Exercise Tolerance in Patients With Idiopathic Pulmonary Fibrosis, Effect of Supplemental Oxygen
Author:
Affiliation:
1. Department of Respiratory Diseases, Thomayer Hospital, First Faculty of Medicine, Charles University, Prague, Czech Republic. jan.chlumsky@ftn.cz
Abstract
Publisher
Institute of Physiology of the Czech Academy of Sciences
Subject
General Medicine,Physiology
Reference15 articles.
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2. DiMarco AF, Kelsen SG, Cherniack NS, Gothe B. Occlusion pressure and breathing pat-tern in patients with interstitial lung disease. Am Rev Respir Dis 1983;127(4):425-430. https://doi.org/10.1164/arrd.1983.127.4.425
3. Schaeffer MR, Ryerson CJ, Ramsook AH, et al. Neurophysiological mechanisms of exer-tional dyspnoea in fibrotic interstitial lung disease. Eur Respir J 2018;51:1701726. https://doi.org/10.1183/13993003.01726-2017
4. Agustí AGN, Roca J, Gea J, Wagner PD, Xaubet A, Rodriguez-Roisin R. Mechanisms of Gas-exchange Impairment in Idiopathic Pulmonary Fibrosis. Am Rev Respir Dis 1991;143(2):219-225. https://doi.org/10.1164/ajrccm/143.2.219
5. Hallstrand TS, Boitano LJ, Johnson WC, Spada C, Hayes JG, Raghu G. The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis. Eur Respir J 2005;25(1):96-103. https://doi.org/10.1183/09031936.04.00137203
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