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pro vyhledávání: '"Nader S Alanazi"'
Autor:
Ibrahim M Dighriri, Khawlah K Alrabghi, Dilveen M Sulaiman, Abdulrahman M Alruwaili, Nader S Alanazi, Al-maha A Al-Sadiq, Amal M Hadadi, Bushra Y Sahli, Basil A Qasem, Manal T Alotaibi, Taif T Asiri, Salman M Majrashi, Noura T Alotibia, Afnan T Alhamyani, Amjad A Alharbi
Publikováno v:
Cureus. 14(11)
β-thalassemia is characterized by the faulty generation of hemoglobin resulting in an elevated α/β globin ratio; this led to several patients needing red blood cell (RBC) transfusions for the rest of their lives. Luspatercept is an erythroid matur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::568286e56b15719527273ecdb093d46a
https://pubmed.ncbi.nlm.nih.gov/36540460
https://pubmed.ncbi.nlm.nih.gov/36540460
