Blood Biomarkers in Idiopathic Pulmonary Fibrosis

PURPOSE: Idiopathic pulmonary fibrosis (IPF) is a progressive and lethal lung disease of unknown origin whose incidence has been increasing over the latest decade partly as a consequence of population ageing. New anti-fibrotic therapy including pirfenidone and nintedanib have now proven efficacy in...

Full description

Saved in:
Bibliographic Details
Published in:Lung
Main Authors: Guiot, Julien, Moermans, Catherine, Henket, Monique, Corhay, Jean-Louis, Louis, Renaud
Format: Artigo
Language:Inglês
Published: Springer US 2017
Subjects:
State of the Art Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5437192/
https://ncbi.nlm.nih.gov/pubmed/28353114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00408-017-9993-5
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items