Hydroxyurea treatment in transfusion-dependent β-thalassemia patients

β-Thalassemia is an inherited hemoglobin disorder caused by defective synthesis of ß-globin chains. Hemoglobin (Hb) F induction is a possible therapeutic approach which can partially compensate for α and non-α globin chains imbalance. Objectives : We aimed to investigate the efficacy and safety of H...

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Veröffentlicht in:	Iranian red crescent medical journal 2014-06, Vol.16 (6), p.1-6
Hauptverfasser:	Karimi, Mahran, Bardestani, Mardih, Kamfiroozi, Ruza, Haghpanah, Suzan, Bordbar, Muhammad Rida, Silavizadeh, Samir
Format:	Artikel
Sprache:	eng
Schlagworte:	Blood tests Hydroxyurea Thalassemia Therapeutic use Treatment Variance analysis الثلاسيميا
Online-Zugang:	Volltext
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