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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...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:J Scleroderma Relat Disord
1. Verfasser: Volkmann, Elizabeth R
Format: Artigo
Sprache:Inglês
Veröffentlicht: SAGE Publications 2019
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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