PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies | Gian Forni - Academia.edu
Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from 3 decades follow-up in a hig
Haematologica, Volume 106, Issue 2 by Haematologica - Issuu
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
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Vol. 106 No. 5 (2021): May, 2021 | Haematologica
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Haematologica, Volume 107, Issue 11 by Haematologica - Issuu
PDF) Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
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
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis. - Abstract - Europe PMC
Sotatercept, a novel transforming growth factor ß ligand trap, improves anemia in ß-thalassemia: a phase II, open-label, dose-
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
PDF) Association of anemia with health-related quality of life and survival: A large population-based cohort study