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Idiopathic and immune‐related pulmonary fibrosis: diagnostic and therapeutic challenges
Interstitial lung disease (ILD) encompasses a large group of pulmonary conditions sharing common clinical, radiological and histopathological features as a consequence of fibrosis of the lung interstitium. The majority of ILDs are idiopathic in nature with possible genetic predisposition, but is als...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831929/ https://www.ncbi.nlm.nih.gov/pubmed/31709050 http://dx.doi.org/10.1002/cti2.1086 |