Evaluation of Patients with Fibrotic Interstitial Lung Disease: Preliminary results from the Turk-UIP Study
- Ebru, Cakir Edis
- Hatice, Turker
- Banu, Salepci
- Armagan, Hazar
- Yelda, Niksarlioglu Elif
- YILMAZ KARA, BİLGE
- KÖKTÜRK, NURDAN
- Fusun, Kalpaklioglu
- Isil, Uzel
- Savas, Ozsu
- Ersan, Atahan
- Zeynep, Fendoglu Turkan
- Sureyya, Yilmaz
- Ilknur, Basyigit
- Gungor, Camsari
- Esin, Tuncay
- Elif, Ucar Yilmazel
- Dilek, Kanmaz
- Aydanur, Ekici
- Fusun, Topcu
- Esra, Uzaslan
- Fulsen, Bozkus
- ARGUN BARIŞ, SERAP
- Serap, Duru
- Goksel, Altinisik
- Zuleyha, Bingol
- Atadan, Tunaci
- SAVAŞ, RECEP
- Fatih, Alper
- Selen, Bayraktaroglu
- Tuba, Selcuk Can
- Arslan, Demir Ali
- Benan, Musellim
- Nesrin, Mogulkoc
- Oguz, Uzun
- Fatma, Tokgoz Akyil
- Haluk, Turktas
- Ozlem, Ozdemir Kumbasar
- Gulfer, Okumus
- Candan, Ogus
- Hulya, Dirol
- Adil, Zamani
- Tulin, Sevim
- Nihat, Annakkaya Ali
- Akinci, Ozyurek Berna
- Ismail, Hanta
- Yusuf, Aydemir
- Bahar, Kurt
- Can, Tertemiz Kemal
- Levent, Tabak
- Onur, Yazici
- Yurdanur, Erdogan
- Gungor, Ates
DOIAbstract
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
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