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Natural history of systemic sclerosis–related interstitial lung disease: How to identify a progressive fibrosing phenotype
The natural history of interstitial lung disease in patients with systemic sclerosis is highly variable. Historical observational studies have demonstrated that the greatest decline in lung function in systemic sclerosis occurs early in the course of the disease; however, not all patients experience...
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| Veröffentlicht in: | J Scleroderma Relat Disord |
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| 1. Verfasser: | |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
SAGE Publications
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7943063/ https://ncbi.nlm.nih.gov/pubmed/33693056 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2397198319889549 |
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