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Characterization of ferroptosis in murine models of hemochromatosis
Hepatology, 2017 Ferroptosis is a recently identified iron‐dependent form of nonapoptotic cell death implicated in brain, kidney, and heart pathology. However, the biological roles of iron and iron metabolism in ferroptosis remain poorly understood.
Hao Wang, Peng An, Enjun Xie
exaly +2 more sources
ACG Clinical Guideline: Hereditary Hemochromatosis
American Journal of Gastroenterology, 2019 Hereditary hemochromatosis (HH) is one of the most common genetic disorders among persons of northern European descent. There have been recent advances in the diagnosis, management, and treatment of HH.
Kris V Kowdley +2 more
exaly +2 more sources
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Cardiology in Review, 2023
Hemochromatosis is a genetic disorder characterized by excessive absorption and accumulation of iron in the body. It is one of the most common inherited disorders. The excess iron deposition can cause damage to various organs, including the liver, heart,
Shamim Ahmed +3 more
semanticscholar +1 more source
Hemochromatosis is a genetic disorder characterized by excessive absorption and accumulation of iron in the body. It is one of the most common inherited disorders. The excess iron deposition can cause damage to various organs, including the liver, heart,
Shamim Ahmed +3 more
semanticscholar +1 more source
Clinics in Liver Disease, 2000
The recent cloning of the hemochromatosis gene (HFE) and the demonstration that a single missense mutation is responsible for 90% or more of patients with the disease, have stimulated renewed interest in all aspects of this common disease. The molecular tests for identifying mutations in HFE provide improved means for diagnosis, family screening, and ...
Powell, Lawrie W., Yapp, Thomas R.
openaire +4 more sources
The recent cloning of the hemochromatosis gene (HFE) and the demonstration that a single missense mutation is responsible for 90% or more of patients with the disease, have stimulated renewed interest in all aspects of this common disease. The molecular tests for identifying mutations in HFE provide improved means for diagnosis, family screening, and ...
Powell, Lawrie W., Yapp, Thomas R.
openaire +4 more sources