Vol. 106 No. 5 (2021): May, 2021 | Haematologica
Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-
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Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
Haematologica
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | M. Marchetti - Academia.edu
PDF) Mosaic segmental uniparental isodisomy and progressive clonal selection: A common mechanism of late onset β-thalassemia major
Haematologica, Volume 106, Issue 2 by Haematologica - Issuu
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PDF) Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase
PDF) A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease | Fabrizio Minichilli - Academia.edu
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) Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel
Impaired bone marrow microenvironment and stem cells in transfusion-dependent beta-thalassemia - ScienceDirect
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PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
Non-transfusion-dependent thalassemias | Haematologica
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PDF) Recommendations for splenectomy in hereditary hemolytic anemias
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
Sotatercept, a novel transforming growth factor ß ligand trap, improves anemia in ß-thalassemia: a phase II, open-label, dose-
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
