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Journal Abstract Search

169 related items for PubMed ID: 14670915

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  • 3. 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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  • 4. 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 15; 46(4):302-7. PubMed ID: 21411349
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  • 5. 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 Apr 15; 33(3):338-43. PubMed ID: 15528154
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  • 7. Non-HFE hemochromatosis.
    Pietrangelo A.
    Semin Liver Dis; 2005 Nov 15; 25(4):450-60. PubMed ID: 16315138
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  • 9. HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
    Barton JC, Acton RT, Leiendecker-Foster C, Lovato L, Adams PC, McLaren GD, Eckfeldt JH, McLaren CE, Reboussin DM, Gordeuk VR, Speechley MR, Reiss JA, Press RD, Dawkins FW, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators.
    Genet Test; 2007 Nov 15; 11(3):269-75. PubMed ID: 17949288
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  • 11. [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 15; 36(9 Pt 2):1271-7. PubMed ID: 17521857
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  • 13. 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 15; 84(11):710-4. PubMed ID: 19787796
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  • 14. Hemojuvelin and hepcidin genes sequencing in Brazilian patients with primary iron overload.
    de Lima Santos PC, Pereira AC, Cançado RD, Schettert IT, Hirata RD, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Genet Test Mol Biomarkers; 2010 Dec 15; 14(6):803-6. PubMed ID: 21039223
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  • 17. Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.
    Bridle KR, Frazer DM, Wilkins SJ, Dixon JL, Purdie DM, Crawford DH, Subramaniam VN, Powell LW, Anderson GJ, Ramm GA.
    Lancet; 2003 Feb 22; 361(9358):669-73. PubMed ID: 12606179
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  • 18. Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes.
    Pietrangelo A, Caleffi A, Henrion J, Ferrara F, Corradini E, Kulaksiz H, Stremmel W, Andreone P, Garuti C.
    Gastroenterology; 2005 Feb 22; 128(2):470-9. PubMed ID: 15685557
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  • 20. HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis.
    Shukla P, Julka S, Bhatia E, Shah S, Nagral A, Aggarwal R.
    Natl Med J India; 2006 Feb 22; 19(1):20-3. PubMed ID: 16570681
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