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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...
Enregistré dans:
| Publié dans: | J Scleroderma Relat Disord |
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| Auteur principal: | |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
SAGE Publications
2019
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| Sujets: | |
| Accès en ligne: | 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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