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Journal Abstract Search

97 related items for PubMed ID: 17160266

  • 21.
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  • 22. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC, Cançado RD, Pereira AC, Schettert IT, Soares RA, Pagliusi RA, Hirata RD, Hirata MH, Teixeira AC, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2011 Apr 15; 46(4):302-7. PubMed ID: 21411349
    [Abstract] [Full Text] [Related]

  • 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 15; 35(3):329-35. PubMed ID: 11887210
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  • 24. 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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  • 25.
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  • 26. 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 Aug 15; 47(4):325-30. PubMed ID: 15581829
    [Abstract] [Full Text] [Related]

  • 27. 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 15; 7(1):103-8. PubMed ID: 15642540
    [Abstract] [Full Text] [Related]

  • 28. Prevalence of hemochromatosis gene (HFE) mutations in Greece.
    Papazoglou D, Exiara T, Speletas M, Panagopoulos I, Maltezos E.
    Acta Haematol; 2003 Jan 15; 109(3):137-40. PubMed ID: 12714823
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  • 29.
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  • 30. [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 15; 30(4):223-8. PubMed ID: 19731820
    [Abstract] [Full Text] [Related]

  • 31. Mutation analysis of the HFE gene associated with hereditary hemochromatosis in a Venezuelan sample.
    Vizzi E, Loureiro CL, Gerder M, de las Nieves Garcia-Casal M, Rodríguez-Larralde A, Gerace L, Ludert JE, Liprandi F, Pujol FH.
    Ann Hematol; 2005 Nov 15; 84(12):802-6. PubMed ID: 15995871
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  • 32.
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  • 33. 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 15; 84(10):650-5. PubMed ID: 15986199
    [Abstract] [Full Text] [Related]

  • 34. 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 Oct 15; 16(6):309-10. PubMed ID: 14765621
    [Abstract] [Full Text] [Related]

  • 35. Frequency of HFE gene mutations C282Y and H63D in Bosnia and Herzegovina.
    Terzić R, Sehić A, Teran N, Terzić I, Peterlin B.
    Coll Antropol; 2006 Sep 15; 30(3):555-7. PubMed ID: 17058523
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  • 36. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 15; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 37. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
    Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R.
    Haematologica; 2002 Mar 15; 87(3):242-5. PubMed ID: 11869934
    [Abstract] [Full Text] [Related]

  • 38. HFE gene mutations in patients with altered iron metabolism in Argentina.
    Rossetti MV, Méndez M, Afonso S, Gerez E, Batlle A, Muñoz A, Parera V.
    Cell Mol Biol (Noisy-le-grand); 2009 Jul 01; 55(2):31-5. PubMed ID: 19656448
    [Abstract] [Full Text] [Related]

  • 39. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D, Legler T, Lynen R, Addicks N, Ramadori G.
    Z Gastroenterol; 2003 Nov 01; 41(11):1069-76. PubMed ID: 14648375
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  • 40. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
    Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.
    Ann Hematol; 2005 Oct 01; 84(10):646-9. PubMed ID: 15871018
    [Abstract] [Full Text] [Related]

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