Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
Oxidants and Antioxidants in the Redox Biochemistry of Human Red Blood Cells | ACS Omega
Haematologica, Volume 103, Issue 3 by Haematologica - Issuu
PDF) Normal and pathological erythropoiesis in adults: From gene regulation to targeted treatment concepts
Haematologica, Volume 104, Issue 1 by Haematologica - Issuu
Cancers | Free Full-Text | Advancing Treatment of Bone Metastases through Novel Translational Approaches Targeting the Bone Microenvironment
Haematologica, Volume 103, issue 5 by Haematologica - Issuu
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
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
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.
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
Ferrata Storti Foundation
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica
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) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology | U. Ramenghi - Academia.edu
PDF) Recommendations for splenectomy in hereditary hemolytic anemias
Ferrata Storti Foundation. No commercial use is allowed
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study | Haematologica
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
Ferrata Storti Foundation
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients