Deferasirox versus deferoxamine in managing iron overload in patients with Sickle Cell Anaemia: a systematic review and meta-analysis
Author:
Affiliation:
1. Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
2. Haematology Research Unit, King Fahad Medical Research Centre, King Abdulaziz University, Jeddah, Saudi Arabia
Abstract
Publisher
SAGE Publications
Subject
Biochemistry (medical),Cell Biology,Biochemistry,General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/03000605221143290
Reference26 articles.
1. Pulmonary Complications of Sickle Cell Disease
2. Sickle Cell Disease—Genetics, Pathophysiology, Clinical Presentation and Treatment
3. Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial
4. Two-Year Analysis of Efficacy and Safety of Deferasirox Treatment for Transfusional Iron Overload in Sickle Cell Anemia Patients
5. Variability of homozygous sickle cell disease: The role of alpha and beta globin chain variation and other factors
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1. Ultrasound targeted microbubble destruction assisted exosomal delivery of siHmox1 effectively inhibits doxorubicin-induced cardiomyocyte ferroptosis;Journal of Nanobiotechnology;2024-09-02
2. Comparison of Deferasirox and Desferrioxamine in Term of Mean Serum Ferritin Levels in Patients of β-Thalassemia Major with Iron Overload;Pakistan Journal of Health Sciences;2024-08-31
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