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Autor:
Abigél Margit Kolonics-Farkas, Martina Šterclová, Nesrin Mogulkoc, Katarzyna Lewandowska, Veronika Müller, Marta Hájková, Mordechai Kramer, Dragana Jovanovic, Jasna Tekavec-Trkanjec, Michael Studnicka, Natalia Stoeva, Simona Littnerová, Martina Vašáková
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Idiopathic pulmonary fibrosis (IPF) is a rare lung disease with poor prognosis. The diagnosis and treatment possibilities are dependent on the health systems of countries. Hence, comparison among countries is difficult due to data heterogeneity. Our
Externí odkaz:
https://doaj.org/article/b399851ef6f24b1fa825cc97e6b8ce39