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157 related items for PubMed ID: 11358388

  • 1. 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; 27(1):279-84. PubMed ID: 11358388
    [Abstract] [Full Text] [Related]

  • 2. 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; 27(1):290-3. PubMed ID: 11358390
    [Abstract] [Full Text] [Related]

  • 3. 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; 25(3-4):147-55. PubMed ID: 10575540
    [Abstract] [Full Text] [Related]

  • 4. Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama.
    Barton JC, Acton RT.
    Genet Test; 2000; 4(2):199-206. PubMed ID: 10953960
    [Abstract] [Full Text] [Related]

  • 5. Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency.
    Barton JC, Acton RT.
    Genet Med; 2001; 3(4):294-300. PubMed ID: 11478530
    [Abstract] [Full Text] [Related]

  • 6. Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.
    Lee PL, Halloran C, West C, Beutler E.
    Blood Cells Mol Dis; 2001; 27(1):285-9. PubMed ID: 11358389
    [Abstract] [Full Text] [Related]

  • 7. Allele frequencies of hemojuvelin gene (HJV) I222N and G320V missense mutations in white and African American subjects from the general Alabama population.
    Barton JC, Rivers CA, Niyongere S, Bohannon SB, Acton RT.
    BMC Med Genet; 2004 Dec 20; 5():29. PubMed ID: 15610558
    [Abstract] [Full Text] [Related]

  • 8. 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 20; 27(3):129-34. PubMed ID: 10940080
    [Abstract] [Full Text] [Related]

  • 9. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
    Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC.
    Clinics (Sao Paulo); 2009 Jun 20; 64(9):837-41. PubMed ID: 19759876
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload.
    De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C.
    Haematologica; 2003 Apr 01; 88(4):396-401. PubMed ID: 12681966
    [Abstract] [Full Text] [Related]

  • 12. Transferrin receptor 2 (TfR2) and HFE mutational analysis in non-C282Y iron overload: identification of a novel TfR2 mutation.
    Mattman A, Huntsman D, Lockitch G, Langlois S, Buskard N, Ralston D, Butterfield Y, Rodrigues P, Jones S, Porto G, Marra M, De Sousa M, Vatcher G.
    Blood; 2002 Aug 01; 100(3):1075-7. PubMed ID: 12130528
    [Abstract] [Full Text] [Related]

  • 13. Genotypic and phenotypic heterogeneity of African Americans with primary iron overload.
    Barton JC, Acton RT, Rivers CA, Bertoli LF, Gelbart T, West C, Beutler E.
    Blood Cells Mol Dis; 2003 Aug 01; 31(3):310-9. PubMed ID: 14636644
    [Abstract] [Full Text] [Related]

  • 14. HFE mutations in African-American women with non-insulin-dependent diabetes mellitus.
    Acton RT, Barton JC, Bell DS, Go RC, Roseman JM.
    Ethn Dis; 2001 Aug 01; 11(4):578-84. PubMed ID: 11763282
    [Abstract] [Full Text] [Related]

  • 15. HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France.
    Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou JJ.
    Br J Dermatol; 2001 Mar 01; 144(3):533-9. PubMed ID: 11260010
    [Abstract] [Full Text] [Related]

  • 16. The influence of hemochromatosis mutations on iron overload of thalassemia major.
    Longo F, Zecchina G, Sbaiz L, Fischer R, Piga A, Camaschella C.
    Haematologica; 1999 Sep 01; 84(9):799-803. PubMed ID: 10477452
    [Abstract] [Full Text] [Related]

  • 17. 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 Sep 01; 16(4):815-21. PubMed ID: 17061732
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 67(2):110-8. PubMed ID: 11722599
    [Abstract] [Full Text] [Related]

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