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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|December 23, 2004
Measurement of immunoglobulin G against Mycobacterial antigen A60 in patients with cystic fibrosis and lung infection due to Mycobacterium abscessusAgnès Ferroni, Isabelle Sermet-Gaudelus, Muriel Le Bourgeois, et al.Pediatric Pulmonology|September 2, 2017
Early follow-up of lung disease in infants with cystic fibrosis using the raised volume rapid thoracic compression technique and computed tomography during quiet breathingRémi Gauthier, Yann Cabon, Marie Agnes Giroux-Metges, et al.Pediatric Radiology|March 7, 2014
Primary pulmonary alveolar proteinosis: computed tomography features at diagnosisLaureline Berteloot, Rola Abou Taam, Sophie Emond-Gonsard, et al.ERJ Open Research|December 31, 2025
Reversibility in plethysmographic airway and specific airway resistance in childrenNicole Beydon, Cécile Du Boisbaudry, Christophe Delclaux, et al.European Journal of Pediatrics|July 27, 2024
Radiation-free and injection-free imaging of the paediatric chest using a magnetic resonance imaging protocol including zero time echo sequence (3D-ZTE)David Drummond, Fabienne Marquant, Elisa Zanelli, et al.Pediatric Pulmonology|December 31, 2015
Eosinophilic pneumonias in children: A review of the epidemiology, diagnosis, and treatmentLisa Giovannini-Chami, Sibylle Blanc, Alice Hadchouel, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 1, 2006
Microbiological diagnosis of empyema in children: comparative evaluations by culture, polymerase chain reaction, and pneumococcal antigen detection in pleural fluidsAlban Le Monnier, Etienne Carbonnelle, Jean-Ralph Zahar, et al.European Journal of Pediatrics|February 5, 2025
Specific airway resistance according to early maternal vitamin D status during pregnancy in children aged 5 to 6 years old from the FEPED cohort (RESPIFEPED)Apolline Gonsard, Fabienne Marquant, Caroline Elie, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 24, 2016
Changes of CFTR functional measurements and clinical improvements in cystic fibrosis patients with non p.Gly551Asp gating mutations treated with ivacaftorMyriam Mesbahi, Michal Shteinberg, Michael Wilschanski, et al.The European Respiratory Journal|September 1, 2012
Inhaled therapies, azithromycin and Mycobacterium abscessus in cystic fibrosis patientsEmilie Catherinot, Anne-Laure Roux, Marie-Anne Vibet, et al.Pageof 6