Showing 1 - 6 results of 6 for search '"hereditary hemochromatosis"', query time: 0.04s Refine Results
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    HFE-Associated Hereditary Haemochromatosis by Emmeke J Eijkelkamp, Thomas R Yapp, Lawrie W Powell

    Published 2000-01-01
    “…Hereditary hemochromatosis is a common inherited disorder of the iron metabolism. …”
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    Hyperferritinemia at the patient with chronic hepatitis C by Ye. N. German, A. O. Buyeverov, M. V. Mayevskaya, Ch. S. Pavlov, V. T. Ivashkin, A. A. Levina

    Published 2009-02-01
    “…To represent the patient with chronic hepatitis C with severe hyperferritinemia and absence of dominant mutations of hereditary hemochromatosis gene.Clinical case data. Patient К., 38 years, despite of rapid virologic response at combined antiviral therapy by pegilated interferon α-2а and ribavirin, had persistently high activity of transaminases and initially high level of serum ferritin increase twice.Conclusion. …”
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    A Late Presentation of a Fatal Disease: Juvenile Hemochromatosis by Cynthia Cherfane, Pauline Lee, Leana Guerin, Kyle Brown

    Published 2013-01-01
    “…Juvenile hemochromatosis is a rare and severe form of hereditary hemochromatosis. We report the case of a 39-year-old female who presented with heart failure and cirrhosis from previously unrecognized juvenile hemochromatosis. …”
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    Cardiac Failure after Liver Transplantation Requiring a Biventricular Assist Device by Rita Jermyn, Eiei Soe, David D’Alessandro, Julia Shin, William Jakobleff, Daniel Schwartz, Milan Kinkhabwala, Paul J. Gaglio

    Published 2014-01-01
    “…Increased hepatic iron load in extrahepatic organs of cirrhotic patients with and without hereditary hemochromatosis portends a poorer long term prognosis after liver transplant. …”
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    ER Stress and Iron Homeostasis: A New Frontier for the UPR by Susana J. Oliveira, Maria de Sousa, Jorge P. Pinto

    Published 2011-01-01
    “…The C282Y mutation of HFE accounts for the majority of cases of the iron overload disease Hereditary Hemochromatosis (HH). The conformational changes introduced by this mutation impair the HFE association with β2-microglobulin (β2m) and the cell surface expression of the protein: with two major consequences. …”
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