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Journal Abstract Search

235 related items for PubMed ID: 23102134

  • 1. [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; 151(9):428-31. PubMed ID: 23102134
    [Abstract] [Full Text] [Related]

  • 2. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L, Juzenas S, Sventoraityte J, Cedaviciute R, Vitkauskiene A, Kalibatas V, Kondrackiene J, Kupcinskas L.
    Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
    [Abstract] [Full Text] [Related]

  • 3. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
    [Abstract] [Full Text] [Related]

  • 4. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
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  • 5. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun 23; 21(2):177-80. PubMed ID: 22720307
    [Abstract] [Full Text] [Related]

  • 6. 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 Jun 23; 8(4):407-10. PubMed ID: 15684872
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  • 8. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C, Murga MJ, Martínez-Castro P.
    Genet Test; 2004 Jun 23; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 9. Analysis of the HFE gene (C282Y, H63D and S65C) mutations in a general Chinese Han population.
    Lin A, Yan WH, Xu HH, Zhu M, Zhou MY.
    Tissue Antigens; 2007 Sep 23; 70(3):252-5. PubMed ID: 17661915
    [Abstract] [Full Text] [Related]

  • 10. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D.
    Med Sci Monit; 2011 Oct 23; 17(10):CR552-6. PubMed ID: 21959608
    [Abstract] [Full Text] [Related]

  • 11. 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 23; 84(3):146-9. PubMed ID: 15042317
    [Abstract] [Full Text] [Related]

  • 12. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
    Spínola C, Brehm A, Spínola H.
    Ann Hematol; 2011 Jan 23; 90(1):29-32. PubMed ID: 20714725
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  • 14. Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
    Hannuksela J, Leppilampi M, Peuhkurinen K, Kärkkäinen S, Saastamoinen E, Heliö T, Kaartinen M, Nieminen MS, Nieminen P, Parkkila S.
    Eur J Heart Fail; 2005 Jan 23; 7(1):103-8. PubMed ID: 15642540
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 78(3):171-7. PubMed ID: 21736562
    [Abstract] [Full Text] [Related]

  • 16. Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same region.
    Alkhateeb A, Uzrail A, Bodoor K.
    Dis Markers; 2009 Sep 23; 27(1):17-22. PubMed ID: 19822954
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  • 18. 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
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