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84 related items for PubMed ID: 15503019

  • 1. Distribution of the C282Y and H63D polymorphisms in hereditary hemochromatosis patients from the French Basque Country.
    Bauduer F, Scribans C, Degioanni A, Renoux M, Dutour O.
    Ann Hematol; 2005 Feb; 84(2):99-102. PubMed ID: 15503019
    [Abstract] [Full Text] [Related]

  • 2. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients.
    Potekhina ES, Lavrov AV, Samokhodskaya LM, Efimenko AY, Balatskiy AV, Baev AA, Litvinova MM, Nikitina LA, Shipulin GA, Bochkov NP, Tkachuk VA, Bochkov VN.
    Blood Cells Mol Dis; 2005 Feb; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 3. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Feb; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 4. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis.
    Sherrington CA, Knuiman MW, Divitini ML, Bartholomew HC, Cullen DJ, Olynyk JK.
    J Gastroenterol Hepatol; 2006 Mar; 21(3):595-8. PubMed ID: 16638105
    [Abstract] [Full Text] [Related]

  • 5. C282Y/H63D hemochromatosis mutations and microevolution: Speculations concerning the Basque population.
    Bauduer F.
    Homo; 2017 Jan; 68(1):38-41. PubMed ID: 28034447
    [Abstract] [Full Text] [Related]

  • 6. Hereditary hemochromatosis genotypes and risk of ischemic stroke.
    Ellervik C, Tybjaerg-Hansen A, Appleyard M, Sillesen H, Boysen G, Nordestgaard BG.
    Neurology; 2007 Mar 27; 68(13):1025-31. PubMed ID: 17389307
    [Abstract] [Full Text] [Related]

  • 7. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.
    Pedersen P, Milman N.
    Ann Hematol; 2009 Aug 27; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

  • 8. Hemochromatosis-causing mutations C282Y and H63D are not risk factors for atherothrombotic cerebral infarction.
    Hruskovicová H, Milanez T, Kobal J, Potisk KP, Petrovic D, Peterlin B.
    Med Sci Monit; 2005 Jul 27; 11(7):BR248-52. PubMed ID: 15990686
    [Abstract] [Full Text] [Related]

  • 9. Hemochromatosis-associated gene mutations in patients with myelodysplastic syndromes with refractory anemia with ringed sideroblasts.
    Nearman ZP, Szpurka H, Serio B, Warshawksy I, Theil K, Lichtin A, Sekeres MA, Maciejewski JP.
    Am J Hematol; 2007 Dec 27; 82(12):1076-9. PubMed ID: 17654685
    [Abstract] [Full Text] [Related]

  • 10. Genetic hemochromatosis is a rare disease entity among French Basques: a center-based study from the general hospital of Basque County.
    Bauduer F, Scribans C, Renoux M, Borot N.
    Ann Hematol; 2001 Aug 27; 80(8):472-3. PubMed ID: 11563593
    [Abstract] [Full Text] [Related]

  • 11. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry.
    Kowdley KV, Brandhagen DJ, Gish RG, Bass NM, Weinstein J, Schilsky ML, Fontana RJ, McCashland T, Cotler SJ, Bacon BR, Keeffe EB, Gordon F, Polissar N, National Hemochromatosis Transplant Registry.
    Gastroenterology; 2005 Aug 27; 129(2):494-503. PubMed ID: 16083706
    [Abstract] [Full Text] [Related]

  • 12. Hereditary hemochromatosis and risk of ischemic heart disease: a prospective study and a case-control study.
    Ellervik C, Tybjaerg-Hansen A, Grande P, Appleyard M, Nordestgaard BG.
    Circulation; 2005 Jul 12; 112(2):185-93. PubMed ID: 15998685
    [Abstract] [Full Text] [Related]

  • 13. Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification.
    Robinson G, Narasimhan S, Weatherall M, Beasley R.
    J Gastroenterol Hepatol; 2007 Jun 12; 22(6):852-4. PubMed ID: 17565641
    [Abstract] [Full Text] [Related]

  • 14. Detection of the C282Y and H63D polymorphisms associated with hereditary hemochromatosis using the ABI 7500 fast real time PCR platform.
    Tafe LJ, Belloni DR, Tsongalis GJ.
    Diagn Mol Pathol; 2007 Jun 12; 16(2):112-5. PubMed ID: 17525682
    [Abstract] [Full Text] [Related]

  • 15. Investigation of genetic variants of genes of the hemochromatosis pathway and their role in breast cancer.
    Abraham BK, Justenhoven C, Pesch B, Harth V, Weirich G, Baisch C, Rabstein S, Ko YD, Brüning T, Fischer HP, Haas S, Brod S, Oberkanins C, Hamann U, Brauch H, GENICA Network.
    Cancer Epidemiol Biomarkers Prev; 2005 May 12; 14(5):1102-7. PubMed ID: 15894659
    [Abstract] [Full Text] [Related]

  • 16. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload?
    de Diego C, Opazo S, Murga MJ, Martínez-Castro P.
    Eur J Haematol; 2007 Jan 12; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 17. Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
    Koyama C, Wakusawa S, Hayashi H, Suzuki R, Yano M, Yoshioka K, Kozuru M, Takayamam Y, Okada T, Mabuchi H.
    Haematologica; 2005 Mar 12; 90(3):302-7. PubMed ID: 15749661
    [Abstract] [Full Text] [Related]

  • 18. Hemochromatosis gene mutations and distal adenomatous colorectal polyps.
    McGlynn KA, Sakoda LC, Hu Y, Schoen RE, Bresalier RS, Yeager M, Chanock S, Hayes RB, Buetow KH.
    Cancer Epidemiol Biomarkers Prev; 2005 Jan 12; 14(1):158-63. PubMed ID: 15668490
    [Abstract] [Full Text] [Related]

  • 19. HFE genotypes and dietary heme iron: no evidence of strong gene-nutrient interaction on serum ferritin concentrations in middle-aged women.
    van der A DL, Peeters PH, Grobbee DE, Roest M, Voorbij HA, van der Schouw YT.
    Nutr Metab Cardiovasc Dis; 2006 Jan 12; 16(1):60-8. PubMed ID: 16399493
    [Abstract] [Full Text] [Related]

  • 20. The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.
    Kallianpur AR, Hall LD, Yadav M, Byrne DW, Speroff T, Dittus RS, Haines JL, Christman BW, Summar ML.
    Bone Marrow Transplant; 2005 Jun 12; 35(12):1155-64. PubMed ID: 15834437
    [Abstract] [Full Text] [Related]

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