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Journal Abstract Search

179 related items for PubMed ID: 20084012

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

  • 42. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
    Drastíková M, Beránek M, Hegerová J, Putzová D.
    Cas Lek Cesk; 2012 Nov; 151(9):428-31. PubMed ID: 23102134
    [Abstract] [Full Text] [Related]

  • 43. Global prevalence of putative haemochromatosis mutations.
    Merryweather-Clarke AT, Pointon JJ, Shearman JD, Robson KJ.
    J Med Genet; 1997 Apr; 34(4):275-8. PubMed ID: 9138148
    [Abstract] [Full Text] [Related]

  • 44. 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; 30(4):719-25. PubMed ID: 25311314
    [Abstract] [Full Text] [Related]

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

  • 46. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in a cohort of 1,000 neonates in Madrid (Spain).
    Ropero P, Briceño O, Mateo M, Polo M, Mora A, González FA, Villegas A.
    Ann Hematol; 2006 May; 85(5):323-6. PubMed ID: 16520984
    [Abstract] [Full Text] [Related]

  • 47. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain.
    Altes A, Ruiz A, Barceló MJ, Remacha AF, Puig T, Maya AJ, Castell C, Amate JM, Saz Z, Baiget M.
    Genet Test; 2004 May; 8(4):407-10. PubMed ID: 15684872
    [Abstract] [Full Text] [Related]

  • 48. 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]

  • 49. Prevalence and clinical significance of HFE gene mutations in patients with iron overload.
    Brandhagen DJ, Fairbanks VF, Baldus WP, Smith CI, Kruckeberg KE, Schaid DJ, Thibodeau SN.
    Am J Gastroenterol; 2000 Oct; 95(10):2910-4. PubMed ID: 11051367
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  • 51. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999 Oct; 25(3-4):147-55. PubMed ID: 10575540
    [Abstract] [Full Text] [Related]

  • 52. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote.
    Wallace DF, Dooley JS, Walker AP.
    Gastroenterology; 1999 Jun; 116(6):1409-12. PubMed ID: 10348824
    [Abstract] [Full Text] [Related]

  • 53. 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]

  • 54. 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; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 55. [Analysis of the hemochromatosis gene (HFE) mutations, C282Y and H63D, in the populations of Central Asia].
    Khusainova RI, Khusnutdinova NN, Khusnutdinova EK.
    Genetika; 2006 Mar; 42(3):421-6. PubMed ID: 16649670
    [Abstract] [Full Text] [Related]

  • 56. Differential HFE allele expression in hemochromatosis heterozygotes.
    Rosmorduc O, Poupon R, Nion I, Wendum D, Feder J, Béréziat G, Hermelin B.
    Gastroenterology; 2000 Oct; 119(4):1075-86. PubMed ID: 11040194
    [Abstract] [Full Text] [Related]

  • 57. HFE genotyping demonstrates a significant incidence of hemochromatosis in undifferentiated arthritis.
    Cauza E, Hanusch-Enserer U, Etemad M, Köller M, Kostner K, Georg P, Dunky A, Ferenci P.
    Clin Exp Rheumatol; 2005 Oct; 23(1):7-12. PubMed ID: 15789881
    [Abstract] [Full Text] [Related]

  • 58. 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; 34(4):523-8. PubMed ID: 11394651
    [Abstract] [Full Text] [Related]

  • 59. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
    Brissot P, Moirand R, Jouanolle AM, Guyader D, Le Gall JY, Deugnier Y, David V.
    J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
    [Abstract] [Full Text] [Related]

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