Clinical features and prognosis of microscopic polyangiitis with usual interstitial pneumonia compared with idiopathic pulmonary fibrosis-Reference-Cited by-同舟云学术

Clinical features and prognosis of microscopic polyangiitis with usual interstitial pneumonia compared with idiopathic pulmonary fibrosis

Published:2019-05-16 Issue:7 Volume:13 Page:460-466
ISSN:1752-6981
Container-title:The Clinical Respiratory Journal
language:en
Short-container-title:Clin Respir J

Author:

Zhao Wen¹²,Dai Huaping¹³^ORCID,Liu Yan¹,Zhu Min¹,Bao Na⁴,Ban Chengjun¹,Zhang Shu¹,Ren Yanhong¹³,Ye Qiao¹,Wang Chen¹³

Affiliation:

1. Beijing Key Laboratory of Respiratory and Pulmonary Circulation Disorders, Department of Respiratory and Critical Care Medicine Beijing Chao‐Yang Hospital‐Beijing Institute of Respiratory Medicine, Capital Medical University Beijing P.R. China

2. Department of Respiratory Medicine Beijing Ditan Hospital, Capital Medical University Beijing P.R. China

3. Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine China–Japan Friendship Hospital, National Clinical Research Centre for Respiratory Medicine Beijing P.R. China

4. Department of Radiology and Image Beijing Chao‐Yang Hospital, Capital Medical University Beijing P.R. China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Pulmonary and Respiratory Medicine,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/crj.13032

Reference30 articles.

1. Treatment of interstitial lung diseases associated with connective tissue diseases

2. An Official ATS/ERS/JRS/ALAT Statement: Idiopathic Pulmonary Fibrosis: Evidence-based Guidelines for Diagnosis and Management