Clinical, Functional, and Prognostic Evaluation of Idiopathic Pulmonary Fibrosis, Connective Tissue Disease-AssociatedInterstitial Lung Disease, Interstitial Pneumonia with Autoimmune Features: A Single-Center Prospective Study

Öz, MİRAÇ; Erol, SERHAT; Küçükşahin, Orhan; Kar, İrem; Atasoy, Kayhan; Özdemir Kumbasar, ÖZLEM

doi:10.5152/turkthoracj.2022.22017

Clinical, Functional, and Prognostic Evaluation of Idiopathic Pulmonary Fibrosis, Connective Tissue Disease-AssociatedInterstitial Lung Disease, Interstitial Pneumonia with Autoimmune Features: A Single-Center Prospective Study

Atıf İçin Kopyala

Öz M., Erol S., Küçükşahin O., Kar İ., Atasoy K. Ç., Özdemir Kumbasar Ö.

Turkish Thoracic Journal, cilt.23, sa.6, ss.395-402, 2022 (ESCI)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 23 Sayı: 6
Basım Tarihi: 2022
Doi Numarası: 10.5152/turkthoracj.2022.22017
Dergi Adı: Turkish Thoracic Journal
Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI)
Sayfa Sayıları: ss.395-402
Anahtar Kelimeler: Interstitial lung diseases, collagen tissue diseases, IPF, IPAF, RHEUMATOLOGY/EUROPEAN LEAGUE, CLASSIFICATION CRITERIA, AMERICAN-COLLEGE, STANDARDIZATION, DIAGNOSIS
Ankara Üniversitesi Adresli: Evet

Özet

OBJECTIVE: Our study aimed to evaluate clinical, functional, and prognostic features and to determine the prognosis of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung diseases, and interstitial pneumonia with autoimmune features.