A Commentary on the Role of Pulmonary Function Parameters in Idiopathic Pulmonary Fibrosis Follow‐Up
Author:
Affiliation:
1. Department of Pulmonology Health Science University, Yedikule Chest Diseases and Thoracic Surgery Training and Research Hospital Istanbul Turkey
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/crj.13797
Reference7 articles.
1. EMPIRE Registry, Czech Part: Impact of demographics, pulmonary function and HRCT on survival and clinical course in idiopathic pulmonary fibrosis
2. Pretreatment rate of decay in forced vital capacity predicts long-term response to pirfenidone in patients with idiopathic pulmonary fibrosis
3. Idiopathic Pulmonary Fibrosis (an Update) and Progressive Pulmonary Fibrosis in Adults: An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline
4. Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis
5. A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis
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