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Study of T lymphocyte Subsets in children with Beta Thalassemia Major: Correlation with iron overload Adel A. Hagag, Mokhtar A. Hussein, Enaam S. Abed Elbar* From Pediatrics and Clinical Pathology*departments, Faculty of Medicine, Tanta University, Egy

Abstract: Beta thalassemia is an inherited hemoglobin disorder resulting in chronic hemolytic anemia that typically requires life long transfusion therapy. Repeated blood transfusions and RBCs hemolysis are the major causes of secondary iron overload which is one of the predisposing factors to infe...

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Glavni avtor: adel abd elhaleim hagag
Format: Artigo
Jezik:Inglês
Izdano: PAGEPress Publications 2014-08-01
Serija:Mediterranean Journal of Hematology and Infectious Diseases
Teme:
Online dostop:https://mjhid.org/index.php/mjhid/article/view/1778
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