ANALYSIS OF DL--TOCOPHEROL AS ANTIOXIDANT ON MALONDIALDEHYDE LEVEL IN PEDIATRIC PATIENTS WITH -THALASSEMIA MAJOR

Thalassemia is a hereditary form of anemia that affects the synthesis of hemoglobin. The management of therapy in patients with b-thalassemia major which patients should receive continuous blood transfusions and increased iron absorption from the digestive tract causes excess iron in the body. This...

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Bibliographic Details
Main Authors: Levana Rismayanti, Yulistiani Yulistiani, Mia Ratwita Andarsini, Mariyatul Qibtiyah
Format: Article
Language:English
Published: Universitas Airlangga 2017-08-01
Series:Folia Medica Indonesiana
Subjects:
MDA
ROS
Online Access:https://e-journal.unair.ac.id/FMI/article/view/5490