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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

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-

Ferrata Storti Foundation
Ferrata Storti Foundation

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

Haematologica
Haematologica

Untitled
Untitled

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

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

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

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

PDF) Association of anemia with health-related quality of life and  survival: A large population-based cohort study
PDF) Association of anemia with health-related quality of life and survival: A large population-based cohort study

PDF) Italian Society of Hematology practice guidelines for the management  of iron overload in thalassemia major and related disorders | M. Marchetti  - Academia.edu
PDF) Italian Society of Hematology practice guidelines for the management of iron overload in thalassemia major and related disorders | M. Marchetti - Academia.edu

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

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

PIEZO1 gain-of-function mutations delay reticulocyte maturation in  hereditary xerocytosis. - Abstract - Europe PMC
PIEZO1 gain-of-function mutations delay reticulocyte maturation in hereditary xerocytosis. - Abstract - Europe PMC

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

Ferrata Storti Foundation
Ferrata Storti Foundation

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

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

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

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

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

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