Challenges in transfusion and the role of Thalidomide in E‐β‐Thalassemia—A case report
Author:
Affiliation:
1. Department of Clinical Haematology and BMT TATA Medical Center Kolkata India
2. Department of Transfusion Medicine TATA Medical Center Kolkata India
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.3141
Reference11 articles.
1. RBC alloimmunization and autoimmunization among transfusion-dependent Arab thalassemia patients
2. Dramatic erythroid response to low-dose thalidomide in two patients with transfusion independent thalassemia and severe post-transfusional alloimmune hemolysis
3. Induction of fetal hemoglobin synthesis by CRISPR/Cas9-mediated editing of the human β-globin locus
4. Optimal response to thalidomide in a patient with thalassaemia major resistant to conventional therapy;Masera N;Blood Transfus,2010
5. Evaluation of novel fetal hemoglobin inducer drugs in treatment of β‐hemoglobinopathy disorders;Fard AD;Int J Hematol Oncol Stem Cell Res,2013
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1. Factors Influencing the Efficacy and Safety of Thalidomide in the Treatment of Transfusion-Dependent Thalassaemia;Advances in Clinical Medicine;2023
2. Evaluation of the combination therapy of hydroxyurea and thalidomide in β-thalassemia;Blood Advances;2022-12-27
3. Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective;Pharmaceuticals;2022-06-16
4. Investigating the Efficacy and Safety of Thalidomide for Treating Patients With ß-Thalassemia: A Meta-Analysis;Frontiers in Pharmacology;2022-01-11
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