Cystatin C levels in patients with β-thalassemia during deferasirox treatment

Author:

Papassotiriou Ioannis,Margeli Alexandra,Hantzi Eugenia,Delaporta Polyxeni,Sergounioti Athanassia,Goussetis Evgenios,Ladis Vassilios,Kattamis Antonis

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference21 articles.

1. Diagnostic accuracy of cystatin C compared to serum creatinine for the estimation of renal dysfunction in adults and children—a meta-analysis;Roos;Clin. Biochem.,2007

2. A phase 3 study of deferasirox (ICL670), a once-daily oral iron chelator, in patients with b-thalassemia;Cappellini;Blood,2006

3. Phase II clinical evaluation of deferasirox, a once-daily oral chelating agent, in pediatric patients with β-thalassemia major;Galanello;Haematologica,2006

4. Randomized phase II trial of deferasirox (Exjade®, ICL670), a once-daily, orally-administered iron chelator, in comparison to deferoxamine in thalassemia patients with transfusional iron overload;Piga;Haematologica,2006

5. Relative response of patients with myelodysplastic syndromes and other transfusion-dependent anaemias to deferasirox (ICL670): a 1-yr prospective study;Porter;Eur. J. Haematol.,2008

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