Haematologica, Volume 104, Issue 1 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
Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | R. Grosse - Academia.edu
PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
S. (a) Spleen weight/ mouse weight ratio in wild-type (wt) and... | Download Scientific Diagram
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica
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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 | U. Ramenghi - Academia.edu
Haematologica, Volume 103, Issue 3 by Haematologica - Issuu
PDF) Recommendations for splenectomy in hereditary hemolytic anemias
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
Haematologica, Volume 103, issue 5 by Haematologica - Issuu
Anemie
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
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
Haematologica 1999;84: supplement to no. 9 - Supplements ...
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