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

767 related items for PubMed ID: 14571105

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

  • 22. HFE gene mutations in patients with altered iron metabolism in Argentina.
    Rossetti MV, Méndez M, Afonso S, Gerez E, Batlle A, Muñoz A, Parera V.
    Cell Mol Biol (Noisy-le-grand); 2009 Jul 01; 55(2):31-5. PubMed ID: 19656448
    [Abstract] [Full Text] [Related]

  • 23. Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience.
    De Gobbi M, D'Antico S, Castagno F, Testa D, Merlini R, Bondi A, Camaschella C.
    Haematologica; 2004 Oct 01; 89(10):1161-7. PubMed ID: 15477198
    [Abstract] [Full Text] [Related]

  • 24. 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 01; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 25. 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 01; 27(7):390-2. PubMed ID: 23862168
    [Abstract] [Full Text] [Related]

  • 26. [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 01; 128(5):600-4. PubMed ID: 11427792
    [Abstract] [Full Text] [Related]

  • 27. Natural history of HFE simple heterozygosity for C282Y and H63D: a prospective 12-year study.
    Zaloumis SG, Allen KJ, Bertalli NA, Turkovic L, Delatycki MB, Nicoll AJ, McLaren CE, English DR, Hopper JL, Giles GG, Anderson GJ, Olynyk JK, Powell LW, Gurrin LC, HealthIron Study Investigators.
    J Gastroenterol Hepatol; 2015 Apr 01; 30(4):719-25. PubMed ID: 25311314
    [Abstract] [Full Text] [Related]

  • 28. HFE mutations, hepatic iron, and fibrosis: ethnic-specific association of NASH with C282Y but not with fibrotic severity.
    Chitturi S, Weltman M, Farrell GC, McDonald D, Kench J, Liddle C, Samarasinghe D, Lin R, Abeygunasekera S, George J.
    Hepatology; 2002 Jul 01; 36(1):142-9. PubMed ID: 12085358
    [Abstract] [Full Text] [Related]

  • 29. 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 01; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 30. Iron absorption by heterozygous carriers of the HFE C282Y mutation associated with hemochromatosis.
    Hunt JR, Zeng H.
    Am J Clin Nutr; 2004 Oct 01; 80(4):924-31. PubMed ID: 15447900
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Frequencies of C282Y and H63D mutations and transferrin saturation indices in the Korean population.
    Choi SJ, Min WK, Chun S, Park H, Kim JW, Park CJ, Chi HS.
    Clin Chem Lab Med; 2002 Jul 01; 40(7):689-92. PubMed ID: 12241015
    [Abstract] [Full Text] [Related]

  • 36. HFE genotype in patients with hemochromatosis and other liver diseases.
    Bacon BR, Olynyk JK, Brunt EM, Britton RS, Wolff RK.
    Ann Intern Med; 1999 Jun 15; 130(12):953-62. PubMed ID: 10383365
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. 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]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V, Ryan E, O'Keane C, Crowe J.
    Blood Cells Mol Dis; 2000 Feb 15; 26(1):2-8. PubMed ID: 10772870
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 39.