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Journal Abstract Search

161 related items for PubMed ID: 27561698

  • 41. Serum ferritin and transferrin saturation levels in β⁰ and β(+) thalassemia patients.
    Estevão IF, Peitl Junior P, Bonini-Domingos CR.
    Genet Mol Res; 2011 Apr 12; 10(2):632-9. PubMed ID: 21491373
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  • 42. Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population.
    Sassi R, Hmida S, Kaabi H, Hajjej A, Abid A, Abdelkefi S, Yacoub S, Maamar M, Mojaat N, Ben Hamed L, Bellali H, Dridi A, Jridi A, Midouni B, Boukef MK.
    Ann Genet; 2004 Apr 12; 47(4):325-30. PubMed ID: 15581829
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  • 43. 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
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  • 44. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City.
    Baptista-González HA, Rosenfeld-Mann F, Trueba-Gómez R, Bermejo-Martínez L, Méndez-Sánchez N.
    Ann Hepatol; 2007 Jun 15; 6(1):55-60. PubMed ID: 17297430
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  • 48. 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 15; 27(7):390-2. PubMed ID: 23862168
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  • 49. Iron Overload in an HFE Heterozygous Carrier: A Case Report and Literature Review.
    Turbiville D, Du X, Yo J, Jana BR, Dong J.
    Lab Med; 2019 Apr 08; 50(2):212-217. PubMed ID: 30339210
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  • 51. Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients.
    Perícole FV, Alves MA, Saad ST, Costa FF.
    Braz J Med Biol Res; 2005 Sep 08; 38(9):1321-4. PubMed ID: 16138214
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  • 53. 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
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  • 54. 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 Apr 28; 9(3):231-41. PubMed ID: 16225403
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  • 55. Distribution of C282Y and H63D mutations in the HFE gene in healthy Asian Indians and patients with thalassaemia major.
    Kaur G, Rapthap CC, Xavier M, Saxena R, Choudhary VP, Reuben SK, Mehra NK.
    Natl Med J India; 2003 Apr 28; 16(6):309-10. PubMed ID: 14765621
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  • 57. Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry.
    Beutler E, Felitti V, Gelbart T, Waalen J.
    Br J Haematol; 2003 Mar 28; 120(5):887-93. PubMed ID: 12614226
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