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PDF) Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel
PDF) Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: Indications and management recommendations from an international expert panel

Haematologica, Volume 106, Issue 2 by Haematologica - Issuu
Haematologica, Volume 106, Issue 2 by Haematologica - Issuu

Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica
Circulating microparticles in children with sickle cell anemia: a heterogeneous procoagulant storm directed by hemolysis and fetal hemoglobin | Haematologica

Anemie
Anemie

Ferrata Storti Foundation
Ferrata Storti Foundation

Ferrata Storti Foundation
Ferrata Storti Foundation

Haematologica, Volume 105, issue 2 by Haematologica - Issuu
Haematologica, Volume 105, issue 2 by Haematologica - Issuu

Haematologica
Haematologica

Ferrata Storti Foundation
Ferrata Storti Foundation

Haematologica, Volume 105, Issue 11 by Haematologica - Issuu
Haematologica, Volume 105, Issue 11 by Haematologica - Issuu

Vol. 106 No. 5 (2021): May, 2021 | Haematologica
Vol. 106 No. 5 (2021): May, 2021 | Haematologica

Non-transfusion-dependent thalassemias | Haematologica
Non-transfusion-dependent thalassemias | Haematologica

Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients
Diagnostics | Free Full-Text | The TVGH-NYCU Thal-Classifier: Development of a Machine-Learning Classifier for Differentiating Thalassemia and Non-Thalassemia Patients

PDF) Mosaic segmental uniparental isodisomy and progressive clonal selection: A common mechanism of late onset β-thalassemia major
PDF) Mosaic segmental uniparental isodisomy and progressive clonal selection: A common mechanism of late onset β-thalassemia major

Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from 3 decades follow-up in a hig
Morbidity and mortality of sickle cell disease patients is unaffected by splenectomy: evidence from 3 decades follow-up in a hig

Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC
Evaluation of the diagnostic reliability of Mentzer index for Beta thalassemia trait followed by HPLC

s3 - Supplements - Haematologica
s3 - Supplements - Haematologica

Impaired bone marrow microenvironment and stem cells in transfusion-dependent beta-thalassemia - ScienceDirect
Impaired bone marrow microenvironment and stem cells in transfusion-dependent beta-thalassemia - ScienceDirect

PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies | Gian Forni - Academia.edu
PDF) Efficacy and safety of sildenafil in the treatment of severe pulmonary hypertension in patients with hemoglobinopathies | Gian Forni - Academia.edu

PDF) Recommendations for splenectomy in hereditary hemolytic anemias
PDF) Recommendations for splenectomy in hereditary hemolytic anemias

Vol. 104 No. 3 (2019): March, 2019 | Haematologica
Vol. 104 No. 3 (2019): March, 2019 | Haematologica

PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice
PDF) Resveratrol accelerates erythroid maturation by activation of FOXO3 and ameliorates anemia in beta-thalassemic mice

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) 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) Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase
PDF) Thalassemic erythrocytes release microparticles loaded with hemichromes by redox activation of p72Syk kinase

2 - Haematologica - Supplements
2 - Haematologica - Supplements

PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu
PDF) Elevated liver iron concentration is a marker of increased morbidity in patients with thalassemia intermedia | Hani Tamim - Academia.edu