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Journal Abstract Search

485 related items for PubMed ID: 17729390

  • 1. Non-HFE haemochromatosis.
    Wallace DF, Subramaniam VN.
    World J Gastroenterol; 2007 Sep 21; 13(35):4690-8. PubMed ID: 17729390
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  • 2. New insights into iron homeostasis through the study of non-HFE hereditary haemochromatosis.
    Roetto A, Camaschella C.
    Best Pract Res Clin Haematol; 2005 Jun 21; 18(2):235-50. PubMed ID: 15737887
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  • 5. Non-HFE hepatic iron overload.
    Pietrangelo A, Caleffi A, Corradini E.
    Semin Liver Dis; 2011 Aug 21; 31(3):302-18. PubMed ID: 21901660
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  • 6. HFE, hepcidin and ferroportin gene mutations are not present in Indian patients with primary haemochromatosis.
    Shukla P, Julka S, Bhatia E, Shah S, Nagral A, Aggarwal R.
    Natl Med J India; 2006 Aug 21; 19(1):20-3. PubMed ID: 16570681
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  • 7. The mechanisms of systemic iron homeostasis and etiology, diagnosis, and treatment of hereditary hemochromatosis.
    Kawabata H.
    Int J Hematol; 2018 Jan 21; 107(1):31-43. PubMed ID: 29134618
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  • 10. Genetic haemochromatosis: genes and mutations associated with iron loading.
    Camaschella C, Roetto A, De Gobbi M.
    Best Pract Res Clin Haematol; 2002 Jun 21; 15(2):261-76. PubMed ID: 12401307
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  • 11. Molecular pathogenesis of hereditary hemochromatosis.
    Liu J, Pu C, Lang L, Qiao L, Abdullahi MA, Jiang C.
    Histol Histopathol; 2016 Aug 21; 31(8):833-40. PubMed ID: 27031690
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  • 13. Hereditary iron overload: update on pathophysiology, diagnosis, and treatment.
    Franchini M.
    Am J Hematol; 2006 Mar 21; 81(3):202-9. PubMed ID: 16493621
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  • 15. Genetics, Genetic Testing, and Management of Hemochromatosis: 15 Years Since Hepcidin.
    Pietrangelo A.
    Gastroenterology; 2015 Oct 21; 149(5):1240-1251.e4. PubMed ID: 26164493
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  • 16. Relative contribution of iron genes, dysmetabolism and hepatitis C virus (HCV) in the pathogenesis of altered iron regulation in HCV chronic hepatitis.
    Valenti L, Pulixi EA, Arosio P, Cremonesi L, Biasiotto G, Dongiovanni P, Maggioni M, Fargion S, Fracanzani AL.
    Haematologica; 2007 Aug 21; 92(8):1037-42. PubMed ID: 17640859
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  • 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
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  • 19. Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.
    Merryweather-Clarke AT, Cadet E, Bomford A, Capron D, Viprakasit V, Miller A, McHugh PJ, Chapman RW, Pointon JJ, Wimhurst VL, Livesey KJ, Tanphaichitr V, Rochette J, Robson KJ.
    Hum Mol Genet; 2003 Sep 01; 12(17):2241-7. PubMed ID: 12915468
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  • 20. Defective release of Hepcidin not defective synthesis is the primary pathogenic mechanism in HFE-Haemochromatosis.
    Arnold J, Sangwaiya A, Bhatkal B, Arnold A.
    Med Hypotheses; 2008 Sep 01; 70(6):1197-200. PubMed ID: 18054440
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