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Journal Abstract Search

102 related items for PubMed ID: 12737937

  • 21.
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  • 22. 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
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  • 23. Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis.
    Bittencourt PL, Palácios SA, Couto CA, Cançado EL, Carrilho FJ, Laudanna AA, Kalil J, Gayotto LC, Goldberg AC.
    Braz J Med Biol Res; 2002 Mar; 35(3):329-35. PubMed ID: 11887210
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  • 26. A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygote.
    Barton JC, West C, Lee PL, Beutler E.
    Clin Genet; 2004 Sep; 66(3):214-6. PubMed ID: 15324319
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  • 27. 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; 70(3):252-5. PubMed ID: 17661915
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  • 28. Mutation analysis of the HFE gene in German hemochromatosis patients and controls using automated SSCP-based capillary electrophoresis and a new PCR-ELISA technique.
    Hellerbrand C, Bosserhoff AK, Seegers S, Lingner G, Wrede C, Lock G, Schölmerich J, Büttner R.
    Scand J Gastroenterol; 2001 Nov; 36(11):1211-6. PubMed ID: 11686223
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  • 29. 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; 21(2):177-80. PubMed ID: 22720307
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  • 30. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
    Barton JC, Lafreniere SA, Leiendecker-Foster C, Li H, Acton RT, Press RD, Eckfeldt JH.
    Am J Hematol; 2009 Nov; 84(11):710-4. PubMed ID: 19787796
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  • 31. Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey.
    Yönal O, Hatirnaz O, Akyüz F, Köroğlu G, Ozbek U, Cefle K, Mungan Z.
    Turk J Gastroenterol; 2007 Mar; 18(1):53-7. PubMed ID: 17450498
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  • 32. 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; 7(1):103-8. PubMed ID: 15642540
    [Abstract] [Full Text] [Related]

  • 33. 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
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  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct 01; 70(4):294-300. PubMed ID: 17767550
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  • 36. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.
    Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.
    Hematol J; 2003 Oct 01; 4(6):436-40. PubMed ID: 14671617
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  • 37. 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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  • 38. Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism.
    Gómez-Llorente C, Miranda-León MT, Blanco S, Gandia-Pla S, Gómez-Capilla JA, Fárez-Vidal ME.
    Ann Hematol; 2005 Oct 01; 84(10):650-5. PubMed ID: 15986199
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  • 39. 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 Oct 01; 25(5-6):354-7. PubMed ID: 10660483
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  • 40. Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods.
    Milman N, Koefoed P, Pedersen P, Nielsen FC, Eiberg H.
    Eur J Haematol; 2003 Dec 01; 71(6):403-7. PubMed ID: 14703688
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