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284 related items for PubMed ID: 20594259

  • 1. 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; 25(7):1295-8. PubMed ID: 20594259
    [Abstract] [Full Text] [Related]

  • 2. [Role of the hemochromatosis gene in prophyria cutanea tarda. Prospective study of 56 cases].
    Skowron F, Bérard F, Grézard P, Wolf F, Morel Y, Perrot H.
    Ann Dermatol Venereol; 2001 May; 128(5):600-4. PubMed ID: 11427792
    [Abstract] [Full Text] [Related]

  • 3. C282Y and H63D mutation of the hemochromatosis gene in German porphyria cutanea tarda patients.
    Tannapfel A, Stölzel U, Köstler E, Melz S, Richter M, Keim V, Schuppan D, Wittekind C.
    Virchows Arch; 2001 Jul; 439(1):1-5. PubMed ID: 11499833
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis.
    Canavese C, Bergamo D, Barbieri S, Timbaldi M, Thea A, Martina G, Damiani D, Fenoglio R, Donati-Marella B, Priolo G.
    Clin Nephrol; 2002 Dec 28; 58(6):438-44. PubMed ID: 12508966
    [Abstract] [Full Text] [Related]

  • 6. The prevalence of HFE C282Y gene mutation is increased in Spanish patients with porphyria cutanea tarda without hepatitis C virus infection.
    Toll A, Celis R, Ozalla MD, Bruguera M, Herrero C, Ercilla MG.
    J Eur Acad Dermatol Venereol; 2006 Nov 28; 20(10):1201-6. PubMed ID: 17062032
    [Abstract] [Full Text] [Related]

  • 7. 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 Nov 28; 18(7):685-9. PubMed ID: 12952143
    [Abstract] [Full Text] [Related]

  • 8. 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 28; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 9. Screening for iron overload in the Turkish population.
    Barut G, Balci H, Bozdayi M, Hatemi I, Ozcelik D, Senturk H.
    Dig Dis; 2003 Jun 28; 21(3):279-85. PubMed ID: 14571105
    [Abstract] [Full Text] [Related]

  • 10. Initial screening transferrin saturation values, serum ferritin concentrations, and HFE genotypes in whites and blacks in the Hemochromatosis and Iron Overload Screening Study.
    Barton JC, Acton RT, Dawkins FW, Adams PC, Lovato L, Leiendecker-Foster C, McLaren CE, Reboussin DM, Speechley MR, Gordeuk VR, McLaren GD, Sholinsky P, Harris EL.
    Genet Test; 2005 Jun 28; 9(3):231-41. PubMed ID: 16225403
    [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. 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 28; 89(8):767-73. PubMed ID: 20107990
    [Abstract] [Full Text] [Related]

  • 13. Population screening for hemochromatosis: a study in 5370 Spanish blood donors.
    Sánchez M, Villa M, Ingelmo M, Sanz C, Bruguera M, Ascaso C, Oliva R.
    J Hepatol; 2003 Jun 28; 38(6):745-50. PubMed ID: 12763366
    [Abstract] [Full Text] [Related]

  • 14. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M, de Salamanca RE, Morales P, Martínez-Laso J, Fontanellas A, Castro MJ, Rojo R, Moscoso J, Zamora J, Serrano-Vela JI, Arnaiz-Villena A.
    J Gastroenterol Hepatol; 2005 Mar 28; 20(3):456-62. PubMed ID: 15740492
    [Abstract] [Full Text] [Related]

  • 15. HFE mutations in Caucasian participants of the Hemochromatosis and Iron Overload Screening study with serum ferritin level <1000 µg/L.
    Adams PC, McLaren CE, Speechley M, McLaren GD, Barton JC, Eckfeldt JH.
    Can J Gastroenterol; 2013 Jul 28; 27(7):390-2. PubMed ID: 23862168
    [Abstract] [Full Text] [Related]

  • 16. Differences in hepatic phenotype between hemochromatosis patients with HFE C282Y homozygosity and other HFE genotypes.
    Cheng R, Barton JC, Morrison ED, Phatak PD, Krawitt EL, Gordon SC, Kowdley KV.
    J Clin Gastroenterol; 2009 Jul 28; 43(6):569-73. PubMed ID: 19359997
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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]

  • 19. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug 28; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 20. 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 Aug 28; 4(6):436-40. PubMed ID: 14671617
    [Abstract] [Full Text] [Related]

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