Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients | Haematologica
Haematologica, Volume 101, issue 2 by Haematologica - Issuu
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. - Abstract - Europe PMC
Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia | Haematologica
PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
PDF) Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency
PDF) Mosaic segmental uniparental isodisomy and progressive clonal selection: A common mechanism of late onset β-thalassemia major
Haematologica, Volume 106, Issue 9 by Haematologica - Issuu
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
PDF) Genetic modifiers of -thalassemia and clinical severity as assessed by age at first transfusion | F. Anni and Stefania Satta - Academia.edu
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica
Haematologica, Volume 106, Issue 1 by Haematologica - Issuu
Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Haematologica, Volume 104, Issue 1 by Haematologica - Issuu
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica
Hypercoagulability and thrombotic complications in hemolytic anemias | Haematologica
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. - Abstract - Europe PMC
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
Haematologica, Volume 104, Issue 3 by Haematologica - Issuu
