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Journal Abstract Search

222 related items for PubMed ID: 12942784

  • 21. 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; 8(4):407-10. PubMed ID: 15684872
    [Abstract] [Full Text] [Related]

  • 22. 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; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 23. The ethnospecific distribution of the HFE haplotypes for IVS2(+4)t/c, IVS4(-44)t/c, and IVS5(-47)g/a in populations of Russia and possible effects of these single-nucleotide polymorphisms in splicing.
    Mikhailova SV, Babenko VN, Voevoda MI, Romashchenko AG.
    Genet Test Mol Biomarkers; 2010 Aug; 14(4):461-9. PubMed ID: 20642366
    [Abstract] [Full Text] [Related]

  • 24. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M, Putova I, Provaznikova H, Horak J.
    Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
    [Abstract] [Full Text] [Related]

  • 25. 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; 30(3):555-7. PubMed ID: 17058523
    [Abstract] [Full Text] [Related]

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

  • 27. Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis.
    Canavese C, Bergamo D, Barbieri S, Timbaldi M, Thea A, Martina G, Damiani D, Fenoglio R, Donati-Marella B, Priolo G.
    Clin Nephrol; 2002 Dec; 58(6):438-44. PubMed ID: 12508966
    [Abstract] [Full Text] [Related]

  • 28. Association of porphyria cutanea tarda with hereditary hemochromatosis.
    Mehrany K, Drage LA, Brandhagen DJ, Pittelkow MR.
    J Am Acad Dermatol; 2004 Aug; 51(2):205-11. PubMed ID: 15280838
    [Abstract] [Full Text] [Related]

  • 29. Significance of H63D homozygosity in a Basque population with hemochromatosis.
    Castiella A, Zapata E, de Juan MD, Otazua P, Fernandez J, Zubiaurre L, Arriola JA, Gipuzkoa Hemochromatosis Group.
    J Gastroenterol Hepatol; 2010 Jul; 25(7):1295-8. PubMed ID: 20594259
    [Abstract] [Full Text] [Related]

  • 30. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.
    Aranda N, Viteri FE, Montserrat C, Arija V.
    Ann Hematol; 2010 Aug; 89(8):767-73. PubMed ID: 20107990
    [Abstract] [Full Text] [Related]

  • 31. Frequency of the C282Y and H63D mutations of the hemochromatosis gene (HFE) in a cohort of 1,000 neonates in Madrid (Spain).
    Ropero P, Briceño O, Mateo M, Polo M, Mora A, González FA, Villegas A.
    Ann Hematol; 2006 May; 85(5):323-6. PubMed ID: 16520984
    [Abstract] [Full Text] [Related]

  • 32. [Mutations of hemochromatosis gene in volunteer blood donors and Chilean porphyria cutanea tarda patients].
    Wolff CF, Armas RM, Frank J, Poblete PG.
    Medicina (B Aires); 2006 May; 66(5):421-6. PubMed ID: 17137171
    [Abstract] [Full Text] [Related]

  • 33. Prevalence of three hereditary hemochromatosis mutant alleles in the Michigan Caucasian population.
    Barry E, Derhammer T, Elsea SH.
    Community Genet; 2005 May; 8(3):173-9. PubMed ID: 16113534
    [Abstract] [Full Text] [Related]

  • 34. 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]

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

  • 36. Genetic hemochromatosis, a Celtic disease: is it now time for population screening?
    Byrnes V, Ryan E, Barrett S, Kenny P, Mayne P, Crowe J.
    Genet Test; 2001 Dec; 5(2):127-30. PubMed ID: 11551098
    [Abstract] [Full Text] [Related]

  • 37. [Analysis of the hemochromatosis gene (HFE) mutations, C282Y and H63D, in the populations of Central Asia].
    Khusainova RI, Khusnutdinova NN, Khusnutdinova EK.
    Genetika; 2006 Mar; 42(3):421-6. PubMed ID: 16649670
    [Abstract] [Full Text] [Related]

  • 38. Analysis of HFE-codon 63/282 (H63D/C282Y) gene variants in mexican mestizos. Blood donors and patients with hereditary hemochromatosis.
    Ruiz-Argüelles GJ, Garcés-Eisele J, Gelbart T, Monroy-Barreto M, Reyes-Núñez V, Juárez-Morales JL, de Lourdes González-Garrido M, Ramírez-Cisneros FJ, Gallegos-Antúnez D.
    Arch Med Res; 2000 Mar; 31(4):422-4. PubMed ID: 11068087
    [Abstract] [Full Text] [Related]

  • 39. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City.
    Baptista-González HA, Rosenfeld-Mann F, Trueba-Gómez R, Bermejo-Martínez L, Méndez-Sánchez N.
    Ann Hepatol; 2007 Mar; 6(1):55-60. PubMed ID: 17297430
    [Abstract] [Full Text] [Related]

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