BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 29731342)

  • 1. Radiological features of crystal-induced arthropathy associated with hereditary hemochromatosis with homozygous C282Y mutation.
    García García M
    Reumatol Clin (Engl Ed); 2020; 16(2 Pt 1):122-124. PubMed ID: 29731342
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 27(1):290-3. PubMed ID: 11358390
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic Malignancy.
    Atkins JL; Pilling LC; Masoli JAH; Kuo CL; Shearman JD; Adams PC; Melzer D
    JAMA; 2020 Nov; 324(20):2048-2057. PubMed ID: 33231665
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Iron-overload-related disease in HFE hereditary hemochromatosis.
    Allen KJ; Gurrin LC; Constantine CC; Osborne NJ; Delatycki MB; Nicoll AJ; McLaren CE; Bahlo M; Nisselle AE; Vulpe CD; Anderson GJ; Southey MC; Giles GG; English DR; Hopper JL; Olynyk JK; Powell LW; Gertig DM
    N Engl J Med; 2008 Jan; 358(3):221-30. PubMed ID: 18199861
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HFE p.C282Y homozygosity predisposes to rapid serum ferritin rise after menopause: A genotype-stratified cohort study of hemochromatosis in Australian women.
    Warne CD; Zaloumis SG; Bertalli NA; Delatycki MB; Nicoll AJ; McLaren CE; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ; Gurrin LC;
    J Gastroenterol Hepatol; 2017 Apr; 32(4):797-802. PubMed ID: 27784128
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis.
    Hamdi-Rozé H; Beaumont-Epinette MP; Ben Ali Z; Le Lan C; Loustaud-Ratti V; Causse X; Loreal O; Deugnier Y; Brissot P; Jouanolle AM; Bardou-Jacquet E
    Am J Hematol; 2016 Dec; 91(12):1202-1205. PubMed ID: 27518069
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 114(5):1003-8. PubMed ID: 9558290
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hemochromatosis in Ireland and HFE.
    Ryan E; O'keane C; Crowe J
    Blood Cells Mol Dis; 1998 Dec; 24(4):428-32. PubMed ID: 9851896
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases.
    Sham RL; Ou CY; Cappuccio J; Braggins C; Dunnigan K; Phatak PD
    Blood Cells Mol Dis; 1997 Aug; 23(2):314-20. PubMed ID: 9410475
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report.
    Wickramasinghe W; Karunathilaka C; Jayasinghe S; Gooneratne L
    J Med Case Rep; 2020 Jul; 14(1):93. PubMed ID: 32641120
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hemochromatosis and iron-overload screening in a racially diverse population.
    Adams PC; Reboussin DM; Barton JC; McLaren CE; Eckfeldt JH; McLaren GD; Dawkins FW; Acton RT; Harris EL; Gordeuk VR; Leiendecker-Foster C; Speechley M; Snively BM; Holup JL; Thomson E; Sholinsky P;
    N Engl J Med; 2005 Apr; 352(17):1769-78. PubMed ID: 15858186
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hemochromatosis Mutations, Brain Iron Imaging, and Dementia in the UK Biobank Cohort.
    Atkins JL; Pilling LC; Heales CJ; Savage S; Kuo CL; Kuchel GA; Steffens DC; Melzer D
    J Alzheimers Dis; 2021; 79(3):1203-1211. PubMed ID: 33427739
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Increased capacity of lymphocytes from hereditary hemochromatosis patients homozygous for the C282Y HFE mutation to respond to the genotoxic effect of diepoxybutane.
    Porto B; Vieira R; Porto G
    Mutat Res; 2009 Feb; 673(1):37-42. PubMed ID: 19146986
    [TBL] [Abstract][Full Text] [Related]  

  • 14.  GNPAT variant (D519G) is not associated with an elevated serum ferritin or iron removed by phlebotomy in patients referred for C282Y-linked hemochromatosis.
    Levstik A; Stuart A; Adams PC
    Ann Hepatol; 2016 Nov-Dec 2016; 15(6):907-910. PubMed ID: 27740525
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haemochromatosis arthropathy - a conundrum of the Celtic curse.
    Kiely PD
    J R Coll Physicians Edinb; 2018 Sep; 48(3):233-238. PubMed ID: 30191911
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary hemochromatosis in north-eastern Romania.
    Voicu PM; Cojocariu C; Petrescu-Dănilă E; Stanciu C; Covic M; Rusu M; Trifan A
    Rev Med Chir Soc Med Nat Iasi; 2010; 114(4):982-7. PubMed ID: 21495455
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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; 130(31-32):1112-9. PubMed ID: 11008304
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria.
    Brissot P; Moirand R; Jouanolle AM; Guyader D; Le Gall JY; Deugnier Y; David V
    J Hepatol; 1999 Apr; 30(4):588-93. PubMed ID: 10207799
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary hemochromatosis: molecular diagnosis and effect of treatment].
    Szczeklik W; Dropiński J; Dziedzina S; Szułdrzyński K; Biesiada G; Mach T; Sanak M
    Pol Arch Med Wewn; 2004 May; 111(5):593-6. PubMed ID: 15508811
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary Hemochromatosis Associations with Frailty, Sarcopenia and Chronic Pain: Evidence from 200,975 Older UK Biobank Participants.
    Tamosauskaite J; Atkins JL; Pilling LC; Kuo CL; Kuchel GA; Ferrucci L; Melzer D
    J Gerontol A Biol Sci Med Sci; 2019 Feb; 74(3):337-342. PubMed ID: 30657865
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.