Hydroxyurea Treatment in Transfusion-Dependent β-Thalassemia Patients

BACKGROUND: 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...

Full description

Saved in:
Bibliographic Details
Main Authors: Bordbar, Mohammad Reza, Silavizadeh, Samir, Haghpanah, Sezaneh, Kamfiroozi, Roza, Bardestani, Marzieh, Karimi, Mehran
Format: Artigo
Language:Inglês
Published: Kowsar 2014
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4102988/
https://ncbi.nlm.nih.gov/pubmed/25068055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/ircmj.18028
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items