Prognosis and Follow-Up of Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF), a devastating progressive interstitial lung disease (ILD) with no known cause, is the most common and deadly of the idiopathic interstitial pneumonias. With a median survival of 3–5 years following diagnosis, IPF is characterized by a progressive decline in lung...

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Detalles Bibliográficos
Autores principales: Fernández Fabrellas, Estrella, Peris Sánchez, Ricardo, Sabater Abad, Cristina, Juan Samper, Gustavo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024649/
https://www.ncbi.nlm.nih.gov/pubmed/29904028
http://dx.doi.org/10.3390/medsci6020051

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024649/
https://www.ncbi.nlm.nih.gov/pubmed/29904028
http://dx.doi.org/10.3390/medsci6020051

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