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Daily alternating deferasirox and deferiprone therapy successfully controls iron accumulation in untreatable transfusion-dependent thalassemia patients.

Valeria Maria PintoManuela BaloccoSabrina QuintinoLorenzo BacigalupoBarbara GianesinMonica RizziRoberto MalagòLucia De FranceschiGian Luca Forni
Published in: American journal of hematology (2018)
Keyphrases
  • ejection fraction
  • newly diagnosed
  • physical activity
  • sickle cell disease
  • stem cells
  • bone marrow
  • cell therapy