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Journal Abstract Search

161 related items for PubMed ID: 27561698

  • 21. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M, Vaupotic T, Rupreht R, Curin-Serbec V.
    BMC Med Genet; 2007 Nov 23; 8():69. PubMed ID: 18036208
    [Abstract] [Full Text] [Related]

  • 22. Frequency of Hereditary Hemochromatosis Gene (HFE) Variants in Sri Lankan Transfusion-Dependent Beta-Thalassemia Patients and Their Association With the Serum Ferritin Level.
    Padeniya P, Goonasekara H, Abeysekera G, Jayasekara R, Dissanayake V.
    Front Pediatr; 2022 Nov 23; 10():890989. PubMed ID: 35903164
    [Abstract] [Full Text] [Related]

  • 23. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA, Carter K, Darke C, Guttridge MG, Ravine D, Hutton RD, Napier JA, Worwood M.
    Br J Haematol; 2001 Aug 23; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 24. HFE Gene Mutations and Iron Status in 100 Healthy Polish Children.
    Kaczorowska-Hac B, Luszczyk M, Antosiewicz J, Ziolkowski W, Adamkiewicz-Drozynska E, Mysliwiec M, Milosz E, Kaczor JJ.
    J Pediatr Hematol Oncol; 2017 Jul 23; 39(5):e240-e243. PubMed ID: 28406842
    [Abstract] [Full Text] [Related]

  • 25. H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers.
    Yamsri S, Sanchaisuriya K, Fucharoen S, Fucharoen G, Jetsrisuparb A, Wiangnon S, Changtrakul Y, Sanchaisuriya P.
    Acta Haematol; 2007 Jul 23; 118(2):99-105. PubMed ID: 17637512
    [Abstract] [Full Text] [Related]

  • 26. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
    Njajou OT, Houwing-Duistermaat JJ, Osborne RH, Vaessen N, Vergeer J, Heeringa J, Pols HA, Hofman A, van Duijn CM.
    Eur J Hum Genet; 2003 Mar 23; 11(3):225-31. PubMed ID: 12673276
    [Abstract] [Full Text] [Related]

  • 27. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
    Silva B, Pita L, Gomes S, Gonçalves J, Faustino P.
    Ann Hematol; 2014 Dec 23; 93(12):2063-6. PubMed ID: 25015054
    [Abstract] [Full Text] [Related]

  • 28. HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions.
    Sharma V, Panigrahi I, Dutta P, Tyagi S, Choudhry VP, Saxena R.
    Indian J Pathol Microbiol; 2007 Jan 23; 50(1):82-5. PubMed ID: 17474269
    [Abstract] [Full Text] [Related]

  • 29. 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 Jan 23; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 30. Iron overload phenotypes and HFE genotypes in white hemochromatosis and iron overload screening study participants without HFE p.C282Y/p.C282Y.
    Barton JC, Barton JC, Acton RT.
    PLoS One; 2022 Jan 23; 17(7):e0271973. PubMed ID: 35895739
    [Abstract] [Full Text] [Related]

  • 31. [Iron intake and HFE gen in male adults from Buenos Aires].
    Felipoff AL, Fleischman SJ, Donadío ML, Sebastiano V, Castro M, Vellicce A, Rey JA, Lardo MM, Langini SH.
    Medicina (B Aires); 2017 Jan 23; 77(6):458-464. PubMed ID: 29223935
    [Abstract] [Full Text] [Related]

  • 32. HFE Genotype, Ferritin Levels and Transferrin Saturation in Patients with Suspected Hereditary Hemochromatosis.
    Sandnes M, Vorland M, Ulvik RJ, Reikvam H.
    Genes (Basel); 2021 Jul 28; 12(8):. PubMed ID: 34440336
    [Abstract] [Full Text] [Related]

  • 33. 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 28; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 34. 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 28; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 35. 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 28; 84(12):802-6. PubMed ID: 15995871
    [Abstract] [Full Text] [Related]

  • 36. Hereditary hemochromatosis in north-eastern Romania.
    Voicu PM, Cojocariu C, Petrescu-Dănilă E, Stanciu C, Covic M, Rusu M, Trifan A.
    Rev Med Chir Soc Med Nat Iasi; 2010 Nov 28; 114(4):982-7. PubMed ID: 21495455
    [Abstract] [Full Text] [Related]

  • 37. HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology.
    Hanson EH, Imperatore G, Burke W.
    Am J Epidemiol; 2001 Aug 01; 154(3):193-206. PubMed ID: 11479183
    [Abstract] [Full Text] [Related]

  • 38. Late-onset Hemochromatosis: Co-inheritance of β-thalassemia and Hereditary Hemochromatosis in a Chinese Family: A Case Report and Epidemiological Analysis of Diverse Populations.
    Yang J, Lun Y, Shuai X, Liu T, Wu Y.
    Intern Med; 2018 Dec 01; 57(23):3433-3438. PubMed ID: 28943547
    [Abstract] [Full Text] [Related]

  • 39. A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation.
    Gochee PA, Powell LW, Cullen DJ, Du Sart D, Rossi E, Olynyk JK.
    Gastroenterology; 2002 Mar 01; 122(3):646-51. PubMed ID: 11874997
    [Abstract] [Full Text] [Related]

  • 40. 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 01; 70(4):294-300. PubMed ID: 17767550
    [Abstract] [Full Text] [Related]

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