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Journal Abstract Search

322 related items for PubMed ID: 14757427

  • 21. [Genetic iron overloads and hepatic insulin-resistance iron overload syndrome: an update].
    Ruivard M.
    Rev Med Interne; 2009 Jan; 30(1):35-42. PubMed ID: 18584923
    [Abstract] [Full Text] [Related]

  • 22. Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease.
    Zoller H, McFarlane I, Theurl I, Stadlmann S, Nemeth E, Oxley D, Ganz T, Halsall DJ, Cox TM, Vogel W.
    Hepatology; 2005 Aug; 42(2):466-72. PubMed ID: 15986403
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  • 23. Rare types of genetic hemochromatosis.
    Camaschella C, Poggiali E.
    Acta Haematol; 2009 Aug; 122(2-3):140-5. PubMed ID: 19907151
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  • 25. Inherited disorders of iron metabolism.
    Födinger M, Sunder-Plassmann G.
    Kidney Int Suppl; 1999 Mar; 69():S22-34. PubMed ID: 10084283
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  • 27. The SLC40A1 R178Q mutation is a recurrent cause of hemochromatosis and is associated with a novel pathogenic mechanism.
    Ka C, Guellec J, Pepermans X, Kannengiesser C, Ged C, Wuyts W, Cassiman D, de Ledinghen V, Varet B, de Kerguenec C, Oudin C, Gourlaouen I, Lefebvre T, Férec C, Callebaut I, Le Gac G.
    Haematologica; 2018 Nov; 103(11):1796-1805. PubMed ID: 30002125
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  • 29. Impact of D181V and A69T on the function of ferroportin as an iron export pump and hepcidin receptor.
    Praschberger R, Schranz M, Griffiths WJ, Baumgartner N, Hermann M, Lomas DJ, Pietrangelo A, Cox TM, Vogel W, Zoller H.
    Biochim Biophys Acta; 2014 Sep; 1842(9):1406-12. PubMed ID: 24859227
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  • 30. Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations.
    Hetet G, Devaux I, Soufir N, Grandchamp B, Beaumont C.
    Blood; 2003 Sep 01; 102(5):1904-10. PubMed ID: 12730114
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  • 31. Role of ferritin and ferroportin genes in unexplained hyperferritinaemia.
    Cazzola M.
    Best Pract Res Clin Haematol; 2005 Jun 01; 18(2):251-63. PubMed ID: 15737888
    [Abstract] [Full Text] [Related]

  • 32. Inherited iron overload disorders.
    Piperno A, Pelucchi S, Mariani R.
    Transl Gastroenterol Hepatol; 2020 Jun 01; 5():25. PubMed ID: 32258529
    [Abstract] [Full Text] [Related]

  • 33. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers.
    Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R.
    Haematologica; 2002 Mar 01; 87(3):242-5. PubMed ID: 11869934
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  • 35. Inborn errors of metabolism: iron.
    Worwood M.
    Br Med Bull; 1999 Mar 01; 55(3):556-67. PubMed ID: 10746346
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  • 37. The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients.
    Politou M, Kalotychou V, Pissia M, Rombos Y, Sakellaropoulos N, Papanikolaou G.
    Haematologica; 2004 Apr 01; 89(4):490-2. PubMed ID: 15075083
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  • 40. Analysis of SLC40A1 gene at the mRNA level reveals rapidly the causative mutations in patients with hereditary hemochromatosis type IV.
    Speletas M, Kioumi A, Loules G, Hytiroglou P, Tsitouridis J, Christakis J, Germenis AE.
    Blood Cells Mol Dis; 2008 Apr 01; 40(3):353-9. PubMed ID: 17997113
    [Abstract] [Full Text] [Related]

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