A Literature Review of Most Common Symptoms in Respiratory Therapist\'s Practice: How to Manage Dyspnea in Interstitial Lung Disease
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Publisher
Jaypee Brothers Medical Publishing
Link
https://www.ijrc.in/doi/pdf/10.5005/jp-journals-11010-1092
Reference26 articles.
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2. 2. Travis WD, Costabel U, Hansell DM, et al. 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(6):733–748. DOI: 10.1164/rccm.201308-1483ST
3. 3. Collard HR, King TE Jr, Bartelson BB, et al. Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2003;168(5):538–542. DOI: 10.1164/rccm.200211-1311OC
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5. 5. Swigris JJ, Brown KK, Behr J, et al. The SF-36 and SGRQ: validity and first look at minimum important differences in IPF. Respir Med 2010;104(2):296–304. DOI: 10.1016/j.rmed.2009.09.006
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