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Journal Abstract Search

97 related items for PubMed ID: 17160266

  • 41. Spectrum and haplotypes of the HFE hemochromatosis gene in Iran: H63D in beta-thalassemia major and the first E277K homozygous.
    Karimi M, Yavarian M, Delbini P, Harteveld CL, Farjadian S, Fiorelli G, Giordano PC.
    Hematol J; 2004; 5(6):524-7. PubMed ID: 15570296
    [Abstract] [Full Text] [Related]

  • 42. Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C.
    Sumner K, Hubley L, Pont-Kingdon G, Mitchell S, Wayman T, Wilson A, Meadows C, Elenitoba-Johnson K, Pattison D, Dobrowolski S, Best H, Lyon E.
    Genet Test Mol Biomarkers; 2012 Jul; 16(7):656-60. PubMed ID: 22364140
    [Abstract] [Full Text] [Related]

  • 43. HFE gene mutations, hepatic iron content, and histological severity in hepatitis C virus-induced chronic hepatitis.
    Ladero JM, Ropero P, Ortega L, Taxonera C, González FA, López-Alonso G, Briceño O, Rodríguez-Agulló JL, González L, Villegas A, Díaz-Rubio M.
    Rev Esp Enferm Dig; 2003 Dec; 95(12):829-36. PubMed ID: 14972004
    [Abstract] [Full Text] [Related]

  • 44. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?
    Santos PC, Pereira AC, Cançado RD, Schettert IT, Sobreira TJ, Oliveira PS, Hirata RD, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2010 Dec 15; 45(4):302-7. PubMed ID: 20843714
    [Abstract] [Full Text] [Related]

  • 45. Association between hemochromatosis (HFE) gene mutation carrier status and the risk of colon cancer.
    Shaheen NJ, Silverman LM, Keku T, Lawrence LB, Rohlfs EM, Martin CF, Galanko J, Sandler RS.
    J Natl Cancer Inst; 2003 Jan 15; 95(2):154-9. PubMed ID: 12529348
    [Abstract] [Full Text] [Related]

  • 46. HFE based re-evaluation of heterozygous hemochromatosis.
    Moirand R, Guyader D, Mendler MH, Jouanolle AM, Le Gall JY, David V, Brissot P, Deugnier Y.
    Am J Med Genet; 2002 Sep 01; 111(4):356-61. PubMed ID: 12210292
    [Abstract] [Full Text] [Related]

  • 47. Simultaneous detection of HFE C282Y, H63D and S65C mutations associated with type 1 haemochromatosis using a multiplex luminex bead assay.
    Cardoso SP, Patel R, Brown C, Navarrete C.
    Tissue Antigens; 2011 Sep 01; 78(3):171-7. PubMed ID: 21736562
    [Abstract] [Full Text] [Related]

  • 48. [Polymorphism of the HFE gene associated with hereditary hemochromatosis in populations of Russia].
    Mikhaĭlova SV, Kobzev VF, Kulikov IV, Romashchenko AG, Khasnulin VI, Voevoda MI.
    Genetika; 2003 Jul 01; 39(7):988-95. PubMed ID: 12942784
    [Abstract] [Full Text] [Related]

  • 49. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
    Njajou OT, Houwing-Duistermaat JJ, Osborne RH, Vaessen N, Vergeer J, Heeringa J, Pols HA, Hofman A, van Duijn CM.
    Eur J Hum Genet; 2003 Mar 01; 11(3):225-31. PubMed ID: 12673276
    [Abstract] [Full Text] [Related]

  • 50. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
    De Marco F, Liguori R, Giardina MG, D'Armiento M, Angelucci E, Lucariello A, Morante R, Cimino L, Galeota-Lanza A, Tarantino G, Ascione A, Budillon G, Vecchione R, Martinelli R, Matarazzo M, De Simone V.
    Clin Chem Lab Med; 2004 Jan 01; 42(1):17-24. PubMed ID: 15061375
    [Abstract] [Full Text] [Related]

  • 51. DNA testing for haemochromatosis: diagnostic, predictive and screening implications.
    Trent RJ, Le H, Yu B, Young G, Bowden DK.
    Pathology; 2000 Nov 01; 32(4):274-9. PubMed ID: 11186424
    [Abstract] [Full Text] [Related]

  • 52. [Mutations in the HFE gene in patients with rheumatic diseases].
    Půtová I, Cimburová M, Jarosová K, Vencovský J, Horák J.
    Cas Lek Cesk; 2005 Nov 01; 144(6):391-7; discussion 397-8. PubMed ID: 16047841
    [Abstract] [Full Text] [Related]

  • 53. Comment on: Hemochromatosis (HFE) gene mutations (H63D and C282Y) and iron overload in beta-thalassemia major.
    Yasri S, Wiwanitkit V.
    Saudi Med J; 2019 Nov 01; 40(11):1178. PubMed ID: 31707418
    [Abstract] [Full Text] [Related]

  • 54. Hereditary hemochromatosis in north-eastern Romania.
    Voicu PM, Cojocariu C, Petrescu-Dănilă E, Stanciu C, Covic M, Rusu M, Trifan A.
    Rev Med Chir Soc Med Nat Iasi; 2010 Nov 01; 114(4):982-7. PubMed ID: 21495455
    [Abstract] [Full Text] [Related]

  • 55. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.
    De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C.
    Haematologica; 2003 Apr 01; 88(4):396-401. PubMed ID: 12681966
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  • 58. HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions.
    Sharma V, Panigrahi I, Dutta P, Tyagi S, Choudhry VP, Saxena R.
    Indian J Pathol Microbiol; 2007 Jan 01; 50(1):82-5. PubMed ID: 17474269
    [Abstract] [Full Text] [Related]

  • 59. 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]

  • 60. 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 Jul 01; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

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