These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

411 related items for PubMed ID: 16509978

  • 1. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
    Cruz E, Vieira J, Almeida S, Lacerda R, Gartner A, Cardoso CS, Alves H, Porto G.
    BMC Med Genet; 2006 Mar 01; 7():16. PubMed ID: 16509978
    [Abstract] [Full Text] [Related]

  • 2. Low serum transferrin levels in HFE C282Y homozygous subjects are associated with low CD8(+) T lymphocyte numbers.
    Macedo MF, Cruz E, Lacerda R, Porto G, de Sousa M.
    Blood Cells Mol Dis; 2005 Mar 01; 35(3):319-25. PubMed ID: 16140024
    [Abstract] [Full Text] [Related]

  • 3. Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas.
    Costa M, Cruz E, Barton JC, Thorstensen K, Morais S, da Silva BM, Pinto JP, Vieira CP, Vieira J, Acton RT, Porto G.
    PLoS One; 2013 Mar 01; 8(11):e79990. PubMed ID: 24282517
    [Abstract] [Full Text] [Related]

  • 4. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC, Wiener HW, Acton RT, Go RC.
    Blood Cells Mol Dis; 2005 Mar 01; 34(1):38-47. PubMed ID: 15607698
    [Abstract] [Full Text] [Related]

  • 5. Involvement of the major histocompatibility complex region in the genetic regulation of circulating CD8 T-cell numbers in humans.
    Cruz E, Vieira J, Gonçalves R, Alves H, Almeida S, Rodrigues P, Lacerda R, Porto G.
    Tissue Antigens; 2004 Jul 01; 64(1):25-34. PubMed ID: 15191520
    [Abstract] [Full Text] [Related]

  • 6. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects.
    Cruz E, Melo G, Lacerda R, Almeida S, Porto G.
    Blood Cells Mol Dis; 2006 Jul 01; 37(1):33-9. PubMed ID: 16762569
    [Abstract] [Full Text] [Related]

  • 7. A new 500 kb haplotype associated with high CD8+ T-lymphocyte numbers predicts a less severe expression of hereditary hemochromatosis.
    Cruz E, Whittington C, Krikler SH, Mascarenhas C, Lacerda R, Vieira J, Porto G.
    BMC Med Genet; 2008 Nov 06; 9():97. PubMed ID: 18990219
    [Abstract] [Full Text] [Related]

  • 8. A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans.
    Vieira J, Cardoso CS, Pinto J, Patil K, Brazdil P, Cruz E, Mascarenhas C, Lacerda R, Gartner A, Almeida S, Alves H, Porto G.
    Int J Immunogenet; 2007 Oct 06; 34(5):359-67. PubMed ID: 17845307
    [Abstract] [Full Text] [Related]

  • 9. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G, Cardoso CS, Gordeuk V, Cruz E, Fraga J, Areias J, Oliveira JC, Bravo F, Gangaidzo IT, MacPhail AP, Gomo ZA, Moyo VM, Melo G, Silva C, Justiça B, de Sousa M.
    Eur J Haematol; 2001 Aug 06; 67(2):110-8. PubMed ID: 11722599
    [Abstract] [Full Text] [Related]

  • 10. Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis.
    Porto G, Alves H, Rodrigues P, Cabeda JM, Portal C, Ruivo A, Justiça B, Wolff R, De Sousa M.
    Immunogenetics; 1998 Apr 06; 47(5):404-10. PubMed ID: 9510559
    [Abstract] [Full Text] [Related]

  • 11. Linkage disequilibrium analysis in Australian haemochromatosis patients indicates bipartite association with clinical expression.
    Pratiwi R, Fletcher LM, Pyper WR, Do KA, Crawford DH, Powell LW, Jazwinska EC.
    J Hepatol; 1999 Jul 06; 31(1):39-46. PubMed ID: 10424281
    [Abstract] [Full Text] [Related]

  • 12. Hepatic iron overload: direct HFE (HLA-H) mutation analysis vs quantitative iron assays for the diagnosis of hereditary hemochromatosis.
    Press RD, Flora K, Gross C, Rabkin JM, Corless CL.
    Am J Clin Pathol; 1998 May 06; 109(5):577-84. PubMed ID: 9576576
    [Abstract] [Full Text] [Related]

  • 13. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Adams PC, Pankow JS, Barton JC, Acton RT, Leiendecker-Foster C, McLaren GD, Speechley M, Eckfeldt JH.
    Circ Cardiovasc Genet; 2009 Feb 06; 2(1):34-7. PubMed ID: 20031565
    [Abstract] [Full Text] [Related]

  • 14. 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 06; 35(3):329-35. PubMed ID: 11887210
    [Abstract] [Full Text] [Related]

  • 15. Iron loading in HFE p.C282Y homozygotes found by population screening: relationships to HLA-type and T-lymphocyte subsets.
    Thorstensen K, Kvitland MA, Irgens WØ, Åsberg A, Borch-Iohnsen B, Moen T, Hveem K.
    Scand J Clin Lab Invest; 2017 Nov 06; 77(7):477-485. PubMed ID: 28678636
    [Abstract] [Full Text] [Related]

  • 16. Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping.
    Barton JC, Barton JC, Acton RT.
    Eur J Haematol; 2010 Nov 06; 85(5):439-47. PubMed ID: 20722701
    [Abstract] [Full Text] [Related]

  • 17. Co-selection of the H63D mutation and the HLA-A29 allele: a new paradigm of linkage disequilibrium?
    Cardoso CS, Alves H, Mascarenhas M, Gonçalves R, Oliveira P, Rodrigues P, Cruz E, de Sousa M, Porto G.
    Immunogenetics; 2002 Mar 06; 53(12):1002-8. PubMed ID: 11904676
    [Abstract] [Full Text] [Related]

  • 18. 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 06; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 19. Hepatic damage in C282Y homozygotes relates to low numbers of CD8+ cells in the liver lobuli.
    Cardoso EM, Hagen K, de Sousa M, Hultcrantz R.
    Eur J Clin Invest; 2001 Jan 06; 31(1):45-53. PubMed ID: 11168438
    [Abstract] [Full Text] [Related]

  • 20. Increased capacity of lymphocytes from hereditary hemochromatosis patients homozygous for the C282Y HFE mutation to respond to the genotoxic effect of diepoxybutane.
    Porto B, Vieira R, Porto G.
    Mutat Res; 2009 Feb 19; 673(1):37-42. PubMed ID: 19146986
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.