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Pediatric Pulmonology|October 19, 2011
Bronchodilator responsiveness in wheezy infants and toddlers is not associated with asthma risk factorsJason Debley, Sanja Stanojevic, Amy G Filbrun, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 11, 2019
Incidence and risk factors of paediatric cystic fibrosis-related diabetesLucy Perrem, Sanja Stanojevic, Melinda Solomon, et al.Respirology (Carlton, Vic.)|January 22, 2015
Effect of equipment dead space on multiple breath washout measuresAnouk Benseler, Sanja Stanojevic, Renee Jensen, et al.ERJ Open Research|February 12, 2019
Does the multiple-breath washout test need to be measured before spirometry?Jacky W Y Au, Reginald McDonald, Sanja Stanojevic, et al.ERJ Open Research|September 10, 2025
The utility of spirometry and single breath gas transfer measurements to identify low total lung capacityBen Knox-Brown, Chara Alexiou, Sanja Stanojevic, et al.Presse Medicale (Paris, France : 1983)|May 31, 2017
The changing epidemiology and demography of cystic fibrosisAnne L Stephenson, Sanja Stanojevic, Jenna Sykes, et al.Annals of the American Thoracic Society|March 16, 2019
Oral Azithromycin and Response to Pulmonary Exacerbations Treated with Intravenous Tobramycin in Children with Cystic FibrosisMichelle Klingel, Sanja Stanojevic, Elizabeth Tullis, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 25, 2017
Use of FEV<sub>1</sub> in cystic fibrosis epidemiologic studies and clinical trials: A statistical perspective for the clinical researcherRhonda Szczesniak, Sonya L Heltshe, Sanja Stanojevic, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|April 11, 2019
Linking COPD epidemiology with pediatric asthma care: Implications for the patient and the physicianErik Melén, Stefano Guerra, Jenny Hallberg, et al.Respiratory Medicine|February 10, 2016
A randomized controlled trial to evaluate the lung clearance index as an outcome measure for early phase studies in patients with cystic fibrosisReshma Amin, Sanja Stanojevic, Mica Kane, et al.Pageof 22