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PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
PDF) Mosaic segmental uniparental isodisomy and progressive clonal selection: A common mechanism of late onset β-thalassemia major
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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PDF) A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease | Fabrizio Minichilli - Academia.edu
Haematologica
Sotatercept, a novel transforming growth factor ß ligand trap, improves anemia in ß-thalassemia: a phase II, open-label, dose-
Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Haematologica, Volume 107, Issue 11 by Haematologica - Issuu
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
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Haematologica, Volume 105, 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) 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) Recommendations for splenectomy in hereditary hemolytic anemias
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis. - Abstract - Europe PMC
Vol. 104 No. 3 (2019): March, 2019 | Haematologica
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
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
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
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