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
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Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
Non-transfusion-dependent thalassemias | Haematologica
Haematologica, Volume 107, Issue 11 by Haematologica - Issuu
PDF) A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease | Fabrizio Minichilli - Academia.edu
PDF) Association of anemia with health-related quality of life and survival: A large population-based cohort study
PDF) Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia | Jacques Elion - Academia.edu
Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis. - Abstract - Europe PMC
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
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
Vol. 106 No. 5 (2021): May, 2021 | Haematologica
Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from 3 decades follow-up in a hig
PDF) Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase
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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