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Journal Abstract Search

436 related items for PubMed ID: 12681966

  • 21. 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; 89(8):767-73. PubMed ID: 20107990
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  • 22. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
    Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.
    Ann Hematol; 2005 Mar; 84(3):146-9. PubMed ID: 15042317
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  • 23. Molecular diagnosis of hereditary hemochromatosis: application of a newly-developed reverse-hybridization assay in the South African population.
    Kotze MJ, de Villiers JN, Bouwens CS, Warnich L, Zaahl MG, van der Merwe S, Oberkanins C.
    Clin Genet; 2004 Apr; 65(4):317-21. PubMed ID: 15025725
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  • 24. HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors.
    Arya N, Chakrabrati S, Hegele RA, Adams PC.
    Blood Cells Mol Dis; 1999 Apr; 25(5-6):354-7. PubMed ID: 10660483
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  • 25. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH.
    Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565
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  • 26. 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 Feb; 18(7):685-9. PubMed ID: 12952143
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  • 27. Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation.
    Mattman A, Huntsman D, Lockitch G, Langlois S, Buskard N, Ralston D, Butterfield Y, Rodrigues P, Jones S, Porto G, Marra M, De Sousa M, Vatcher G.
    Blood; 2002 Aug 01; 100(3):1075-7. PubMed ID: 12130528
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  • 28. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P, Dalhoff K, Dissing J, Kramer I, Milman N, Pedersen P, Simonsen K, Tygstrup N, Nielsen FC.
    Scand J Clin Lab Invest; 2002 Aug 01; 62(7):527-35. PubMed ID: 12512743
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  • 35. Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestry.
    Salvioni A, Mariani R, Oberkanins C, Moritz A, Mauri V, Pelucchi S, Riva A, Arosio C, Cerutti P, Piperno A.
    Haematologica; 2003 Mar 01; 88(3):250-5. PubMed ID: 12651261
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  • 36. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ.
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr 01; 30(4):223-8. PubMed ID: 19731820
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  • 37. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.
    Phatak PD, Ryan DH, Cappuccio J, Oakes D, Braggins C, Provenzano K, Eberly S, Sham RL.
    Blood Cells Mol Dis; 2002 Apr 01; 29(1):41-7. PubMed ID: 12482402
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  • 40. A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis.
    Girelli D, Trombini P, Busti F, Campostrini N, Sandri M, Pelucchi S, Westerman M, Ganz T, Nemeth E, Piperno A, Camaschella C.
    Haematologica; 2011 Apr 01; 96(4):500-6. PubMed ID: 21173098
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