Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia-Reference-Cited by-同舟云学术

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Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia

Published:2007-10 Issue:10 Volume:47 Page:1830-1836
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Bradai Mohamed,Pissard Serge,Abad Mohand Tayeb,Dechartres Agnes,Ribeil Jean-Antoine,Landais Paul,de Montalembert Mariane

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2007.01399.x/fullpdf

Reference28 articles.

1. Iron-Chelating Therapy and the Treatment of Thalassemia

2. β-Thalassemia

3. Effect of Hydroxyurea on the Frequency of Painful Crises in Sickle Cell Anemia

4. Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease

5. Successful Use of Hydroxyurea in β-Thalassemia Major

Cited by 57 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Thalidomide and Hydroxyurea in Transfusion-Dependent Thalassemia: Efficacy, Safety Profile and Impact on Quality of Life;Hemoglobin;2024-08-02

2. Foetal haemoglobin inducers for reducing blood transfusion in non-transfusion-dependent beta-thalassaemias;Cochrane Database of Systematic Reviews;2023-01-13

3. IVS I-5 (G > C) is associated with changes to the RBC membrane lipidome in response to hydroxyurea treatment in β-thalassemia patients;Molecular Omics;2022

4. Drug Repurposing: Hydroxyurea Therapy Improves the Transfusion-Free Interval in HbE/Beta-Thalassemia—Major Patients with the XmnI Polymorphism;Genetic Testing and Molecular Biomarkers;2021-08-01

5. Oral ferroportin inhibitor vamifeport for improving iron homeostasis and erythropoiesis in β-thalassemia: current evidence and future clinical development;Expert Review of Hematology;2021-07-03

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