Idiopathic Pulmonary Fibrosis (IPF): An Overview

Idiopathic pulmonary fibrosis (IPF) is an interstitial lung disease characterised by chronic, progressive scarring of the lungs and the pathological hallmark of usual interstitial pneumonia. Current paradigms suggest alveolar epithelial cell damage is a key initiating factor. Globally, incidence of...

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Detalles Bibliográficos
Autores principales: Barratt, Shaney L., Creamer, Andrew, Hayton, Conal, Chaudhuri, Nazia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111543/
https://www.ncbi.nlm.nih.gov/pubmed/30082599
http://dx.doi.org/10.3390/jcm7080201

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6111543/
https://www.ncbi.nlm.nih.gov/pubmed/30082599
http://dx.doi.org/10.3390/jcm7080201

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