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Idiopathic pulmonary fibrosis

Published:2017-10-20 Issue:1 Volume:3 Page:
ISSN:2056-676X
Container-title:Nature Reviews Disease Primers
language:en
Short-container-title:Nat Rev Dis Primers

Author:

Martinez Fernando J.,Collard Harold R.,Pardo Annie,Raghu Ganesh,Richeldi Luca,Selman Moises,Swigris Jeffrey J.,Taniguchi Hiroyuki,Wells Athol U.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Link

http://www.nature.com/articles/nrdp201774.pdf

Reference251 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 (2011). This multinational expert panel reviews the available data for the diagnosis and management of patients with IPF, providing an evidence-based series of recommendations for patients and clinicians.

2. Kim, H. J., Perlman, D. & Tomic, R. Natural history of idiopathic pulmonary fibrosis. Respir. Med. 109, 661–670 (2015).

3. Wu, X., Kaner, R. J. & Martinez, F. J. Idiopathic pulmonary fibrosis: what is the best treatment? BRN Rev. 3, 86–101 (2017).

4. King, T. E., Pardo, A. & Selman, M. Idiopathic pulmonary fibrosis. Lancet 378, 1949–1961 (2011).

5. Baddini-Martinez, J. & Pereira, C. A. How many patients with idiopathic pulmonary fibrosis are there in Brazil? J. Bras. Pneumol 41, 560–561 (2015).

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