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 *

196 related articles for article (PubMed ID: 17924859)

  • 1. The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?
    Olsson KS; Ritter B; Hansson N
    Eur J Haematol; 2007 Nov; 79(5):429-34. PubMed ID: 17924859
    [TBL] [Abstract][Full Text] [Related]  

  • 2. HLA haplotype map of river valley populations with hemochromatosis traced through five centuries in Central Sweden.
    Olsson KS; Ritter B; Hansson N; Chowdhury RR
    Eur J Haematol; 2008 Jul; 81(1):36-46. PubMed ID: 18363869
    [TBL] [Abstract][Full Text] [Related]  

  • 3. HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload.
    Olsson KS; Ritter B; Raha-Chowdhury R
    Eur J Haematol; 2010 Feb; 84(2):145-53. PubMed ID: 19912313
    [TBL] [Abstract][Full Text] [Related]  

  • 4. HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload.
    Barton JC; Wiener HW; Acton RT; Go RC
    Blood Cells Mol Dis; 2005; 34(1):38-47. PubMed ID: 15607698
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload.
    Cruz E; Vieira J; Almeida S; Lacerda R; Gartner A; Cardoso CS; Alves H; Porto G
    BMC Med Genet; 2006 Mar; 7():16. PubMed ID: 16509978
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes.
    Schroeder HW; Zhu ZB; March RE; Campbell RD; Berney SM; Nedospasov SA; Turetskaya RL; Atkinson TP; Go RC; Cooper MD; Volanakis JE
    Mol Med; 1998 Feb; 4(2):72-86. PubMed ID: 9508785
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular genetic diagnostics and screening of hereditary hemochromatosis].
    Zlocha J; Kovács L; Pozgayová S; Kupcová V; Durínová S
    Vnitr Lek; 2006 Jun; 52(6):602-8. PubMed ID: 16871764
    [TBL] [Abstract][Full Text] [Related]  

  • 8. HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity.
    Barton JC; Barton JC; Acton RT
    Hereditas; 2022 Jun; 159(1):25. PubMed ID: 35659379
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping.
    Barton JC; Barton JC; Acton RT
    Eur J Haematol; 2010 Nov; 85(5):439-47. PubMed ID: 20722701
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population.
    Wrede CE; Hutzler S; Bollheimer LC; Buettner R; Hellerbrand C; Schöelmerich J; Palitzsch KD
    Isr Med Assoc J; 2004 Jan; 6(1):30-3. PubMed ID: 14740507
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda.
    Gonzalez-Hevilla M; de Salamanca RE; Morales P; Martínez-Laso J; Fontanellas A; Castro MJ; Rojo R; Moscoso J; Zamora J; Serrano-Vela JI; Arnaiz-Villena A
    J Gastroenterol Hepatol; 2005 Mar; 20(3):456-62. PubMed ID: 15740492
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden.
    Olsson KS; Konar J; Dufva IH; Ricksten A; Raha-Chowdhury R
    Eur J Haematol; 2011 Jan; 86(1):75-82. PubMed ID: 20946107
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Common variable immunodeficiency and IgG subclass deficiency in central Alabama hemochromatosis probands homozygous for HFE C282Y.
    Barton JC; Bertoli LF; Acton RT
    Blood Cells Mol Dis; 2003; 31(1):102-11. PubMed ID: 12850493
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas.
    Costa M; Cruz E; Barton JC; Thorstensen K; Morais S; da Silva BM; Pinto JP; Vieira CP; Vieira J; Acton RT; Porto G
    PLoS One; 2013; 8(11):e79990. PubMed ID: 24282517
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients.
    Piperno A; Arosio C; Fargion S; Roetto A; Nicoli C; Girelli D; Sbaiz L; Gasparini P; Boari G; Sampietro M; Camaschella C
    Hepatology; 1996 Jul; 24(1):43-6. PubMed ID: 8707280
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HLA-linked hemochromatosis alleles in sporadic porphyria cutanea tarda.
    Edwards CQ; Griffen LM; Goldgar DE; Skolnick MH; Kushner JP
    Gastroenterology; 1989 Oct; 97(4):972-81. PubMed ID: 2789160
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Common local founder effects for Wilson's disease and hereditary hemochromatosis; mutation studies of a large family.
    Olsson KS; Wålinder O; Kindmark A; Williams R
    Scand J Gastroenterol; 2012 Sep; 47(8-9):1014-20. PubMed ID: 22774841
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda.
    Roberts AG; Whatley SD; Nicklin S; Worwood M; Pointon JJ; Stone C; Elder GH
    Hepatology; 1997 Jan; 25(1):159-61. PubMed ID: 8985283
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.