PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | R. Grosse - Academia.edu
Cancers | Free Full-Text | Advancing Treatment of Bone Metastases through Novel Translational Approaches Targeting the Bone Microenvironment
PDF) Normal and pathological erythropoiesis in adults: From gene regulation to targeted treatment concepts
Haematologica, Volume 103, issue 5 by Haematologica - Issuu
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PDF) Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia
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) Recommendations for splenectomy in hereditary hemolytic anemias
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort | Haematologica
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Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | 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
Haematologica, Volume 106, Issue 9 by Haematologica - Issuu
Role of Iron in the Molecular Pathogenesis of Diseases and Therapeutic Opportunities | ACS Chemical Biology
Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica
PDF) Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology
Congenital sideroblastic anemia associated with germline polymorphisms reducing expression of FECH | Haematologica
Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major
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Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
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Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
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) Altered Calcium and Red-ox homeostasis underline defective haematopoiesis in Fanconi Anemia
Hematologic responses in patients with aplastic anemia treated with deferasirox: a post hoc analysis from the EPIC study | Haematologica
