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775 related items for PubMed ID: 16315138

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

  • 2. [Non-HFE-related hereditary iron overload].
    Aguilar-Martinez P.
    Presse Med; 2007 Sep; 36(9 Pt 2):1279-91. PubMed ID: 17540536
    [Abstract] [Full Text] [Related]

  • 3. [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; 36(9 Pt 2):1271-7. PubMed ID: 17521857
    [Abstract] [Full Text] [Related]

  • 4. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.
    Franchini M.
    Am J Hematol; 2006 Mar; 81(3):202-9. PubMed ID: 16493621
    [Abstract] [Full Text] [Related]

  • 5. [Hypersiderosis and dissiderosis in the context of data on hemochromatosis microelementosis].
    Smirnov OA.
    Arkh Patol; 2008 Mar; 70(3):3-8. PubMed ID: 18727423
    [Abstract] [Full Text] [Related]

  • 6. New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis.
    Roetto A, Camaschella C.
    Best Pract Res Clin Haematol; 2005 Jun; 18(2):235-50. PubMed ID: 15737887
    [Abstract] [Full Text] [Related]

  • 7. Non-HFE haemochromatosis.
    Wallace DF, Subramaniam VN.
    World J Gastroenterol; 2007 Sep 21; 13(35):4690-8. PubMed ID: 17729390
    [Abstract] [Full Text] [Related]

  • 8. Non-HFE hepatic iron overload.
    Pietrangelo A, Caleffi A, Corradini E.
    Semin Liver Dis; 2011 Aug 21; 31(3):302-18. PubMed ID: 21901660
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload.
    Biasiotto G, Belloli S, Ruggeri G, Zanella I, Gerardi G, Corrado M, Gobbi E, Albertini A, Arosio P.
    Clin Chem; 2003 Dec 15; 49(12):1981-8. PubMed ID: 14633868
    [Abstract] [Full Text] [Related]

  • 11. The molecular pathogenesis of hereditary hemochromatosis.
    Babitt JL, Lin HY.
    Semin Liver Dis; 2011 Aug 15; 31(3):280-92. PubMed ID: 21901658
    [Abstract] [Full Text] [Related]

  • 12. 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 Aug 15; 38(1):37-44. PubMed ID: 17098454
    [Abstract] [Full Text] [Related]

  • 13. Constitutive hepcidin expression prevents iron overload in a mouse model of hemochromatosis.
    Nicolas G, Viatte L, Lou DQ, Bennoun M, Beaumont C, Kahn A, Andrews NC, Vaulont S.
    Nat Genet; 2003 May 15; 34(1):97-101. PubMed ID: 12704388
    [Abstract] [Full Text] [Related]

  • 14. Hemochromatosis: genetics and pathophysiology.
    Beutler E.
    Annu Rev Med; 2006 May 15; 57():331-47. PubMed ID: 16409153
    [Abstract] [Full Text] [Related]

  • 15. Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice.
    Delima RD, Chua AC, Tirnitz-Parker JE, Gan EK, Croft KD, Graham RM, Olynyk JK, Trinder D.
    Hepatology; 2012 Aug 15; 56(2):585-93. PubMed ID: 22383097
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Function of the hemochromatosis protein HFE: Lessons from animal models.
    Pantopoulos K.
    World J Gastroenterol; 2008 Dec 07; 14(45):6893-901. PubMed ID: 19058322
    [Abstract] [Full Text] [Related]

  • 20. Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
    Del-Castillo-Rueda A, Moreno-Carralero MI, Cuadrado-Grande N, Alvarez-Sala-Walther LA, Enríquez-de-Salamanca R, Méndez M, Morán-Jiménez MJ.
    Gene; 2012 Oct 15; 508(1):15-20. PubMed ID: 22890139
    [Abstract] [Full Text] [Related]

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