Idiopathic fibrotic lung disease at a university hospital setting: management and prognostic factors
Author:
Affiliation:
1. Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden
Publisher
Informa UK Limited
Subject
Pulmonary and Respiratory Medicine
Link
https://www.tandfonline.com/doi/pdf/10.3402/ecrj.v2.26915
Reference20 articles.
1. Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med. 2011; 183: 788–824.
2. Travis WD, Costabel U, Hansell DM, King TE Jr., Lynch DA, Nicholson AG. An official American Thoracic Society/European Respiratory Society statement: update of the international multidisciplinary classification of the idiopathic interstitial pneumonias. Am J Respir Crit Care Med. 2013; 188: 733–48.
3. Bradley B, Branley HM, Egan JJ, Greaves MS, Hansell DM, Harrison NK. Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society. Thorax. 2008; 63(Suppl 5): v1–58. [PubMed Abstract].
4. Flaherty KR, King TE Jr., Raghu G, Lynch JP 3rd, Colby TV, Travis WD. Idiopathic interstitial pneumonia: what is the effect of a multidisciplinary approach to diagnosis? Am J Respir Crit Care Med. 2004; 170: 904–10.
5. Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment
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