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
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PDF) Normal and pathological erythropoiesis in adults: From gene regulation to targeted treatment concepts
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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
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
Haematologica, Volume 104, Issue 1 by Haematologica - Issuu
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Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
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PDF) Comparative analysis of oral and intravenous iron therapy in rat models of inflammatory anemia and iron deficiency
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PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
Haematologica 1999;84: supplement to no. 9 - Supplements ...
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
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PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study | Haematologica
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
