Idiopathic pulmonary fibrosis and systemic sclerosis-interstitial lung disease: features at admission to a tertiary pulmonology unit

Conclusion: Despite differences in epidemilogical and clinical features, patients with SSc-ILD and IPF share common functional features at presentation.

Source: European Respiratory Journal - October 28, 2020 Category: Respiratory Medicine Authors: Vettori, S., Lanza, M., Annunziata, A., Cauteruccio, R., Coppola, A., Di Spirito, V., De Simone, F., Gioia, S., Imitazione, P., Stefanelli, F., Fiorentino, G. Tags: ILD / DPLD of known origin Source Type: research