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Journal Abstract Search

518 related items for PubMed ID: 11479183

  • 1. 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]

  • 2. Geographic and racial/ethnic differences in HFE mutation frequencies in the Hemochromatosis and Iron Overload Screening (HEIRS) Study.
    Acton RT, Barton JC, Snively BM, McLaren CE, Adams PC, Harris EL, Speechley MR, McLaren GD, Dawkins FW, Leiendecker-Foster C, Holup JL, Balasubramanyam A, Hemochromatosis and Iron Overload Screening Study Research Investigators.
    Ethn Dis; 2006 Aug 01; 16(4):815-21. PubMed ID: 17061732
    [Abstract] [Full Text] [Related]

  • 3. Morbidity risk in HFE associated hereditary hemochromatosis C282Y heterozygotes.
    Fuchs J, Podda M, Packer L, Kaufmann R.
    Toxicology; 2002 Nov 15; 180(2):169-81. PubMed ID: 12324192
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  • 4. 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 15; 114(2):474-84. PubMed ID: 11529872
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 35(3):329-35. PubMed ID: 11887210
    [Abstract] [Full Text] [Related]

  • 6. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
    Brissot P, Moirand R, Jouanolle AM, Guyader D, Le Gall JY, Deugnier Y, David V.
    J Hepatol; 1999 Apr 15; 30(4):588-93. PubMed ID: 10207799
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  • 8. 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 Apr 15; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

  • 9. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R, Seidl C, Schilling S, Braner A, Seifried E, Hoelzer D, Kaltwasser JP.
    Eur J Immunogenet; 2000 Jun 15; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 10. Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands.
    Barton JC, Sawada-Hirai R, Rothenberg BE, Acton RT.
    Blood Cells Mol Dis; 1999 Jun 15; 25(3-4):147-55. PubMed ID: 10575540
    [Abstract] [Full Text] [Related]

  • 11. Transferrin receptor-2 (TFR2) mutation Y250X in Alabama Caucasian and African American subjects with and without primary iron overload.
    Barton EH, West PA, Rivers CA, Barton JC, Acton RT.
    Blood Cells Mol Dis; 2001 Jun 15; 27(1):279-84. PubMed ID: 11358388
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 23(2):314-20. PubMed ID: 9410475
    [Abstract] [Full Text] [Related]

  • 13. Evidence from a Ghanaian population of known African descent to support the proposition that hemochromatosis is a Caucasian disorder.
    Jeffery S, Crosby A, Plange-Rhule J, Amoah-Danquah J, Acheampong JW, Eastwood JB, Malik AK.
    Genet Test; 1999 Aug 15; 3(4):375-7. PubMed ID: 10627947
    [Abstract] [Full Text] [Related]

  • 14. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 15; 52(6):602-8. PubMed ID: 16871764
    [Abstract] [Full Text] [Related]

  • 15. 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 15; 41(11):1069-76. PubMed ID: 14648375
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. HFE gene mutations an Apulian population: allele frequencies.
    Pietrapertosa A, Vitucci A, Campanale D, Palma A, Renni R, Delios G, Tannoia N.
    Eur J Epidemiol; 2003 Nov 23; 18(7):685-9. PubMed ID: 12952143
    [Abstract] [Full Text] [Related]

  • 18. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L, Juzenas S, Sventoraityte J, Cedaviciute R, Vitkauskiene A, Kalibatas V, Kondrackiene J, Kupcinskas L.
    Ann Hematol; 2012 Apr 23; 91(4):491-5. PubMed ID: 21947086
    [Abstract] [Full Text] [Related]

  • 19. Prevalence of HFE gene C282Y and H63D mutations in a French-Canadian population of neonates and in referred patients.
    Girouard J, Giguère Y, Delage R, Rousseau F.
    Hum Mol Genet; 2002 Jan 15; 11(2):185-9. PubMed ID: 11809727
    [Abstract] [Full Text] [Related]

  • 20. C282Y and H63D mutations in the HFE gene have no effect on iron overload disorders in Japan.
    Shiono Y, Ikeda R, Hayashi H, Wakusawa S, Sanae F, Takikawa T, Imaizumi Y, Yano M, Yoshioka K, Kawanaka M, Yamada G.
    Intern Med; 2001 Sep 15; 40(9):852-6. PubMed ID: 11579943
    [Abstract] [Full Text] [Related]

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