Idiopathic pulmonary fibrosis in a Swiss interstitial lung disease reference centre.

CONCLUSION: Registries for rare diseases such as IPF are a valuable resource for studying the course of the disease under current compliance with diagnostic and treatment guidelines and to appreciate local epidemiological particularities.
PMID: 29376545 [PubMed - in process]

Source: Swiss Medical Weekly - January 29, 2018 Category: General Medicine Authors: Guler S, Zumstein P, Berezowska S, Pöllinger A, Geiser T, Funke-Chambour M Tags: Swiss Med Wkly Source Type: research