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Journal Abstract Search

208 related items for PubMed ID: 23577916

  • 1. Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutations.
    McDonald CJ, Wallace DF, Crawford DH, Subramaniam VN.
    J Gastroenterol Hepatol; 2013 Jul; 28(7):1087-94. PubMed ID: 23577916
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Hereditary hemochromatosis in a Brazilian university hospital in São Paulo State (1990-2000).
    Martinelli AL, Filho R, Cruz S, Franco R, Tavella M, Secaf M, Ramalho L, Zucoloto S, Rodrigues S, Zago M.
    Genet Mol Res; 2005 Mar 31; 4(1):31-8. PubMed ID: 15841433
    [Abstract] [Full Text] [Related]

  • 4. Hepatic iron metabolism gene expression profiles in HFE associated hereditary hemochromatosis.
    Gleeson F, Ryan E, Barrett S, Russell J, Crowe J.
    Blood Cells Mol Dis; 2007 Mar 31; 38(1):37-44. PubMed ID: 17098454
    [Abstract] [Full Text] [Related]

  • 5. Identification of novel mutations in hemochromatosis genes by targeted next generation sequencing in Italian patients with unexplained iron overload.
    Badar S, Busti F, Ferrarini A, Xumerle L, Bozzini P, Capelli P, Pozzi-Mucelli R, Campostrini N, De Matteis G, Marin Vargas S, Giorgetti A, Delledonne M, Olivieri O, Girelli D.
    Am J Hematol; 2016 Jun 31; 91(4):420-5. PubMed ID: 26799139
    [Abstract] [Full Text] [Related]

  • 6. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
    Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G.
    Ann Hematol; 2005 Oct 31; 84(10):646-9. PubMed ID: 15871018
    [Abstract] [Full Text] [Related]

  • 7. Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological data.
    Scotet V, Le Gac G, Mérour MC, Mercier AY, Chanu B, Ka C, Mura C, Nousbaum JB, Férec C.
    BMC Med Genet; 2005 Jun 01; 6():24. PubMed ID: 15929798
    [Abstract] [Full Text] [Related]

  • 8. Hereditary hemochromatosis.
    Fix OK, Kowdley KV.
    Minerva Med; 2008 Dec 01; 99(6):605-17. PubMed ID: 19034258
    [Abstract] [Full Text] [Related]

  • 9. Hereditary hemochromatosis in Spain.
    Sánchez M, Bruguera M, Quintero E, Barrio Y, Mazzara R, Rodés J, Oliva R.
    Genet Test; 2000 Dec 01; 4(2):171-6. PubMed ID: 10953957
    [Abstract] [Full Text] [Related]

  • 10. Geography of HFE C282Y and H63D mutations.
    Merryweather-Clarke AT, Pointon JJ, Jouanolle AM, Rochette J, Robson KJ.
    Genet Test; 2000 Dec 01; 4(2):183-98. PubMed ID: 10953959
    [Abstract] [Full Text] [Related]

  • 11. HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?
    Santos PC, Pereira AC, Cançado RD, Schettert IT, Sobreira TJ, Oliveira PS, Hirata RD, Hirata MH, Figueiredo MS, Chiattone CS, Krieger JE, Guerra-Shinohara EM.
    Blood Cells Mol Dis; 2010 Dec 15; 45(4):302-7. PubMed ID: 20843714
    [Abstract] [Full Text] [Related]

  • 12. HFE and non-HFE hemochromatosis.
    Anderson GJ, Powell LW.
    Int J Hematol; 2002 Oct 15; 76(3):203-7. PubMed ID: 12416729
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 88(10):951-5. PubMed ID: 19214511
    [Abstract] [Full Text] [Related]

  • 14. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.
    de Tayrac M, Roth MP, Jouanolle AM, Coppin H, le Gac G, Piperno A, Férec C, Pelucchi S, Scotet V, Bardou-Jacquet E, Ropert M, Bouvet R, Génin E, Mosser J, Deugnier Y.
    J Hepatol; 2015 Mar 15; 62(3):664-72. PubMed ID: 25457201
    [Abstract] [Full Text] [Related]

  • 15. Pathogenesis of hereditary hemochromatosis: genetics and beyond.
    Britton RS, Fleming RE, Parkkila S, Waheed A, Sly WS, Bacon BR.
    Semin Gastrointest Dis; 2002 Apr 15; 13(2):68-79. PubMed ID: 12064862
    [Abstract] [Full Text] [Related]

  • 16. Non-HFE hemochromatosis.
    Pietrangelo A.
    Semin Liver Dis; 2005 Nov 15; 25(4):450-60. PubMed ID: 16315138
    [Abstract] [Full Text] [Related]

  • 17. 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 Nov 15; 8(3):263-7. PubMed ID: 15727249
    [Abstract] [Full Text] [Related]

  • 18. 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 15; 91(4):491-5. PubMed ID: 21947086
    [Abstract] [Full Text] [Related]

  • 19. Hereditary hemochromatosis: awareness and genetic testing acceptability in Western Romania.
    Neghina AM, Anghel A.
    Genet Test Mol Biomarkers; 2010 Dec 15; 14(6):847-50. PubMed ID: 20979574
    [Abstract] [Full Text] [Related]

  • 20. EASL clinical practice guidelines for HFE hemochromatosis.
    European Association For The Study Of The Livereasl@easloffice.eu.
    J Hepatol; 2010 Jul 15; 53(1):3-22. PubMed ID: 20471131
    [Abstract] [Full Text] [Related]

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