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Journal Abstract Search

111 related items for PubMed ID: 12117686

  • 1. Genetic testing for haemochromatosis in patients with chondrocalcinosis.
    Timms AE, Sathananthan R, Bradbury L, Athanasou NA, Wordsworth BP, Brown MA.
    Ann Rheum Dis; 2002 Aug; 61(8):745-7. PubMed ID: 12117686
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  • 2. Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?
    Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.
    J Med Genet; 2005 May; 42(5):390-5. PubMed ID: 15863667
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  • 3. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.
    Schweiz Med Wochenschr; 2000 Aug 08; 130(31-32):1112-9. PubMed ID: 11008304
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  • 4. High prevalence of non-HFE gene-associated haemochromatosis in patients from southern Italy.
    De Marco F, Liguori R, Giardina MG, D'Armiento M, Angelucci E, Lucariello A, Morante R, Cimino L, Galeota-Lanza A, Tarantino G, Ascione A, Budillon G, Vecchione R, Martinelli R, Matarazzo M, De Simone V.
    Clin Chem Lab Med; 2004 Jan 08; 42(1):17-24. PubMed ID: 15061375
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  • 5. The H63D variant in the HFE gene predisposes to arthralgia, chondrocalcinosis and osteoarthritis.
    Alizadeh BZ, Njajou OT, Hazes JM, Hofman A, Slagboom PE, Pols HA, van Duijn CM.
    Ann Rheum Dis; 2007 Nov 08; 66(11):1436-42. PubMed ID: 17284543
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  • 6. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S.
    Vnitr Lek; 2006 Jun 08; 52(6):602-8. PubMed ID: 16871764
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  • 7. Hereditary haemochromatosis mutation frequencies in the general population.
    Bradley LA, Johnson DD, Palomaki GE, Haddow JE, Robertson NH, Ferrie RM.
    J Med Screen; 1998 Jun 08; 5(1):34-6. PubMed ID: 9575458
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  • 9. 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 Jun 08; 27(1):290-3. PubMed ID: 11358390
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  • 11. HFE gene C282Y, H63D and S65C mutations frequency in the Transylvania region, Romania.
    Trifa AP, Popp RA, Militaru MS, Farcaş MF, Crişan TO, Gana I, Cucuianu A, Pop IV.
    J Gastrointestin Liver Dis; 2012 Jun 08; 21(2):177-80. PubMed ID: 22720307
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  • 15. HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank.
    Lucas MR, Atkins JL, Pilling LC, Shearman JD, Melzer D.
    BMJ Open; 2024 Mar 13; 14(3):e081926. PubMed ID: 38479735
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  • 17. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
    Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ.
    Hum Mol Genet; 2003 Sep 01; 12(17):2241-7. PubMed ID: 12915468
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  • 18. [Prevalence of hemochromatosis-associated mutations in the hemochromatosis gene in the Danish population].
    Larsen LE, Ellervik C, Appleyard M, Nordestgaard BG, Birgens H, Tybjaerg-Hansen A.
    Ugeskr Laeger; 2002 Sep 23; 164(39):4545-7. PubMed ID: 12380399
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  • 19. Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis.
    Lawless MW, White M, Mankan AK, O'Dwyer MJ, Norris S.
    Tissue Antigens; 2007 Oct 23; 70(4):294-300. PubMed ID: 17767550
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