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)

  • 41. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
    Njajou OT; Houwing-Duistermaat JJ; Osborne RH; Vaessen N; Vergeer J; Heeringa J; Pols HA; Hofman A; van Duijn CM
    Eur J Hum Genet; 2003 Mar; 11(3):225-31. PubMed ID: 12673276
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Hereditary hemochromatosis: detection of C282Y and H63D mutations in HFE gene by means of guthrie cards in population of Czech Republic.
    Cimburova M; Putova I; Provaznikova H; Horak J
    Genet Epidemiol; 2002 Oct; 23(3):260-3. PubMed ID: 12384978
    [TBL] [Abstract][Full Text] [Related]  

  • 43. HFE C282Y homozygosity is associated with lower total and low-density lipoprotein cholesterol: The hemochromatosis and iron overload screening study.
    Adams PC; Pankow JS; Barton JC; Acton RT; Leiendecker-Foster C; McLaren GD; Speechley M; Eckfeldt JH
    Circ Cardiovasc Genet; 2009 Feb; 2(1):34-7. PubMed ID: 20031565
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Hereditary and acquired iron overload].
    de Korwin JD
    Nephrol Ther; 2006 Nov; 2 Suppl 5():S304-12. PubMed ID: 17373275
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Phenotypic expression of a novel C282Y/R226G compound heterozygous state in HFE hemochromatosis: molecular dynamics and biochemical studies.
    Cézard C; Rabbind Singh A; Le Gac G; Gourlaouen I; Ferec C; Rochette J
    Blood Cells Mol Dis; 2014 Jan; 52(1):27-34. PubMed ID: 23953397
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
    Drastíková M; Beránek M; Hegerová J; Putzová D
    Cas Lek Cesk; 2012; 151(9):428-31. PubMed ID: 23102134
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Correlates of hepcidin and NTBI according to HFE status in patients referred to a liver centre.
    Ryan E; Ryan JD; Russell J; Coughlan B; Tjalsma H; Swinkels DW; Stewart S; Crowe JP
    Acta Haematol; 2015; 133(2):155-61. PubMed ID: 25277871
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A Chinese patient with non-HFE-linked iron overload.
    Kng C; Ng FH; Ng WF; Wong BC; Grosso LE; Brunt EM; Bacon BR
    J Clin Gastroenterol; 2001 Jul; 33(1):69-71. PubMed ID: 11418796
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients.
    Santos PC; Cançado RD; Pereira AC; Schettert IT; Soares RA; Pagliusi RA; Hirata RD; Hirata MH; Teixeira AC; Figueiredo MS; Chiattone CS; Krieger JE; Guerra-Shinohara EM
    Blood Cells Mol Dis; 2011 Apr; 46(4):302-7. PubMed ID: 21411349
    [TBL] [Abstract][Full Text] [Related]  

  • 50. 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]  

  • 51. Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathy.
    Hannuksela J; Leppilampi M; Peuhkurinen K; Kärkkäinen S; Saastamoinen E; Heliö T; Kaartinen M; Nieminen MS; Nieminen P; Parkkila S
    Eur J Heart Fail; 2005 Jan; 7(1):103-8. PubMed ID: 15642540
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygote.
    Barton JC; West C; Lee PL; Beutler E
    Clin Genet; 2004 Sep; 66(3):214-6. PubMed ID: 15324319
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. Association of porphyria cutanea tarda with hereditary hemochromatosis.
    Mehrany K; Drage LA; Brandhagen DJ; Pittelkow MR
    J Am Acad Dermatol; 2004 Aug; 51(2):205-11. PubMed ID: 15280838
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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; 42(1):17-24. PubMed ID: 15061375
    [TBL] [Abstract][Full Text] [Related]  

  • 56. The hepcidin gene promoter nc.-1010C > T; -582A > G haplotype modulates serum ferritin in individuals carrying the common H63D mutation in HFE gene.
    Silva B; Pita L; Gomes S; Gonçalves J; Faustino P
    Ann Hematol; 2014 Dec; 93(12):2063-6. PubMed ID: 25015054
    [TBL] [Abstract][Full Text] [Related]  

  • 57. The influence of hemochromatosis mutations on iron overload of thalassemia major.
    Longo F; Zecchina G; Sbaiz L; Fischer R; Piga A; Camaschella C
    Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [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; 164(39):4545-7. PubMed ID: 12380399
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl.
    Aguilar-Martinez P; Lok CY; Cunat S; Cadet E; Robson K; Rochette J
    Haematologica; 2007 Mar; 92(3):421-2. PubMed ID: 17339196
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The C282Y polymorphism of the hereditary hemochromatosis gene is associated with increased sex hormone-binding globulin and normal testosterone levels in men.
    Yeap BB; Beilin J; Shi Z; Knuiman MW; Olynyk JK; Chubb SA; Bruce DG; Milward EA
    J Endocrinol Invest; 2010 Sep; 33(8):544-8. PubMed ID: 20160468
    [TBL] [Abstract][Full Text] [Related]  

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