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Diagnosis of Idiopathic Pulmonary Fibrosis: Differential Diagnosis
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and fibrotic interstitial lung disease of unknown origin with a characteristic imaging and histologic pattern called usual interstitial pneumonia (UIP). The diagnosis of IPF is a complex procedure that requires the support of various spe...
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| Udgivet i: | Med Sci (Basel) |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
MDPI
2018
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6164303/ https://ncbi.nlm.nih.gov/pubmed/30181506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/medsci6030073 |
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