Iron Metabolism in Thalassemia and Sickle Cell Disease.

There are two main mechanisms by which iron overload develops in thalassemias: increased iron absorption due to ineffective erythropoiesis and blood transfusions. In nontransfused patients with severe thalassemia, abnormal dietary iron absorption increases body iron burden between 2 and 5 g per year...

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Bibliografische gegevens
Hoofdauteurs: Mariani, Raffaella, Trombini, Paola, Pozzi, Matteo, Piperno, Alberto
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Università Cattolica del Sacro Cuore 2009
Onderwerpen:
Review Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3033158/
https://ncbi.nlm.nih.gov/pubmed/21415988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4084/MJHID.2009.006
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