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Journal Abstract Search

172 related items for PubMed ID: 12547216

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. Association between the HFE mutations and longevity: a study in Sardinian population.
    Carru C, Pes GM, Deiana L, Baggio G, Franceschi C, Lio D, Balistreri CR, Candore G, Colonna-Romano G, Caruso C.
    Mech Ageing Dev; 2003 Apr; 124(4):529-32. PubMed ID: 12714263
    [Abstract] [Full Text] [Related]

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

  • 24. 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; 84(12):802-6. PubMed ID: 15995871
    [Abstract] [Full Text] [Related]

  • 25. Frequency and biochemical expression of C282Y/H63D hemochromatosis (HFE) gene mutations in the healthy adult population in Italy.
    Cassanelli S, Pignatti E, Montosi G, Garuti C, Mariano M, Campioli D, Carbonieri A, Baldini E, Pietrangelo A.
    J Hepatol; 2001 Apr; 34(4):523-8. PubMed ID: 11394651
    [Abstract] [Full Text] [Related]

  • 26. Prevalence of HFE mutations in upper Northern Italy: study of 1132 unrelated blood donors.
    Mariani R, Salvioni A, Corengia C, Erba N, Lanzafame C, De Micheli V, Baldini V, Arosio C, Fossati L, Trombini P, Oberkanins C, Piperno A.
    Dig Liver Dis; 2003 Jul; 35(7):479-81. PubMed ID: 12870733
    [Abstract] [Full Text] [Related]

  • 27. HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis.
    Mura C, Raguenes O, Férec C.
    Blood; 1999 Apr 15; 93(8):2502-5. PubMed ID: 10194428
    [Abstract] [Full Text] [Related]

  • 28. Hemochromatosis in Ireland and HFE.
    Ryan E, O'keane C, Crowe J.
    Blood Cells Mol Dis; 1998 Dec 15; 24(4):428-32. PubMed ID: 9851896
    [Abstract] [Full Text] [Related]

  • 29. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E, Cerani P, Rolandi V, Rovati A, Bergamaschi G.
    Haematologica; 2000 Aug 15; 85(8):787-91. PubMed ID: 10942923
    [Abstract] [Full Text] [Related]

  • 30. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Aug 15; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

  • 31. 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 Aug 15; 4(6):436-40. PubMed ID: 14671617
    [Abstract] [Full Text] [Related]

  • 32. Analysis of HFE genes C282Y, H63D, and S65D in patients with hyperferritinemia from northeastern Brazil.
    Leão GD, Freire JM, Cunha Fernandes AL, Moura de Oliveira TM, Leão ND, Gil EA, de Vasconcelos RC, Azevedo JP, de Farias Sales VS, de Araújo Moura Lemos TM, Leão MD, do Nascimento FF, Maciel JF, de Freitas RV, de Souza Paiva A, Cavalcanti GB.
    J Clin Lab Anal; 2014 May 15; 28(3):178-85. PubMed ID: 24395214
    [Abstract] [Full Text] [Related]

  • 33. 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 15; 84(10):646-9. PubMed ID: 15871018
    [Abstract] [Full Text] [Related]

  • 34. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in 2501 ethnic Danes.
    Milman N, Pedersen P, Ovesen L, Melsen GV, Fenger K.
    Ann Hematol; 2004 Oct 15; 83(10):654-7. PubMed ID: 15141324
    [Abstract] [Full Text] [Related]

  • 35. HLA haplotypes associated with hemochromatosis mutations in the Spanish population.
    Pacho A, Mancebo E, del Rey MJ, Castro MJ, Oliver D, García-Berciano M, González L, Morales P.
    BMC Med Genet; 2004 Oct 21; 5():25. PubMed ID: 15498100
    [Abstract] [Full Text] [Related]

  • 36. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 21; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 37. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J, González Quintela A, Fernández de Trocóniz LL, Barros Angueira F, Pérez-Quintela BV, Pérez Becerra E, Martínez de Rituerto ST, Otero Antón E, Torre Carballada JA.
    Rev Clin Esp; 2002 Oct 21; 202(10):534-9. PubMed ID: 12361551
    [Abstract] [Full Text] [Related]

  • 38. 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 21; 88(4):396-401. PubMed ID: 12681966
    [Abstract] [Full Text] [Related]

  • 39. Frequency of the hemochromatosis C282Y and H63D mutations in a Polish population of Slavic origin.
    Moczulski DK, Grzeszczak W, Gawlik B.
    Med Sci Monit; 2001 Apr 21; 7(3):441-3. PubMed ID: 11386022
    [Abstract] [Full Text] [Related]

  • 40. The role of HFE mutations on iron metabolism in beta-thalassemia carriers.
    Martins R, Picanço I, Fonseca A, Ferreira L, Rodrigues O, Coelho M, Seixas T, Miranda A, Nunes B, Costa L, Romão L, Faustino P.
    J Hum Genet; 2004 Apr 21; 49(12):651-655. PubMed ID: 15538648
    [Abstract] [Full Text] [Related]

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