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Journal Abstract Search

169 related items for PubMed ID: 8707280

  • 1. The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients.
    Piperno A, Arosio C, Fargion S, Roetto A, Nicoli C, Girelli D, Sbaiz L, Gasparini P, Boari G, Sampietro M, Camaschella C.
    Hepatology; 1996 Jul; 24(1):43-6. PubMed ID: 8707280
    [Abstract] [Full Text] [Related]

  • 2. 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 Jul; 34(1):38-47. PubMed ID: 15607698
    [Abstract] [Full Text] [Related]

  • 3. The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda.
    Roberts AG, Whatley SD, Nicklin S, Worwood M, Pointon JJ, Stone C, Elder GH.
    Hepatology; 1997 Jan; 25(1):159-61. PubMed ID: 8985283
    [Abstract] [Full Text] [Related]

  • 4. Relationship between genotype, assessed by HLA typing, and phenotypic expression of iron status markers in families of 29 probands with hereditary haemochromatosis.
    Milman N, Fenger K, Graudal NA, Nielsen LS.
    Dan Med Bull; 1994 Jun; 41(3):366-70. PubMed ID: 7924465
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Allelic associations and homozygosity at loci from HLA-B to D6S299 in genetic haemochromatosis.
    Raha-Chowdhury R, Bowen DJ, Burnett AK, Worwood M.
    J Med Genet; 1995 Jun 01; 32(6):446-52. PubMed ID: 7666396
    [Abstract] [Full Text] [Related]

  • 7. Hemochromatosis: association of severity of iron overload with genetic markers.
    Barton JC, Harmon L, Rivers C, Acton RT.
    Blood Cells Mol Dis; 1996 Jun 01; 22(3):195-204. PubMed ID: 9075570
    [Abstract] [Full Text] [Related]

  • 8. HLA determinants in idiopathic haemochromatosis.
    Milman N, Graudal N, Nielsen LS, Sørensen SA.
    Dan Med Bull; 1985 Oct 01; 32(5):262-4. PubMed ID: 4053696
    [Abstract] [Full Text] [Related]

  • 9. Clinical and biochemical abnormalities in people heterozygous for hemochromatosis.
    Bulaj ZJ, Griffen LM, Jorde LB, Edwards CQ, Kushner JP.
    N Engl J Med; 1996 Dec 12; 335(24):1799-805. PubMed ID: 8943161
    [Abstract] [Full Text] [Related]

  • 10. Expression of hemochromatosis in homozygous subjects. Implications for early diagnosis and prevention.
    Powell LW, Summers KM, Board PG, Axelsen E, Webb S, Halliday JW.
    Gastroenterology; 1990 Jun 12; 98(6):1625-32. PubMed ID: 2338199
    [Abstract] [Full Text] [Related]

  • 11. [Idiopathic hemochromatosis. Immunogenetics and diagnosis. Prevention by HLA genotypes].
    Fauchet R, Lemignon L, Bourel M, Genetet B, Simon M.
    Pathol Biol (Paris); 1986 Jun 12; 34(6):715-21. PubMed ID: 3531987
    [Abstract] [Full Text] [Related]

  • 12. Histocompatibility antigens as markers of abnormal iron metabolism in idiopathic hemochromatosis.
    Lloyd DA, Adams P, Sinclair NR, Stiller CR, Valberg LS.
    Can Med Assoc J; 1978 Nov 04; 119(9):1051-6. PubMed ID: 84705
    [Abstract] [Full Text] [Related]

  • 13. The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?
    Olsson KS, Ritter B, Hansson N.
    Eur J Haematol; 2007 Nov 04; 79(5):429-34. PubMed ID: 17924859
    [Abstract] [Full Text] [Related]

  • 14. [Long-term survival of 2 cases of hemochromatosis respectively homozygous for His63Asp and Cys282Tyr mutations].
    Samii K, Darbellay R, Trachsel H, Beris P.
    Schweiz Med Wochenschr; 1997 Nov 08; 127(45):1867-70. PubMed ID: 9446207
    [Abstract] [Full Text] [Related]

  • 15. Localization of Type 1 Diabetes susceptibility in the ancestral haplotype 18.2 by high density SNP mapping.
    Santiago JL, Li W, Lee A, Martinez A, Chandrasekaran A, Fernandez-Arquero M, Khalili H, de la Concha EG, Urcelay E, Gregersen PK.
    Genomics; 2009 Oct 08; 94(4):228-32. PubMed ID: 19591919
    [Abstract] [Full Text] [Related]

  • 16. HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity.
    Barton JC, Barton JC, Acton RT.
    Hereditas; 2022 Jun 06; 159(1):25. PubMed ID: 35659379
    [Abstract] [Full Text] [Related]

  • 17. Hereditary hemochromatosis. Phenotypic expression of the disease.
    Cartwright GE, Edwards CQ, Kravitz K, Skolnick M, Amos DB, Johnson A, Buskjaer L.
    N Engl J Med; 1979 Jul 26; 301(4):175-9. PubMed ID: 449974
    [Abstract] [Full Text] [Related]

  • 18. Genetic and phenotypic expression of hemochromatosis in Canadians.
    Borwein ST, Ghent CN, Flanagan PR, Chamberlain MJ, Valberg LS.
    Clin Invest Med; 1983 Jul 26; 6(3):171-9. PubMed ID: 6652983
    [Abstract] [Full Text] [Related]

  • 19. DNA typing of the HLA-A, -B and -C genes: possible MHC class I haplotypes in the northeastern-Thais.
    Romphruk A, Leelayuwat C, Barusrux S, Puapairoj C, Romphruk A, Urwijitaroon Y.
    J Med Assoc Thai; 1997 Sep 26; 80 Suppl 1():S13-9. PubMed ID: 9347640
    [Abstract] [Full Text] [Related]

  • 20. Usefulness of erythrocyte ferritin analysis in hereditary hemochromatosis.
    Cruickshank MK, Ninness J, Curtis A, Barr RM, Flanagan PR, Ghent CN, Valberg LS.
    CMAJ; 1987 Jun 15; 136(12):1259-64. PubMed ID: 3472636
    [Abstract] [Full Text] [Related]

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