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PUBMED FOR HANDHELDS

Journal Abstract Search


286 related items for PubMed ID: 15701302

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  • 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
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  • 3. [Non-HFE-related hereditary iron overload].
    Aguilar-Martinez P.
    Presse Med; 2007 Sep 15; 36(9 Pt 2):1279-91. PubMed ID: 17540536
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  • 4. Non-HFE hemochromatosis.
    Pietrangelo A.
    Semin Liver Dis; 2005 Nov 15; 25(4):450-60. PubMed ID: 16315138
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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 15; 36(9 Pt 2):1271-7. PubMed ID: 17521857
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  • 10. Iron overload and prolonged ingestion of iron supplements: clinical features and mutation analysis of hemochromatosis-associated genes in four cases.
    Barton JC, Lee PL, West C, Bottomley SS.
    Am J Hematol; 2006 Oct 15; 81(10):760-7. PubMed ID: 16838333
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  • 16. Hereditary hemochromatosis: missed diagnosis or misdiagnosis?
    Cherfane CE, Hollenbeck RD, Go J, Brown KE.
    Am J Med; 2013 Nov 15; 126(11):1010-5. PubMed ID: 24054178
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  • 17. Rare types of genetic hemochromatosis.
    Camaschella C, Poggiali E.
    Acta Haematol; 2009 Nov 15; 122(2-3):140-5. PubMed ID: 19907151
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  • 19. Differing impact of the deletion of hemochromatosis-associated molecules HFE and transferrin receptor-2 on the iron phenotype of mice lacking bone morphogenetic protein 6 or hemojuvelin.
    Latour C, Besson-Fournier C, Meynard D, Silvestri L, Gourbeyre O, Aguilar-Martinez P, Schmidt PJ, Fleming MD, Roth MP, Coppin H.
    Hepatology; 2016 Jan 15; 63(1):126-37. PubMed ID: 26406355
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  • 20. Hereditary hemochromatosis: pathogenesis, diagnosis, and treatment.
    Pietrangelo A.
    Gastroenterology; 2010 Aug 15; 139(2):393-408, 408.e1-2. PubMed ID: 20542038
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