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Journal Abstract Search

237 related items for PubMed ID: 15290237

  • 1. The origin and spread of the HFE-C282Y haemochromatosis mutation.
    Distante S, Robson KJ, Graham-Campbell J, Arnaiz-Villena A, Brissot P, Worwood M.
    Hum Genet; 2004 Sep; 115(4):269-79. PubMed ID: 15290237
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  • 6. 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
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  • 11. Geography of HFE C282Y and H63D mutations.
    Merryweather-Clarke AT, Pointon JJ, Jouanolle AM, Rochette J, Robson KJ.
    Genet Test; 2000 Jan; 4(2):183-98. PubMed ID: 10953959
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  • 12. Haemochromatosis: pathological or beneficial.
    Worwood M.
    Schweiz Med Wochenschr; 1998 Dec 05; 128(49):1925-35. PubMed ID: 9887470
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  • 13. 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 05; 85(5):439-47. PubMed ID: 20722701
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  • 14. 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 05; 20(3):456-62. PubMed ID: 15740492
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  • 15. Prevalence of the C282Y mutation for haemochromatosis on the Island of Majorca.
    Guix P, Picornell A, Parera M, Tomás C, Muncunill J, Castro JA, Rossell J, Vaquer P, Ramon MM, Obrador A.
    Clin Genet; 2000 Aug 05; 58(2):123-8. PubMed ID: 11005145
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  • 16. 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 05; 42(1):17-24. PubMed ID: 15061375
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  • 17. 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 01; 84(2):145-53. PubMed ID: 19912313
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  • 18. Linkage disequilibrium between S65C HFE mutation and HLA A29-B44 haplotype in Terceira Island, Azores.
    Couto AR, Peixoto MJ, Garrett F, Laranjeira F, Cipriano T, Armas JB.
    Hum Immunol; 2003 Jun 01; 64(6):625-8. PubMed ID: 12770794
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  • 19. 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 01; 91(4):491-5. PubMed ID: 21947086
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  • 20. [Frequency of HFE gene mutations and genotype-phenotype correlations in patients with hereditary hemochromatosis in Switzerland].
    Himmelmann A, Bortoluzzi L, Jansen S, Fehr J.
    Schweiz Med Wochenschr; 2000 Aug 08; 130(31-32):1112-9. PubMed ID: 11008304
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