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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) 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

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
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

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PDF) Association of UGT1A1 polymorphism with prevalence and age at onset of  cholelithiasis in sickle cell anemia | Jacques Elion - Academia.edu
PDF) Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia | Jacques Elion - Academia.edu

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

Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity  and transfusion dependency | Haematologica
Hepcidin levels in Diamond-Blackfan anemia reflect erythropoietic activity and transfusion dependency | Haematologica

Sotatercept, a novel transforming growth factor β ligand trap, improves  anemia in β-thalassemia: a phase II, open-label, dose-
Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-

IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome
IJMS | Free Full-Text | EnvIRONmental Aspects in Myelodysplastic Syndrome

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

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

Ferrata Storti Foundation
Ferrata Storti Foundation

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

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

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

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

Scimmia faccia con denti storti in look cartone animato' Maglietta Slim Fit  da donna | Spreadshirt
Scimmia faccia con denti storti in look cartone animato' Maglietta Slim Fit da donna | Spreadshirt

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

Anemie
Anemie

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

Ferrata Storti Foundation
Ferrata Storti Foundation

PDF) A new severity score index for phenotypic classification and  evaluation of responses to treatment in type I Gaucher disease | Fabrizio  Minichilli - Academia.edu
PDF) A new severity score index for phenotypic classification and evaluation of responses to treatment in type I Gaucher disease | Fabrizio Minichilli - Academia.edu

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

PDF) Italian Society of Hematology Practice Guidelines for the management  of iron overload in thalassemia major and related disorders
PDF) Italian Society of Hematology Practice Guidelines for the management of iron overload in thalassemia major and related disorders

2 - Haematologica - Supplements
2 - Haematologica - Supplements