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PUBMED FOR HANDHELDS

Journal Abstract Search


266 related items for PubMed ID: 10586619

  • 1. [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]

  • 2. Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsy.
    Bartolo C, McAndrew PE, Sosolik RC, Cawley KA, Balcerzak SP, Brandt JT, Prior TW.
    Arch Pathol Lab Med; 1998 Jul 07; 122(7):633-7. PubMed ID: 9674544
    [Abstract] [Full Text] [Related]

  • 3. 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 07; 9(6):445-51. PubMed ID: 11436126
    [Abstract] [Full Text] [Related]

  • 4. 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 Jun 07; 35(2):182-8. PubMed ID: 16055358
    [Abstract] [Full Text] [Related]

  • 5. Searching for hereditary hemochromatosis.
    Laudicina RJ.
    Clin Lab Sci; 2006 Jun 07; 19(3):174-83. PubMed ID: 16910235
    [Abstract] [Full Text] [Related]

  • 6. 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 07; 88(8):775-84. PubMed ID: 19159930
    [Abstract] [Full Text] [Related]

  • 7. 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 07; 22(6):852-4. PubMed ID: 17565641
    [Abstract] [Full Text] [Related]

  • 8. 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 07; 16(2):112-5. PubMed ID: 17525682
    [Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Genotype screening for hereditary hemochromatosis among voluntary blood donors in Hungary.
    Andrikovics H, Kalmár L, Bors A, Fandl B, Petri I, Kalász L, Tordai A.
    Blood Cells Mol Dis; 2001 Sep 10; 27(1):334-41. PubMed ID: 11358395
    [Abstract] [Full Text] [Related]

  • 11. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation.
    Shaheen NJ, Bacon BR, Grimm IS.
    Hepatology; 1998 Aug 10; 28(2):526-9. PubMed ID: 9696020
    [Abstract] [Full Text] [Related]

  • 12. [Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards].
    Zdárský E, Horák J, Stríteský J, Heirler F.
    Cas Lek Cesk; 1999 Aug 23; 138(16):497-9. PubMed ID: 10566227
    [Abstract] [Full Text] [Related]

  • 13. High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa.
    de Villiers JN, Hillerman R, de Jong G, Langenhoven E, Rossouw H, Marx MP, Kotze MJ.
    S Afr Med J; 1999 Mar 23; 89(3):279-82. PubMed ID: 10226674
    [Abstract] [Full Text] [Related]

  • 14. Association of HFE gene C282Y and H63D mutations with liver cirrhosis in the Lithuanian population.
    Juzėnas S, Kupčinskas J, Valantienė I, Šumskienė J, Petrenkienė V, Kondrackienė J, Kučinskas L, Kiudelis G, Skiecevičienė J, Kupčinskas L.
    Medicina (Kaunas); 2016 Mar 23; 52(5):269-275. PubMed ID: 27816425
    [Abstract] [Full Text] [Related]

  • 15. Population screening for hemochromatosis by PCR using sequence-specific primers.
    Guttridge MG, Carter K, Worwood M, Darke C.
    Genet Test; 2000 Mar 23; 4(2):111-4. PubMed ID: 10953948
    [Abstract] [Full Text] [Related]

  • 16. Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.
    Crawford DH, Jazwinska EC, Cullen LM, Powell LW.
    Gastroenterology; 1998 May 23; 114(5):1003-8. PubMed ID: 9558290
    [Abstract] [Full Text] [Related]

  • 17. Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany.
    Nielsen P, Carpinteiro S, Fischer R, Cabeda JM, Porto G, Gabbe EE.
    Br J Haematol; 1998 Dec 23; 103(3):842-5. PubMed ID: 9858243
    [Abstract] [Full Text] [Related]

  • 18. Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration.
    Zamboni P, Tognazzo S, Izzo M, Pancaldi F, Scapoli GL, Liboni A, Gemmati D.
    J Vasc Surg; 2005 Aug 23; 42(2):309-14. PubMed ID: 16102632
    [Abstract] [Full Text] [Related]

  • 19. A Simple RFLP-Based Method for HFE Gene Multiplex Amplification and Determination of Hereditary Hemochromatosis-Causing Mutation C282Y and H63D Variant with Highly Sensitive Determination of Contamination.
    Ogouma-Aworet L, Rabes JP, de Mazancourt P.
    Biomed Res Int; 2020 Aug 23; 2020():9396318. PubMed ID: 33457423
    [Abstract] [Full Text] [Related]

  • 20. Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis.
    Jowkar Z, Geramizadeh B, Shariat M.
    Hepat Mon; 2011 Nov 23; 11(11):887-9. PubMed ID: 22308152
    [Abstract] [Full Text] [Related]


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