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PDF) 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
PDF) Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel
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IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
PDF) Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase
Ferrata Storti Foundation
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | M. Marchetti - Academia.edu
Haematologica, Volume 107, Issue 11 by Haematologica - Issuu
Validation of Several Formulas to Differentiate Thalassemia from Iron Deficiency Anemia and Proposal of a Thalassemia–Iron Deficiency Discrimination (TID) Predictive Score | Siriraj Medical Journal
PDF) Recommendations for splenectomy in hereditary hemolytic anemias
s3 - Supplements - Haematologica
Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Sotatercept, a novel transforming growth factor ß ligand trap, improves anemia in ß-thalassemia: a phase II, open-label, dose-
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Haematologica
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies | Gian Forni - Academia.edu