PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from 3 decades follow-up in a hig
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2 - Haematologica - Supplements
Ferrata Storti Foundation
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Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
Ferrata Storti Foundation
Haematologica, Volume 106, Issue 2 by Haematologica - Issuu
Haematologica
Anemie
PDF) Association of anemia with health-related quality of life and survival: A large population-based cohort study
PDF) A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease | Fabrizio Minichilli - Academia.edu
Non-transfusion-dependent thalassemias | Haematologica
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
PDF) Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase
Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Ferrata Storti Foundation
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
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
