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Journal Abstract Search

265 related items for PubMed ID: 15528154

  • 1. Identification of new mutations of hepcidin and hemojuvelin in patients with HFE C282Y allele.
    Biasiotto G, Roetto A, Daraio F, Polotti A, Gerardi GM, Girelli D, Cremonesi L, Arosio P, Camaschella C.
    Blood Cells Mol Dis; 2004; 33(3):338-43. PubMed ID: 15528154
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  • 2. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene.
    Altès A, Bach V, Ruiz A, Esteve A, Felez J, Remacha AF, Sardà MP, Baiget M.
    Ann Hematol; 2009 Oct; 88(10):951-5. PubMed ID: 19214511
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  • 3. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload.
    Biasiotto G, Belloli S, Ruggeri G, Zanella I, Gerardi G, Corrado M, Gobbi E, Albertini A, Arosio P.
    Clin Chem; 2003 Dec; 49(12):1981-8. PubMed ID: 14633868
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  • 4. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
    Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ.
    Hum Mol Genet; 2003 Sep 01; 12(17):2241-7. PubMed ID: 12915468
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  • 5. [Pathophysiology and genetics of classic HFE (type 1) hemochromatosis].
    Loréal O, Ropert M, Mosser A, Déhais V, Deugnier Y, David V, Brissot P, Jouanolle AM.
    Presse Med; 2007 Sep 01; 36(9 Pt 2):1271-7. PubMed ID: 17521857
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  • 7. 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 Sep 01; 8(3):263-7. PubMed ID: 15727249
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  • 10. Transferrin receptor-2 gene and non-C282Y homozygous patients with hemochromatosis.
    Aguilar-Martinez P, Esculié-Coste C, Bismuth M, Giansily-Blaizot M, Larrey D, Schved JF.
    Blood Cells Mol Dis; 2001 Sep 01; 27(1):290-3. PubMed ID: 11358390
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  • 15. 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 Sep 01; 114(4):982-7. PubMed ID: 21495455
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  • 16. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants.
    Barton JC, Lafreniere SA, Leiendecker-Foster C, Li H, Acton RT, Press RD, Eckfeldt JH.
    Am J Hematol; 2009 Nov 01; 84(11):710-4. PubMed ID: 19787796
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  • 17. A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote.
    Wallace DF, Dooley JS, Walker AP.
    Gastroenterology; 1999 Jun 01; 116(6):1409-12. PubMed ID: 10348824
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  • 20. 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 01; 23(2):314-20. PubMed ID: 9410475
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