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223 related items for PubMed ID: 17565641

  • 1. 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; 22(6):852-4. PubMed ID: 17565641
    [Abstract] [Full Text] [Related]

  • 2. 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; 129(2):494-503. PubMed ID: 16083706
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Liver iron deposits in hepatitis B patients: association with severity of liver disease but not with hemochromatosis gene mutations.
    Martinelli AL, Filho AB, Franco RF, Tavella MH, Ramalho LN, Zucoloto S, Rodrigues SS, Zago MA.
    J Gastroenterol Hepatol; 2004 Sep; 19(9):1036-41. PubMed ID: 15304122
    [Abstract] [Full Text] [Related]

  • 5. Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).
    Lamoril J, Andant C, Gouya L, Malonova E, Grandchamp B, Martásek P, Deybac JC, Puy H.
    Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):33-41. PubMed ID: 11929045
    [Abstract] [Full Text] [Related]

  • 6. [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis].
    Andrikovics H, Klein I, Kalmár L, Bors A, Jermendy G, Petri I, Kalász L, Váradi A, Tordai A.
    Orv Hetil; 1999 Nov 07; 140(45):2517-22. PubMed ID: 10586619
    [Abstract] [Full Text] [Related]

  • 7. [Are the hemochromatosis (HFE) gene mutation and hepatitis C virus (HCV) infection risk factors for porphyria cutanea tarda?].
    Nagy Z, Kószó F, Pár A, Nagy A, Horányi M, Morvay M, Dobozy A, Mózsik G.
    Orv Hetil; 2000 Sep 10; 141(37):2031-4. PubMed ID: 11037612
    [Abstract] [Full Text] [Related]

  • 8. 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 10; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

  • 9. 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 10; 11(7):BR248-52. PubMed ID: 15990686
    [Abstract] [Full Text] [Related]

  • 10. 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 Jul 10; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 11. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Jul 10; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 12. The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosis.
    Adams LA, Angulo P, Abraham SC, Torgerson H, Brandhagen D.
    Liver Int; 2006 Apr 10; 26(3):298-304. PubMed ID: 16584391
    [Abstract] [Full Text] [Related]

  • 13. Haemochromatosis gene mutations in a clustered Italian population: evidence of high prevalence in people of Celtic ancestry.
    Pozzato G, Zorat F, Nascimben F, Gregorutti M, Comar C, Baracetti S, Vatta S, Bevilacqua E, Belgrano A, Crovella S, Amoroso A.
    Eur J Hum Genet; 2001 Jun 10; 9(6):445-51. PubMed ID: 11436126
    [Abstract] [Full Text] [Related]

  • 14. [Significance and prevalence of the C282Y gene mutation of primary hemochromatosis in the pathogenesis of pophyria cutanea tarda].
    Malina L, Zd'árský E, Dandová S, Michalíková H, Cerná M, Cimburová M.
    Cas Lek Cesk; 2000 Nov 22; 139(23):728-30. PubMed ID: 11191743
    [Abstract] [Full Text] [Related]

  • 15. 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 22; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 16. Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment.
    Pietrangelo A.
    Gastroenterology; 2010 Aug 22; 139(2):393-408, 408.e1-2. PubMed ID: 20542038
    [Abstract] [Full Text] [Related]

  • 17. Prevalence of the C282Y mutation of the hemochromatosis gene in liver transplant recipients and donors.
    Alanen KW, Chakrabarti S, Rawlins JJ, Howson W, Jeffrey G, Adams PC.
    Hepatology; 1999 Sep 22; 30(3):665-9. PubMed ID: 10462372
    [Abstract] [Full Text] [Related]

  • 18. C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload.
    Jorquera F, Domínguez A, Díaz-Golpe V, Espinel J, Muñoz F, Herrera A, Fernández-Gundín MJ, Vivas S, Olcoz JL.
    Rev Esp Enferm Dig; 2001 May 22; 93(5):293-302. PubMed ID: 11488107
    [Abstract] [Full Text] [Related]

  • 19. Compound heterozygosity for haemochromatosis gene mutations and hepatic iron overload in allogeneic bone marrow transplant recipients.
    Grigg AP, Bhathal PS.
    Pathology; 2001 Feb 22; 33(1):44-9. PubMed ID: 11280607
    [Abstract] [Full Text] [Related]

  • 20. 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 22; 14(1):158-63. PubMed ID: 15668490
    [Abstract] [Full Text] [Related]

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