IPF - Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis or IPF is a long-term (chronic) lung disease. IPF is part of a large group of diseases that cause scarring of the lungs (this is called fibrosis). The diseases that cause scarring of the lungs are called interstitial lung diseases (ILD).

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2019
Materias:
ELF factsheet
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544798/
https://www.ncbi.nlm.nih.gov/pubmed/31191732
http://dx.doi.org/10.1183/20734735.ELF152
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description Idiopathic pulmonary fibrosis or IPF is a long-term (chronic) lung disease. IPF is part of a large group of diseases that cause scarring of the lungs (this is called fibrosis). The diseases that cause scarring of the lungs are called interstitial lung diseases (ILD).
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spelling pubmed-65447982019-06-12 IPF - Idiopathic Pulmonary Fibrosis Breathe (Sheff) ELF factsheet Idiopathic pulmonary fibrosis or IPF is a long-term (chronic) lung disease. IPF is part of a large group of diseases that cause scarring of the lungs (this is called fibrosis). The diseases that cause scarring of the lungs are called interstitial lung diseases (ILD). European Respiratory Society 2019-06 /pmc/articles/PMC6544798/ /pubmed/31191732 http://dx.doi.org/10.1183/20734735.ELF152 Text en Copyright ©ERS 2019 http://creativecommons.org/licenses/by-nc/4.0/Breathe articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
spellingShingle ELF factsheet
IPF - Idiopathic Pulmonary Fibrosis
title IPF - Idiopathic Pulmonary Fibrosis
title_full IPF - Idiopathic Pulmonary Fibrosis
title_fullStr IPF - Idiopathic Pulmonary Fibrosis
title_full_unstemmed IPF - Idiopathic Pulmonary Fibrosis
title_short IPF - Idiopathic Pulmonary Fibrosis
title_sort ipf - idiopathic pulmonary fibrosis
topic ELF factsheet
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544798/
https://www.ncbi.nlm.nih.gov/pubmed/31191732
http://dx.doi.org/10.1183/20734735.ELF152

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