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Journal Abstract Search

767 related items for PubMed ID: 14571105

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

  • 2. 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; 4(6):436-40. PubMed ID: 14671617
    [Abstract] [Full Text] [Related]

  • 3. A population-based study of the clinical expression of the hemochromatosis gene.
    Olynyk JK, Cullen DJ, Aquilia S, Rossi E, Summerville L, Powell LW.
    N Engl J Med; 1999 Sep 02; 341(10):718-24. PubMed ID: 10471457
    [Abstract] [Full Text] [Related]

  • 4. 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 02; 89(8):767-73. PubMed ID: 20107990
    [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. 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 28; 18(7):685-9. PubMed ID: 12952143
    [Abstract] [Full Text] [Related]

  • 7. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.
    Isr Med Assoc J; 2004 Jan 28; 6(1):30-3. PubMed ID: 14740507
    [Abstract] [Full Text] [Related]

  • 8. 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 28; 38(8):671-5. PubMed ID: 15319650
    [Abstract] [Full Text] [Related]

  • 9. 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 28; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 10. Significance of H63D homozygosity in a Basque population with hemochromatosis.
    Castiella A, Zapata E, de Juan MD, Otazua P, Fernandez J, Zubiaurre L, Arriola JA, Gipuzkoa Hemochromatosis Group.
    J Gastroenterol Hepatol; 2010 Jul 28; 25(7):1295-8. PubMed ID: 20594259
    [Abstract] [Full Text] [Related]

  • 11. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
    Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK.
    Gastroenterology; 2002 Mar 28; 122(3):646-51. PubMed ID: 11874997
    [Abstract] [Full Text] [Related]

  • 12. 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 28; 70(4):294-300. PubMed ID: 17767550
    [Abstract] [Full Text] [Related]

  • 13. The prevalence of primary hereditary hemochromatosis in central Anatolia.
    Karaca H, Güven K, Önal M, Gürsoy Ş, Başkol M, Özkul Y.
    Turk J Gastroenterol; 2013 Oct 28; 24(1):43-50. PubMed ID: 23794343
    [Abstract] [Full Text] [Related]

  • 14. Testing for haemochromatosis in a liver clinic population: relationship between ethnic origin, HFE gene mutations, liver histology and serum iron markers.
    Moodie SJ, Ang L, Stenner JM, Finlayson C, Khotari A, Levin GE, Maxwell JD.
    Eur J Gastroenterol Hepatol; 2002 Mar 28; 14(3):223-9. PubMed ID: 11953685
    [Abstract] [Full Text] [Related]

  • 15. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis.
    Walsh A, Dixon JL, Ramm GA, Hewett DG, Lincoln DJ, Anderson GJ, Subramaniam VN, Dodemaide J, Cavanaugh JA, Bassett ML, Powell LW.
    Clin Gastroenterol Hepatol; 2006 Nov 28; 4(11):1403-10. PubMed ID: 16979952
    [Abstract] [Full Text] [Related]

  • 16. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.
    Cassanelli S, Pignatti E, Montosi G, Garuti C, Mariano M, Campioli D, Carbonieri A, Baldini E, Pietrangelo A.
    J Hepatol; 2001 Apr 28; 34(4):523-8. PubMed ID: 11394651
    [Abstract] [Full Text] [Related]

  • 17. Screening for C282Y homozygosity in a Norwegian population (HUNT2): The sensitivity and specificity of transferrin saturation.
    Thorstensen K, Kvitland MA, Irgens WØ, Hveem K, Asberg A.
    Scand J Clin Lab Invest; 2010 Apr 28; 70(2):92-7. PubMed ID: 20073670
    [Abstract] [Full Text] [Related]

  • 18. Hereditary hemochromatosis: population screening based on phenotype in Brazilian blood donors.
    Barbosa KV, de Souza AF, Chebli JM, Proietti FA, Meirelles RS, de Souza JL.
    J Clin Gastroenterol; 2005 Apr 28; 39(5):430-4. PubMed ID: 15815212
    [Abstract] [Full Text] [Related]

  • 19. 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]

  • 20. 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 31; 2(1):34-7. PubMed ID: 20031565
    [Abstract] [Full Text] [Related]

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