Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
Non-transfusion-dependent thalassemias. - Abstract - Europe PMC
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients
Anemie
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders
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Pharmaceuticals | Free Full-Text | Targeting the Hematopoietic Stem Cell Niche in β-Thalassemia and Sickle Cell Disease
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Haematologica, Volume 107, Issue 7 by Haematologica - Issuu
Role of Iron in the Molecular Pathogenesis of Diseases and Therapeutic Opportunities | ACS Chemical Biology
Vol. 103 No. 3 (2018): March, 2018 | Haematologica
Sociologia della scienza e della tecnologia - Carocci editore
PDF) Genetic modifiers of -thalassemia and clinical severity as assessed by age at first transfusion | F. Anni and Stefania Satta - Academia.edu
hhaem atologica - Haematologica - Supplements
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PDF) Altered Calcium and Red-ox homeostasis underline defective haematopoiesis in Fanconi Anemia
Anemia nel neonato: cause, sintomi e terapia | GravidanzaOnLine
Validation of Several Formulas to Differentiate Thalassemia from Iron Deficiency Anemia and Proposal of a Thalassemia–Iron Deficiency Discrimination (TID) Predictive Score | Siriraj Medical Journal
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
Non-transfusion-dependent thalassemias
Haematologica, Volume 108, Issue 1 by Haematologica - Issuu
Molecular analysis of Fanconi anemia: the
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Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertension
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