Comparison of CPI and GAP models in patients with idiopathic pulmonary fibrosis: a nationwide cohort study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-018-23073-3.pdf
Reference33 articles.
1. Raghu, G. et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 183, 788–824, https://doi.org/10.1164/rccm.2009-040GL (2011).
2. Raghu, G. et al. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline: Treatment of Idiopathic Pulmonary Fibrosis. An Update of the 2011 Clinical Practice Guideline. Am J Respir Crit Care Med 192, e3–19, https://doi.org/10.1164/rccm.201506-1063ST (2015).
3. Ley, B., Collard, H. R. & King, T. E. Jr. Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 183, 431–440, https://doi.org/10.1164/rccm.201006-0894CI (2011).
4. Rozanski, C. & Mura, M. Multi-Dimensional Indeces to Stage Idiopathic Pulmonary Fibrosis: A Systematic Review. Sarcoidosis Vasc Dif 31, 8–18 (2014).
5. Gay, S. E. et al. Idiopathic pulmonary fibrosis - Predicting response to therapy and survival. Am J Resp Crit Care 157, 1063–1072 (1998).
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