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Pathogenetic mechanisms in usual interstitial pneumonia/idiopathic pulmonary fibrosis
Idiopathic pulmonary fibrosis (IPF) is a progressive, usually fatal, form of interstitial lung disease characterized by failure of alveolar re-epithelialization, persistence of fibroblasts/myofibroblasts, deposition of extracellular matrix, and distortion of lung architecture which ultimately result...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2003
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2810622/ https://ncbi.nlm.nih.gov/pubmed/14595745 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/path.1446 |
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