Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study
Makaleler > Tam Makale · 2021
Yazarlar: Musellim Benan, Nesrin MOĞULKOÇ BISHOP, Uzun Oguz, Tokgoz Akyil Fatma, Turktas Haluk, Ozdemir Kumbasar Ozlem, Okumus Gulfer, Ogus Candan, Dirol Hulya, Zamani Adil, Sevim Tulin, Annakkaya Ali Nihat, Ozyurek Berna Akinci, Hanta Ismail, Aydemir Yusuf, Cakir Edis Ebru, Kurt Bahar, Tertemiz Kemal Can, Tabak Levent, Yazici Onur, Erdogan Yurdanur, Ates Gungor, Turker Hatice, Salepci Banu, Hazar Armagan, Niksarlioglu Elif Yelda, Bilge Yılmaz Kara, Nurdan Köktürk, Kalpaklioglu Fusun, Uzel Isil, Ozsu Savas, Atahan Ersan, Fendoglu Turkan Zeynep, Yilmaz Sureyya, Basyigit Ilknur, Camsari Gungor, Tuncay Esin, Ucar Yilmazel Elif, Kanmaz Dilek, Ekici Aydanur, Topcu Fusun, Uzaslan Esra, Bozkus Fulsen, Serap Argun Barış, Duru Serap, Altinisik Goksel, Bingol Zuleyha, Tunaci Atadan, Recep SAVAŞ, Alper Fatih, Selen BAYRAKTAROĞLU, Selcuk Can Tuba, Demir Ali Arslan
TURKISH THORACIC JOURNAL, SCI Expanded İndekslerine Giren Dergi, Uluslararası, 2021, cilt 22, ss 102-109
DOI: 10.5152/turkthoracj.2021.20028
Özet
OBJECTIVE: Differential diagnosis of idiopathic pulmonary fibrosis (IPF) is important among fibrotic interstitial lung diseases (ILD). This study aimed to evaluate the rate of IPF in patients with fibrotic ILD and to determine the clinical-laboratory features of patients with and without IPF that would provide the differential diagnosis of IPF.