Research graph
References from Airway imaging practices in primary ciliary dyskinesia: a global survey to guide standardized guidelines. Local targets link to admitted publications; unresolved targets remain external evidence.
Genetic disorders of mucociliary clearance consortium. Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state-of-the-art review
10.1002/ppul.23304 · 2016 · External reference
Clinical practice guidelines from the cystic fibrosis foundation for preschoolers with cystic fibrosis
10.1542/peds.2015-1784 · 2016 · External reference
ECFS best practice guidelines: the 2018 revision
10.1016/j.jcf.2018.02.006 · 2018 · External reference
Beyond the present: current and future perspectives on the role of infections in pediatric PCD
10.3389/fped.2025.1564156 · 2025 · External reference
Treatment recommendations in primary ciliary dyskinesia
10.1016/j.prrv.2015.10.002 · 2016 · External reference
Unresolved reference
External reference
Pulmonary exacerbations in patients with primary ciliary dyskinesia: an expert consensus definition for use in clinical trials
10.1183/23120541.00147-2018 · 2019 · External reference
The cystic fibrosis foundation patient registry as a tool for use in quality improvement
10.1136/bmjqs-2013-002378 · 2014 · External reference
The diagnostic utility of artificial intelligence-guided computed tomography-based severity scores for predicting short-term clinical outcomes in adults with COVID-19 pneumonia
10.3390/jcm12227039 · 2023 · External reference
A fully automatic artificial intelligence–based CT image analysis system for accurate detection, diagnosis, and quantitative severity evaluation of pulmonary tuberculosis
10.1007/s00330-021-08365-z · 2022 · External reference
Artificial intelligence and COVID-19 using chest CT scan and chest X-ray images: machine learning and deep learning approaches for diagnosis and treatment
10.3390/jpm11100993 · 2021 · External reference
Automated CT scan scores of bronchiectasis and air trapping in cystic fibrosis
10.1378/chest.13-0588 · 2014 · External reference
