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pro vyhledávání: '"Abdulrahman Raiza"'
Autor:
Giamal Gmati, Moussab Damlaj, Tahani Alanazy, Maybelle Balili, Heba Alshobaki, Walid Mashaqbeh, Husam Mazin Alsadi, Abdulrahman Raiza, Mohsen Alzahrani, Hind Salama, Ayman Hejazi, Muhammad Qureshi, Khadega A. Abuelgasim, Mazin Ahmed, Bader Alahmari, Ahmed Alaskar, Abdulrahman Alghamdi
Publikováno v:
Blood. 136:1-2
Background: Allogeneic HSCT for adult patients with sickle cell disease (SCD) is potentially curative but not commonly utilized therapy due to complications such as graft failure (GF) and organ toxicity. At our center, we adopted a non-myeloablative