstract] [Full Text] [Related]

  • 12. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.
    Scand J Gastroenterol; 2001 Nov 23; 36(11):1211-6. PubMed ID: 11686223
    [Abstract] [Full Text] [Related]

  • 13. 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 Nov 23; 49(12):651-655. PubMed ID: 15538648
    [Abstract] [Full Text] [Related]

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

  • 15. Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.
    Tomatsu S, Orii KO, Fleming RE, Holden CC, Waheed A, Britton RS, Gutierrez MA, Velez-Castrillon S, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 2003 Dec 23; 100(26):15788-93. PubMed ID: 14673107
    [Abstract] [Full Text] [Related]

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

  • 17. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 23; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

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

  • 19. Frequency of HFE mutations among Turkish blood donors according to transferrin saturation: genotype screening for hereditary hemochromatosis among voluntary blood donors in Turkey.
    Simsek H, Sumer H, Yilmaz E, Balaban YH, Ozcebe O, Hascelik G, Buyukask Y, Tatar G.
    J Clin Gastroenterol; 2004 Sep 23; 38(8):671-5. PubMed ID: 15319650
    [Abstract] [Full Text] [Related]

  • 20. Primary osteoarthritis in the ankle joint is associated with finger metacarpophalangeal osteoarthritis and the H63D mutation in the HFE gene: evidence for a hemochromatosis-like polyarticular osteoarthritis phenotype.
    Carroll GJ.
    J Clin Rheumatol; 2006 Jun 23; 12(3):109-13. PubMed ID: 16755236
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 36.