Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
PDF) Altered Calcium and Red-ox homeostasis underline defective haematopoiesis in Fanconi Anemia
Haematologica, Volume 103, issue 5 by Haematologica - Issuu
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
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
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
Haematologica, Volume 104, Issue 1 by Haematologica - Issuu
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica
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Haematologica, Volume 106, Issue 9 by Haematologica - Issuu
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Haematologica, Volume 103, Issue 3 by Haematologica - Issuu
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study | Haematologica
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PDF) Recommendations for splenectomy in hereditary hemolytic anemias
Ferrata Storti Foundation
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | R. Grosse - Academia.edu
Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
Cancers | Free Full-Text | Advancing Treatment of Bone Metastases through Novel Translational Approaches Targeting the Bone Microenvironment
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.
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
