PDF) Altered Calcium and Red-ox homeostasis underline defective haematopoiesis in Fanconi Anemia
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
Haematologica 1999;84: supplement to no. 9 - Supplements ...
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Haematologica, Volume 103, Issue 3 by Haematologica - Issuu
PDF) Normal and pathological erythropoiesis in adults: From gene regulation to targeted treatment concepts
Role of Iron in the Molecular Pathogenesis of Diseases and Therapeutic Opportunities | ACS Chemical Biology
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
S. (a) Spleen weight/ mouse weight ratio in wild-type (wt) and... | Download Scientific Diagram
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
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
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Vol. 103 No. 3 (2018): March, 2018 | Haematologica
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | R. Grosse - Academia.edu
PDF) Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study | 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
Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
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