Exploring the Role of Biomarkers Associated with Alveolar Damage and Dysfunction in Idiopathic Pulmonary Fibrosis—A Systematic Review

Background: Idiopathic pulmonary fibrosis (IPF) is one of the most aggressive forms of interstitial lung diseases (ILDs), marked by an ongoing, chronic fibrotic process within the lung tissue. IPF leads to an irreversible deterioration of lung function, ultimately resulting in an increased mortality...

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Detalles Bibliográficos
Autores principales: Zamfir, Alexandra-Simona, Zabara, Mihai Lucian, Arcana, Raluca Ioana, Cernomaz, Tudor Andrei, Zabara-Antal, Andreea, Marcu, Marius Traian Dragoș, Trofor, Antigona, Zamfir, Carmen Lăcrămioara, Crișan-Dabija, Radu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10672103/
https://www.ncbi.nlm.nih.gov/pubmed/38003922
http://dx.doi.org/10.3390/jpm13111607

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