Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
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) Recommendations for splenectomy in hereditary hemolytic anemias
Haematologica, Volume 103, issue 5 by Haematologica - Issuu
Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
Cancers | Free Full-Text | Advancing Treatment of Bone Metastases through Novel Translational Approaches Targeting the Bone Microenvironment
Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
Oxidants and Antioxidants in the Redox Biochemistry of Human Red Blood Cells | ACS Omega
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency | Haematologica
PDF) Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
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IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
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Haematologica 1999;84: supplement to no. 9 - Supplements ...
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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
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
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
