These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 19433916)

  • 1. Mutant HFE genotype leads to significant iron overload in patients with liver diseases from western Romania.
    Neghina AM; Anghel A; Sporea I; Popescu A; Neghina R; Collins A; Thorstensen K
    J Appl Genet; 2009; 50(2):173-6. PubMed ID: 19433916
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls.
    Holmström P; Marmur J; Eggertsen G; Gåfvels M; Stål P
    Gut; 2002 Nov; 51(5):723-30. PubMed ID: 12377814
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Mutations in the HFE gene (C282Y, H63D, S65C) in alcoholic patients with finding of iron overload].
    Campos Franco J; González Quintela A; Fernández de Trocóniz LL; Barros Angueira F; Pérez-Quintela BV; Pérez Becerra E; Martínez de Rituerto ST; Otero Antón E; Torre Carballada JA
    Rev Clin Esp; 2002 Oct; 202(10):534-9. PubMed ID: 12361551
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effects of C282Y, H63D, and S65C HFE gene mutations, diet, and life-style factors on iron status in a general Mediterranean population from Tarragona, Spain.
    Aranda N; Viteri FE; Montserrat C; Arija V
    Ann Hematol; 2010 Aug; 89(8):767-73. PubMed ID: 20107990
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload.
    Cançado RD; Guglielmi AC; Vergueiro CS; Rolim EG; Figueiredo MS; Chiattone CS
    Sao Paulo Med J; 2006 Mar; 124(2):55-60. PubMed ID: 16878186
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frequency of the S65C mutation of HFE and iron overload in 309 subjects heterozygous for C282Y.
    Wallace DF; Walker AP; Pietrangelo A; Clare M; Bomford AB; Dixon JL; Powell LW; Subramaniam VN; Dooley JS
    J Hepatol; 2002 Apr; 36(4):474-9. PubMed ID: 11943417
    [TBL] [Abstract][Full Text] [Related]  

  • 7. HFE mutations, iron deficiency and overload in 10,500 blood donors.
    Jackson HA; Carter K; Darke C; Guttridge MG; Ravine D; Hutton RD; Napier JA; Worwood M
    Br J Haematol; 2001 Aug; 114(2):474-84. PubMed ID: 11529872
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 21(2):177-80. PubMed ID: 22720307
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prevalence of H63D, S65C and C282Y hereditary hemochromatosis gene mutations in Slovenian population by an improved high-throughput genotyping assay.
    Cukjati M; Vaupotic T; Rupreht R; Curin-Serbec V
    BMC Med Genet; 2007 Nov; 8():69. PubMed ID: 18036208
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload.
    Porto G; Cardoso CS; Gordeuk V; Cruz E; Fraga J; Areias J; Oliveira JC; Bravo F; Gangaidzo IT; MacPhail AP; Gomo ZA; Moyo VM; Melo G; Silva C; Justiça B; de Sousa M
    Eur J Haematol; 2001 Aug; 67(2):110-8. PubMed ID: 11722599
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy.
    Floreani A; Rosa Rizzotto E; Basso D; Navaglia F; Zaninotto M; Petridis I; DI Andrea O; Testa R; Marra M; Baldo V; Chiaramonte M
    Aliment Pharmacol Ther; 2007 Aug; 26(4):577-86. PubMed ID: 17661761
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City.
    Baptista-González HA; Rosenfeld-Mann F; Trueba-Gómez R; Bermejo-Martínez L; Méndez-Sánchez N
    Ann Hepatol; 2007; 6(1):55-60. PubMed ID: 17297430
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Iron-overload and genotypic expression of HFE mutations H63D/C282Y and transferrin receptor Hin6I and BanI polymorphism in german patients with hereditary haemochromatosis.
    Gottschalk R; Seidl C; Schilling S; Braner A; Seifried E; Hoelzer D; Kaltwasser JP
    Eur J Immunogenet; 2000 Jun; 27(3):129-34. PubMed ID: 10940080
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population.
    Kucinskas L; Juzenas S; Sventoraityte J; Cedaviciute R; Vitkauskiene A; Kalibatas V; Kondrackiene J; Kupcinskas L
    Ann Hematol; 2012 Apr; 91(4):491-5. PubMed ID: 21947086
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. HFE genotyping in patients with elevated serum iron indices and liver diseases.
    Evangelista AS; Nakhle MC; de Araújo TF; Abrantes-Lemos CP; Deguti MM; Carrilho FJ; Cançado EL
    Biomed Res Int; 2015; 2015():164671. PubMed ID: 25654085
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia].
    Nie L; Ai XF; Zheng YZ; Li QH; Yang L; Xiao ZJ
    Zhonghua Xue Ye Xue Za Zhi; 2009 Apr; 30(4):223-8. PubMed ID: 19731820
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HFE genotype in patients with hemochromatosis and other liver diseases.
    Bacon BR; Olynyk JK; Brunt EM; Britton RS; Wolff RK
    Ann Intern Med; 1999 Jun; 130(12):953-62. PubMed ID: 10383365
    [TBL] [Abstract][Full Text] [Related]  

  • 19. HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping.
    Koefoed P; Dalhoff K; Dissing J; Kramer I; Milman N; Pedersen P; Simonsen K; Tygstrup N; Nielsen FC
    Scand J Clin Lab Invest; 2002; 62(7):527-35. PubMed ID: 12512743
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Natural history of HFE simple heterozygosity for C282Y and H63D: a prospective 12-year study.
    Zaloumis SG; Allen KJ; Bertalli NA; Turkovic L; Delatycki MB; Nicoll AJ; McLaren CE; English DR; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Gurrin LC;
    J Gastroenterol Hepatol; 2015 Apr; 30(4):719-25. PubMed ID: 25311314
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.