Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
PDF) Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency
An NMR Study of the Bortezomib Degradation under Clinical Use Conditions – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
Ferrata Storti Foundation
PDF) Recommendations for splenectomy in hereditary hemolytic anemias
Oxidants and Antioxidants in the Redox Biochemistry of Human Red Blood Cells | ACS Omega
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica
Haematologica, Volume 104, Issue 1 by Haematologica - Issuu
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | R. Grosse - Academia.edu
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
Role of Iron in the Molecular Pathogenesis of Diseases and Therapeutic Opportunities | ACS Chemical Biology
Cancers | Free Full-Text | Advancing Treatment of Bone Metastases through Novel Translational Approaches Targeting the Bone Microenvironment
Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica
PDF) Altered Calcium and Red-ox homeostasis underline defective haematopoiesis in Fanconi Anemia
S. (a) Spleen weight/ mouse weight ratio in wild-type (wt) and... | Download Scientific Diagram
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study | Haematologica
Ferrata Storti Foundation
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
Haematologica, Volume 103, Issue 3 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) 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