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PUBMED FOR HANDHELDS

Journal Abstract Search

108 related items for PubMed ID: 12850485

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  • 2. Association between the HFE mutations and unsuccessful ageing: a study in Alzheimer's disease patients from Northern Italy.
    Candore G, Licastro F, Chiappelli M, Franceschi C, Lio D, Rita Balistreri C, Piazza G, Colonna-Romano G, Grimaldi LM, Caruso C.
    Mech Ageing Dev; 2003 Apr; 124(4):525-8. PubMed ID: 12714262
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  • 4. Risk factors for development of dementia in a unique six-year cohort study. I. An exploratory, pilot study of involvement of the E4 allele of apolipoprotein E, mutations of the hemochromatosis-HFE gene, type 2 diabetes, and stroke.
    Percy M, Somerville MJ, Hicks M, Garcia A, Colelli T, Wright E, Kitaygorodsky J, Jiang A, Ho V, Parpia A, Wong MK.
    J Alzheimers Dis; 2014 Apr; 38(4):907-22. PubMed ID: 24081379
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  • 6. 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; 91(4):491-5. PubMed ID: 21947086
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  • 7. Mutations of the hemochromatosis gene in Italian candidate blood donors with increased transferrin saturation.
    Velati C, Marlianici E, Rigamonti D, Barillari G, Chiavilli F, Fugiani P, Garozzo G, Lancieri M, Rinaldi S, Testa D, Sampietro M, Tavazzi D, Delbini P, Fargion S, Fiorelli G.
    Hematol J; 2003 Apr; 4(6):436-40. PubMed ID: 14671617
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  • 8. Analysis of HFE gene mutations (C282Y, H63D, and S65C) in the Ecuadorian population.
    Leone PE, Giménez P, Collantes JC, Paz-y-Miño C.
    Ann Hematol; 2005 Feb; 84(2):103-5. PubMed ID: 15517265
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  • 13. 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; 42(1):17-24. PubMed ID: 15061375
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  • 14. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City.
    Baptista-González HA, Rosenfeld-Mann F, Trueba-Gómez R, Bermejo-Martínez L, Méndez-Sánchez N.
    Ann Hepatol; 2007 Jan; 6(1):55-60. PubMed ID: 17297430
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  • 16. [The importance of DNA analysis of C282Y, H63D and S65C mutations in the HFE gene].
    Drastíková M, Beránek M, Hegerová J, Putzová D.
    Cas Lek Cesk; 2012 Jan; 151(9):428-31. PubMed ID: 23102134
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  • 17. Prevalence and penetrance of HFE mutations in 4865 unselected primary care patients.
    Phatak PD, Ryan DH, Cappuccio J, Oakes D, Braggins C, Provenzano K, Eberly S, Sham RL.
    Blood Cells Mol Dis; 2002 Jan; 29(1):41-7. PubMed ID: 12482402
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  • 19. A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.
    Njajou OT, Houwing-Duistermaat JJ, Osborne RH, Vaessen N, Vergeer J, Heeringa J, Pols HA, Hofman A, van Duijn CM.
    Eur J Hum Genet; 2003 Mar; 11(3):225-31. PubMed ID: 12673276
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  • 20. HFE genotype, parenchymal iron accumulation, and liver fibrosis in patients with nonalcoholic fatty liver disease.
    Valenti L, Fracanzani AL, Bugianesi E, Dongiovanni P, Galmozzi E, Vanni E, Canavesi E, Lattuada E, Roviaro G, Marchesini G, Fargion S.
    Gastroenterology; 2010 Mar; 138(3):905-12. PubMed ID: 19931264
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