Idiopathic Pulmonary Fibrosis Well-Controlled in Progress Good Control for a Long Interval with Pirfenidone: a Case Report
Author:
Affiliation:
1. Division of Respiratory Medicine, Department of Internal Medicine, Nihon University School of Medicine
2. Department of Respiratory Medicine, Itabashi Medical Association Hospital
Publisher
The Nihon University Medical Association
Link
https://www.jstage.jst.go.jp/article/numa/74/2/74_69/_pdf
Reference12 articles.
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2. 2) Costabel U, King TE. International consensus statement on idiopathic pulmonary fibrosis. Eur Respir J 2001; 17: 163-167.
3. 3) Fern-ndez P-rez ER, Daniels CE, Schroeder DR, et al. Incidence, prevalence, and clinical course of idiopathic pulmonary fibrosis: a population-based study. Chest 2010; 137: 129-137.
4. 4) Selman M, King TE, Pardo A. Idiopathic pulmonary fibrosis: prevailing and evolving hypotheses about its pathogenesis and implications for therapy. Ann Intern Med 2001; 134: 136-151.
5. 5) King TE Jr, Tooze JA, Schwarz MI, et al. Predicting survival in idiopathic pulmonary fibrosis: scoring system and survival model. Am J Respir Crit Care Med 2001; 164: 1171-1181.
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1. Distinct improvement of pulmonary function, ground-glass opacity, hypoxia and physical findings in an idiopathic pulmonary fibrosis patient after pirfenidone treatment : a case report with a review of the literature;The Journal of Medical Investigation;2020
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