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Journal Abstract Search

99 related items for PubMed ID: 12651261

  • 41. Hereditary hemochromatosis: the clinical significance of the S65C mutation.
    Asberg A, Thorstensen K, Hveem K, Bjerve KS.
    Genet Test; 2002; 6(1):59-62. PubMed ID: 12180078
    [Abstract] [Full Text] [Related]

  • 42. A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology.
    Restagno G, Gomez AM, Sbaiz L, De Gobbi M, Roetto A, Bertino E, Fabris C, Fiorucci GC, Fortina P, Camaschella C.
    Genet Test; 2000; 4(2):177-81. PubMed ID: 10953958
    [Abstract] [Full Text] [Related]

  • 43. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M, de Salamanca RE, Morales P, Martínez-Laso J, Fontanellas A, Castro MJ, Rojo R, Moscoso J, Zamora J, Serrano-Vela JI, Arnaiz-Villena A.
    J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
    [Abstract] [Full Text] [Related]

  • 44. Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait.
    Garewal G, Das R, Ahluwalia J, Marwaha RK.
    Eur J Haematol; 2005 Apr; 74(4):333-6. PubMed ID: 15777346
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  • 45. Multicentric origin of hemochromatosis gene (HFE) mutations.
    Rochette J, Pointon JJ, Fisher CA, Perera G, Arambepola M, Arichchi DS, De Silva S, Vandwalle JL, Monti JP, Old JM, Merryweather-Clarke AT, Weatherall DJ, Robson KJ.
    Am J Hum Genet; 1999 Apr; 64(4):1056-62. PubMed ID: 10090890
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  • 46. Prevalence of HFE C282Y and H63D in Jewish populations and clinical implications of H63D homozygosity.
    Matas M, Guix P, Castro JA, Parera M, Ramon MM, Obrador A, Picornell A.
    Clin Genet; 2006 Feb; 69(2):155-62. PubMed ID: 16433696
    [Abstract] [Full Text] [Related]

  • 47. Prevalence and clinical implications of HFE gene mutations (C282Y and H63D) in patients with chronic hepatitis B and C in Taiwan.
    Mah YH, Kao JH, Liu CJ, Chen CL, Chen PJ, Lai MY, Chen DS.
    Liver Int; 2005 Apr; 25(2):214-9. PubMed ID: 15780041
    [Abstract] [Full Text] [Related]

  • 48. HFE gene mutations, hepatic iron content, and histological severity in hepatitis C virus-induced chronic hepatitis.
    Ladero JM, Ropero P, Ortega L, Taxonera C, González FA, López-Alonso G, Briceño O, Rodríguez-Agulló JL, González L, Villegas A, Díaz-Rubio M.
    Rev Esp Enferm Dig; 2003 Dec; 95(12):829-36. PubMed ID: 14972004
    [Abstract] [Full Text] [Related]

  • 49. Prevalence of H63D, S65C and C282Y mutations of the HFE gene in 1120 voluntary blood donors from Antioquia region of northwest Colombia.
    Avila-Gomez IC, Aristizabal-Bernal B, Jimenez-Del-Rio M, Velez-Pardo C.
    Blood Cells Mol Dis; 2008 Dec; 40(3):449-51. PubMed ID: 18289891
    [No Abstract] [Full Text] [Related]

  • 50. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.
    Schweiz Med Wochenschr; 2000 Aug 08; 130(31-32):1112-9. PubMed ID: 11008304
    [Abstract] [Full Text] [Related]

  • 51. 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]

  • 52. Comparative study of the two more frequent HFE mutations (C282Y and H63D): significant different allelic frequencies between the North and South of Portugal.
    Cardoso CS, Oliveira P, Porto G, Oberkanins C, Mascarenhas M, Rodrigues P, Kury F, de Sousa M.
    Eur J Hum Genet; 2001 Nov 21; 9(11):843-8. PubMed ID: 11781701
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  • 58. Haplotype analysis of the H63D, IVS2+4t/c, and C282Y polymorphisms of the HFE gene reveals rare events of intragenic recombination.
    Curcio M, Fornaciari S, Mariotti ML, Chelazzi S, Scatena F, Presciuttini S.
    Eur J Haematol; 2008 Apr 21; 80(4):341-5. PubMed ID: 18182079
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  • 59. Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis.
    Rubio JP, Bahlo M, Tubridy N, Stankovich J, Burfoot R, Butzkueven H, Chapman C, Johnson L, Marriott M, Mraz G, Tait B, Wilkinson C, Taylor B, Speed TP, Foote SJ, Kilpatrick TJ.
    Hum Genet; 2004 May 21; 114(6):573-80. PubMed ID: 15014978
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