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208 related items for PubMed ID: 19656448

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

  • 22. 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 Feb; 49(12):651-655. PubMed ID: 15538648
    [Abstract] [Full Text] [Related]

  • 23. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE, Hutzler S, Bollheimer LC, Buettner R, Hellerbrand C, Schöelmerich J, Palitzsch KD.
    Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
    [Abstract] [Full Text] [Related]

  • 24. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.
    Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D.
    Med Sci Monit; 2011 Oct; 17(10):CR552-6. PubMed ID: 21959608
    [Abstract] [Full Text] [Related]

  • 25. 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 Oct; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

  • 26. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL, Ou CY, Cappuccio J, Braggins C, Dunnigan K, Phatak PD.
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 27. Simultaneous detection of the C282Y, H63D and S65C mutations in the hemochromatosis gene using quenched-FRET real-time PCR.
    Moysés CB, Moreira ES, Asprino PF, Guimarães GS, Alberto FL.
    Braz J Med Biol Res; 2008 Oct; 41(10):833-8. PubMed ID: 19030706
    [Abstract] [Full Text] [Related]

  • 28. Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C.
    Sumner K, Hubley L, Pont-Kingdon G, Mitchell S, Wayman T, Wilson A, Meadows C, Elenitoba-Johnson K, Pattison D, Dobrowolski S, Best H, Lyon E.
    Genet Test Mol Biomarkers; 2012 Jul; 16(7):656-60. PubMed ID: 22364140
    [Abstract] [Full Text] [Related]

  • 29. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
    Larsen LE, Ellervik C, Appleyard M, Nordestgaard BG, Birgens H, Tybjaerg-Hansen A.
    Ugeskr Laeger; 2002 Sep 23; 164(39):4545-7. PubMed ID: 12380399
    [Abstract] [Full Text] [Related]

  • 30. 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 23; 70(4):294-300. PubMed ID: 17767550
    [Abstract] [Full Text] [Related]

  • 31. 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 23; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 32. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
    De Marco F, Liguori R, Giardina MG, D'Armiento M, Angelucci E, Lucariello A, Morante R, Cimino L, Galeota-Lanza A, Tarantino G, Ascione A, Budillon G, Vecchione R, Martinelli R, Matarazzo M, De Simone V.
    Clin Chem Lab Med; 2004 Jan 23; 42(1):17-24. PubMed ID: 15061375
    [Abstract] [Full Text] [Related]

  • 33. S65C and other mutations in the haemochromatosis gene in the Czech population.
    Cimburová M, Půtová I, Provazníková H, Pintérová D, Horák J.
    Folia Biol (Praha); 2005 Jan 23; 51(6):172-6. PubMed ID: 16419611
    [Abstract] [Full Text] [Related]

  • 34. Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands.
    Milman N, á Steig T, Koefoed P, Pedersen P, Fenger K, Nielsen FC.
    Ann Hematol; 2005 Mar 23; 84(3):146-9. PubMed ID: 15042317
    [Abstract] [Full Text] [Related]

  • 35. 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 Mar 23; 8(4):407-10. PubMed ID: 15684872
    [Abstract] [Full Text] [Related]

  • 36. Contribution of the H63D mutation in HFE to murine hereditary hemochromatosis.
    Tomatsu S, Orii KO, Fleming RE, Holden CC, Waheed A, Britton RS, Gutierrez MA, Velez-Castrillon S, Bacon BR, Sly WS.
    Proc Natl Acad Sci U S A; 2003 Dec 23; 100(26):15788-93. PubMed ID: 14673107
    [Abstract] [Full Text] [Related]

  • 37. Common heterozygous hemochromatosis gene mutations are risk factors for inflammation and fibrosis in chronic hepatitis C.
    Geier A, Reugels M, Weiskirchen R, Wasmuth HE, Dietrich CG, Siewert E, Gartung C, Lorenzen J, Bosserhoff AK, Brügmann M, Gressner AM, Matern S, Lammert F.
    Liver Int; 2004 Aug 23; 24(4):285-94. PubMed ID: 15287851
    [Abstract] [Full Text] [Related]

  • 38. Pathogenesis of hereditary hemochromatosis: genetics and beyond.
    Britton RS, Fleming RE, Parkkila S, Waheed A, Sly WS, Bacon BR.
    Semin Gastrointest Dis; 2002 Apr 23; 13(2):68-79. PubMed ID: 12064862
    [Abstract] [Full Text] [Related]

  • 39. 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 Apr 23; 47(4):325-30. PubMed ID: 15581829
    [Abstract] [Full Text] [Related]

  • 40. 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 23; 84(10):650-5. PubMed ID: 15986199
    [Abstract] [Full Text] [Related]

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