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pro vyhledávání: '"Trudy Sale"'
Publikováno v:
Advances in Hematology, Vol 2024 (2024)
Sickle cell disease (SCD) is a common genetic disorder with potentially serious sequelae that can be effectively treated with hydroxyurea. Despite its favorable benefit-risk profile, hydroxyurea uptake in patients with SCD is low. A pilot study was c
Externí odkaz:
https://doaj.org/article/1671a776a7144da19b925baa4a2d71b4
Publikováno v:
Blood. 138:1896-1896
Introduction: Sickle cell disease (SCD) is associated with major morbidity and mortality and yet many of our patients are not using the available disease modifying medication, hydroxyurea (HU). Furthermore, dose-titration of HU is required in order t