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75 related items for PubMed ID: 21932715

  • 1. Presence of hemochromatosis-associated mutations in Hispanic patients with iron overload.
    Nieves-Santiago P, Cancel D, Canales D, Toro DH.
    P R Health Sci J; 2011 Sep; 30(3):135-8. PubMed ID: 21932715
    [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. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects.
    Cruz E, Melo G, Lacerda R, Almeida S, Porto G.
    Blood Cells Mol Dis; 2006 Aug; 37(1):33-9. PubMed ID: 16762569
    [Abstract] [Full Text] [Related]

  • 4. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation.
    Shaheen NJ, Bacon BR, Grimm IS.
    Hepatology; 1998 Aug; 28(2):526-9. PubMed ID: 9696020
    [Abstract] [Full Text] [Related]

  • 5. 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; 78(1):66-71. PubMed ID: 17042772
    [Abstract] [Full Text] [Related]

  • 6. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
    Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R.
    Haematologica; 2002 Mar; 87(3):242-5. PubMed ID: 11869934
    [Abstract] [Full Text] [Related]

  • 7. 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; 26(3):298-304. PubMed ID: 16584391
    [Abstract] [Full Text] [Related]

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

  • 9. Porphyria cutanea tarda in Brazilian patients: association with hemochromatosis C282Y mutation and hepatitis C virus infection.
    Martinelli AL, Zago MA, Roselino AM, Filho AB, Villanova MG, Secaf M, Tavella MH, Ramalho LN, Zucoloto S, Franco RF.
    Am J Gastroenterol; 2000 Dec; 95(12):3516-21. PubMed ID: 11151887
    [Abstract] [Full Text] [Related]

  • 10. 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; 93(5):293-302. PubMed ID: 11488107
    [Abstract] [Full Text] [Related]

  • 11. 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; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

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

  • 13. The role of transferrin saturation as a screening test for hereditary haemochromatosis in an Irish population seeking medical care.
    O'Hara R, Cavanagh N, Cassidy M, Cullina M.
    Ann Clin Biochem; 2003 Mar; 40(Pt 2):169-74. PubMed ID: 12662406
    [Abstract] [Full Text] [Related]

  • 14. Is there a threshold of hepatic iron concentration that leads to cirrhosis in C282Y hemochromatosis?
    Adams PC.
    Am J Gastroenterol; 2001 Feb; 96(2):567-9. PubMed ID: 11232708
    [Abstract] [Full Text] [Related]

  • 15. Prevalence of hemochromatosis in the Puerto Rico veteran population.
    Pérez R, Toro D, Fournier J, Villanueva A.
    P R Health Sci J; 2007 Jun; 26(2):147-50. PubMed ID: 17722428
    [Abstract] [Full Text] [Related]

  • 16. The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C.
    Kazemi-Shirazi L, Datz C, Maier-Dobersberger T, Kaserer K, Hackl F, Polli C, Steindl PE, Penner E, Ferenci P.
    Gastroenterology; 1999 Jan; 116(1):127-34. PubMed ID: 9869610
    [Abstract] [Full Text] [Related]

  • 17. Biochemical expression of heterozygous hereditary hemochromatosis.
    de Valk B, Witlox RS, van der Schouw YT, Marx JJ.
    Eur J Intern Med; 2000 Dec 20; 11(6):317-321. PubMed ID: 11113655
    [Abstract] [Full Text] [Related]

  • 18. Classification and diagnosis of iron overload.
    Piperno A.
    Haematologica; 1998 May 20; 83(5):447-55. PubMed ID: 9658731
    [Abstract] [Full Text] [Related]

  • 19. Phenotypic characteristics and diagnoses of patients referred to an iron overload clinic.
    Dever JB, Mallory MA, Mallory JE, Wallace D, Kowdley KV.
    Dig Dis Sci; 2010 Mar 20; 55(3):803-7. PubMed ID: 20033846
    [Abstract] [Full Text] [Related]

  • 20. High incidence of hemochromatosis gene mutations in the myelodysplastic syndrome: the Budapest Study on 50 patients.
    Várkonyi J, Tarkovács G, Karádi I, Andrikovics H, Varga F, Varga F, Demeter J, Tordai A.
    Acta Haematol; 2003 Mar 20; 109(2):64-7. PubMed ID: 12624489
    [Abstract] [Full Text] [Related]

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