201 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]
