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ERJ Open Research|April 27, 2023
Diffuse alveolar haemorrhage in children: an international multicentre studyAstrid Madsen Ring, Nicolaus Schwerk, Nural Kiper, et al.European Journal of Pediatrics|April 1, 2026
Quality of life in Turkish children with interstitial lung disease: Insights from the National chILD RegistryHandan Kekec, Tugba Sismanlar Eyuboglu, Ayse Tana Aslan, et al.The Lancet. Respiratory Medicine|June 24, 2026
Prevalence and disease trajectories of pulmonary fibrosis of childhood interstitial lung disease: a register-based, multicentre observational studyMatthias Griese, Simone Reu-Hofer, Julia Ley-Zaporozhan, et al.Pediatric Pulmonology|November 12, 2019
Cystic fibrosis in Turkey: First data from the national registryDeniz Dogru, Erkan Çakır, Tuğba Şişmanlar, et al.Pediatric Pulmonology|May 5, 2020
Clinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosisTugba Sismanlar Eyuboglu, Deniz Dogru, Erkan Çakır, et al.Pediatric Pulmonology|May 27, 2020
Patients eligible for modulator drugs: Data from cystic fibrosis registry of TurkeyNazan Çobanoğlu, Uğur Özçelik, Erkan Çakır, et al.European Journal of Pediatrics|October 24, 2023
Childhood interstitial lung disease in Turkey: first data from the national registryHalime Nayır-Büyükşahin, Nagehan Emiralioğlu, Ayşe Ayzıt Kılınç, et al.Pediatric Pulmonology|June 6, 2023
Patients with cystic fibrosis who could not receive the CFTR modulator treatment: What did they lose in 1 year?Salih Uytun, Güzin Cinel, Sanem Eryılmaz Polat, et al.The Turkish Journal of Pediatrics|April 28, 2023
Clinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry dataZeynep Reyhan Onay, Tuğba Şismanlar Eyüboğlu, Ayşe Tana Aslan, et al.Pediatric Pulmonology|July 9, 2024
Factors associated with pulmonary function decline of patients in the cystic fibrosis registry of Turkey: A retrospective cohort studyNagehan Emiralioğlu, Banu Çakır, Ahmet Sertçelik, et al.Pageof 19