Assessment of Probability of Pulmonary Fibrosis Progression in Patients with Interstitial Lung Diseases to Determine Further Treatment Tactics
Author:
Affiliation:
1. Belarusian State Medical University
2. Republican Clinical Medical Center Administration of President of Belarus
3. Republican Scientific and Practical Center of Pulmonology and Phthisiology
Abstract
Publisher
LLC "Medical Knowledge and Technologies"
Reference14 articles.
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2. Arnott J.A., Lambi A.G., Mundy C. et al. The role of connective tissue growth factor (CTGF/CCN2) in skeletogenesis. Critical Reviews in Eukaryotic Gene Expression, 2011, vol. 21, no. 1, pp. 43-69.
3. Behr J., Günther A., Bonella F. German guideline for idiopathic pulmonary fibrosis. Pneumologie, 2020, vol. 74, pp. 263-293.
4. Bradley B., Branley H.M., Egan J.J. et al. 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, vol. 63, suppl. 5, pp. 1-58.
5. Cottin V., Hirani N.A., Hotchkin D.L. Presentation, diagnosis and clinical course of the spectrum of progressive-fibrosing interstitial lung diseases. Eur. Respir. Rev., 2018, vol. 27, no. 150, pp. 180076. https://doi.org/10.1183/16000617.0076-2018
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