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Autor:
Benjamin Seeliger, Alfonso Carleo, Pedro David Wendel-Garcia, Jan Fuge, Ana Montes-Warboys, Sven Schuchardt, Maria Molina-Molina, Antje Prasse
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Idiopathic pulmonary fibrosis (IPF) is a progressive disease with significant mortality and morbidity. Approval of antifibrotic therapy has ameliorated disease progression, but therapy response is heterogeneous and to date, adequate biomarkers predic
Externí odkaz:
https://doaj.org/article/5a2a3135693f43a8bba812aeeb763e89