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ERJ Open Research|March 15, 2021
Chest physiotherapy enhances detection of Pseudomonas aeruginosa in nonexpectorating children with cystic fibrosisChristophe Marguet, Véronique Houdouin, Isabelle Pin, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 2, 2021
"Il faut continuer à poser des questions" patient reported outcome measures in cystic fibrosis: An anthropological perspectiveRosa Coucke, Audrey Chansard, Véronique Bontemps, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 3, 2014
Comparing Mycobacterium massiliense and Mycobacterium abscessus lung infections in cystic fibrosis patientsAnne-Laure Roux, Emilie Catherinot, Nathalie Soismier, et al.Journal of Medical Genetics|January 23, 2013
Asphyxiating thoracic dysplasia: clinical and molecular review of 39 familiesGeneviève Baujat, Céline Huber, Joyce El Hokayem, et al.ERJ Open Research|June 18, 2026
Persistence of lung hyperinflation and small airway dysfunction in school-aged children with cystic fibrosis treated with elexacaftor-tezacaftor-ivacaftor: results from the real-world MODUL-CF studyLucie Colin, Véronique Delaup, Muriel Le Bourgeois, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 10, 2014
Central venous thrombosis and thrombophilia in cystic fibrosis: A prospective studyAnne Munck, Ahmed Kheniche, Corinne Alberti, et al.Medicine|July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national surveyMarie-Olivia Chandesris, Isabelle Melki, Angels Natividad, et al.The European Respiratory Journal|February 16, 2023
The French compassionate programme of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis with advanced lung disease and no F508del CFTR variantPierre-Régis Burgel, Isabelle Sermet-Gaudelus, Isabelle Durieu, et al.Pageof 6