Načítá se...
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...
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| Vydáno v: | Clin Transl Immunology |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
John Wiley and Sons Inc.
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6831929/ https://ncbi.nlm.nih.gov/pubmed/31709050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cti2.1086 |
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