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 *

254 related articles for article (PubMed ID: 17483072)

  • 21. Screening for iron overload in the Turkish population.
    Barut G; Balci H; Bozdayi M; Hatemi I; Ozcelik D; Senturk H
    Dig Dis; 2003; 21(3):279-85. PubMed ID: 14571105
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Frequency of HFE H63D, S65C, and C282Y mutations in patients with iron overload and controls from Toledo, Spain.
    de Diego C; Murga MJ; Martínez-Castro P
    Genet Test; 2004; 8(3):263-7. PubMed ID: 15727249
    [TBL] [Abstract][Full Text] [Related]  

  • 24. HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes.
    Raddatz D; Legler T; Lynen R; Addicks N; Ramadori G
    Z Gastroenterol; 2003 Nov; 41(11):1069-76. PubMed ID: 14648375
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. The clinical relevance of compound heterozygosity for the C282Y and H63D substitutions in hemochromatosis.
    Walsh A; Dixon JL; Ramm GA; Hewett DG; Lincoln DJ; Anderson GJ; Subramaniam VN; Dodemaide J; Cavanaugh JA; Bassett ML; Powell LW
    Clin Gastroenterol Hepatol; 2006 Nov; 4(11):1403-10. PubMed ID: 16979952
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Prevalence of H63D, S65C, and C282Y hereditary hemochromatosis gene variants in Madeira Island (Portugal).
    Spínola C; Brehm A; Spínola H
    Ann Hematol; 2011 Jan; 90(1):29-32. PubMed ID: 20714725
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Abnormal regulation of HFE mRNA expression does not contribute to primary iron overload.
    Vercesi E; Cerani P; Rolandi V; Rovati A; Bergamaschi G
    Haematologica; 2000 Aug; 85(8):787-91. PubMed ID: 10942923
    [TBL] [Abstract][Full Text] [Related]  

  • 30. HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.
    Gurrin LC; Bertalli NA; Dalton GW; Osborne NJ; Constantine CC; McLaren CE; English DR; Gertig DM; Delatycki MB; Nicoll AJ; Southey MC; Hopper JL; Giles GG; Anderson GJ; Olynyk JK; Powell LW; Allen KJ;
    Hepatology; 2009 Jul; 50(1):94-101. PubMed ID: 19554541
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations of the HFE gene and the risk of hepatocellular carcinoma.
    Racchi O; Mangerini R; Rapezzi D; Gaetani GF; Nobile MT; Picciotto A; Ferraris AM
    Blood Cells Mol Dis; 1999; 25(5-6):350-3. PubMed ID: 10660482
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Frequency and spectrum of hemochromatosis mutations in Tunisia.
    Zorai A; Harteveld CL; Rachdi R; Dellagi K; Abbes S; Delbini P; Giordano PC
    Hematol J; 2003; 4(6):433-5. PubMed ID: 14671616
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Compound heterozygous C282Y/Q283P and Q283P/H63D mutations in haemochromatosis.
    van Gammeren A; de Baar E; Schrauwen L; van Wijngaarden P
    Br J Haematol; 2015 Nov; 171(4):650-1. PubMed ID: 25850353
    [No Abstract]   [Full Text] [Related]  

  • 35. Definition of C282Y mutation in a hereditary hemochromatosis family from Turkey.
    Yönal O; Hatirnaz O; Akyüz F; Köroğlu G; Ozbek U; Cefle K; Mungan Z
    Turk J Gastroenterol; 2007 Mar; 18(1):53-7. PubMed ID: 17450498
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hereditary hemochromatosis: the clinical significance of the S65C mutation.
    Asberg A; Thorstensen K; Hveem K; Bjerve KS
    Genet Test; 2002; 6(1):59-62. PubMed ID: 12180078
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Uncommon mutations and polymorphisms in the hemochromatosis gene.
    Pointon JJ; Wallace D; Merryweather-Clarke AT; Robson KJ
    Genet Test; 2000; 4(2):151-61. PubMed ID: 10953955
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions.
    Sharma V; Panigrahi I; Dutta P; Tyagi S; Choudhry VP; Saxena R
    Indian J Pathol Microbiol; 2007 Jan; 50(1):82-5. PubMed ID: 17474269
    [TBL] [Abstract][Full Text] [Related]  

  • 39. HFE gene mutations in patients with altered iron metabolism in Argentina.
    Rossetti MV; Méndez M; Afonso S; Gerez E; Batlle A; Muñoz A; Parera V
    Cell Mol Biol (Noisy-le-grand); 2009 Jul; 55(2):31-5. PubMed ID: 19656448
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Immunohistochemistry of the Hfe protein in patients with hereditary hemochromatosis, iron deficiency anemia, and normal controls.
    Byrnes V; Ryan E; O'Keane C; Crowe J
    Blood Cells Mol Dis; 2000 Feb; 26(1):2-8. PubMed ID: 10772870
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.