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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...

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Detalhes bibliográficos
Publicado no:Lung
Main Authors: Guiot, Julien, Moermans, Catherine, Henket, Monique, Corhay, Jean-Louis, Louis, Renaud
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2017
Assuntos:
Acesso em linha: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
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