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Autor:
Denise Clayton PhD, Jason Shafrin PhD, Glorian Yen PhD, MPH, Soyon Lee PharmD, Lincy Geevarghese MD, Yulin Shi MS, Luyang He MS, Ying Shen MS, Anem Waheed MD, MPH
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 30 (2024)
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hematologic disorder commonly treated with complement inhibitors such as eculizumab, ravulizumab, and pegcetacoplan. This study aims to describe treatment patterns, healthcare resource uti
Externí odkaz:
https://doaj.org/article/e226b6e07ae8464abd9cea30723dcbbf