Iron overload indices rise linearly with transfusion rate in patients with sickle cell disease.
about
Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson's, Huntington's, Alzheimer's, prions, bactericides, chemical toxicology and others as examplesEstimating tissue iron burden: current status and future prospects.Capturing PLMS and their variability in children with sickle cell disease: does ankle activity monitoring measure up to polysomnography?Partial manual exchange reduces iron accumulation during chronic red cell transfusions for sickle cell disease.Profound morphological changes in the erythrocytes and fibrin networks of patients with hemochromatosis or with hyperferritinemia, and their normalization by iron chelators and other agents.Trends in transfusion burden among long-term survivors of childhood hematological malignancies.Iron in sickle-cell disease: what have we learned over the years?Renal iron load in sickle cell disease is influenced by severity of haemolysis.Assessing cardiac and liver iron overload in chronically transfused patients with sickle cell disease.
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Iron overload indices rise linearly with transfusion rate in patients with sickle cell disease.
description
2010 nî lūn-bûn
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Iron overload indices rise lin ...... ents with sickle cell disease.
@en
Iron overload indices rise lin ...... ents with sickle cell disease.
@nl
type
label
Iron overload indices rise lin ...... ents with sickle cell disease.
@en
Iron overload indices rise lin ...... ents with sickle cell disease.
@nl
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Iron overload indices rise lin ...... ents with sickle cell disease.
@en
Iron overload indices rise lin ...... ents with sickle cell disease.
@nl
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Iron overload indices rise lin ...... ents with sickle cell disease.
@en
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Adlette Inati
John C Wood
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2980-1; author reply 2981-2
P356
10.1182/BLOOD-2009-09-243568
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P577
2010-04-01T00:00:00Z