Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia | Haematologica
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
Haematologica, Volume 106, Issue 11 by Haematologica - Issuu
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
Haematologica, Volume 105, Issue 7 by Haematologica - Issuu
PDF) Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis
Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis. - Abstract - Europe PMC
PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies
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
PDF) Genetic modifiers of -thalassemia and clinical severity as assessed by age at first transfusion | F. Anni and Stefania Satta - Academia.edu
Haematologica, Volume 106, Issue 9 by Haematologica - Issuu
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
PDF) Indices in differentiating iron deficiency anemia from thalassemia trait- a comparative study
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
Vol. 107 No. 1 (2022): January, 2022 | Haematologica
Logistic‐Nomogram model based on red blood cell parameters to differentiate thalassemia trait and iron deficiency anemia in southern region of Fujian Province, China - Xu - 2023 - Journal of Clinical Laboratory
Role of Iron in the Molecular Pathogenesis of Diseases and Therapeutic Opportunities | ACS Chemical Biology
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
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
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica
