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Felix Ratjen

Showing results (131-140 of 385) with videos related to

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Annals of the American Thoracic Society|September 13, 2024
The Impact of Age of Diagnosis in Children with Primary Ciliary DyskinesiaDvir Gatt, Michelle Shaw, Fiona Kritzinger, et al.
The Journal of Pediatrics|April 26, 2011
Diagnostic value of nasal nitric oxide measured with non-velum closure techniques for children with primary ciliary dyskinesiaDimas Mateos-Corral, Robin Coombs, Hartmut Grasemann, et al.
Canadian Respiratory Journal|April 28, 2010
Pediatric Respiratory Assembly. Mini symposium on lung inflammationLarry C Lands, A Keith Tanswell, Sophie Laberge, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 15, 2015
Effect of ivacaftor therapy on exhaled nitric oxide in patients with cystic fibrosisHartmut Grasemann, Tanja Gonska, Julie Avolio, et al.
Journal of Personalized Medicine|June 2, 2021
The Equitable Implementation of Cystic Fibrosis Personalized Medicines in CanadaGenevieve Shemie, Minh Thu Nguyen, John Wallenburg, et al.
American Journal of Respiratory and Critical Care Medicine|August 12, 2017
Reply to Verbanck and Vanderhelst: The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic FibrosisNikhil Kanhere, Marcus J Couch, Jonathan H Rayment, et al.
Annals of the American Thoracic Society|February 8, 2023
Efficacy of Antibiotic Eradication Therapy of Early <i>Pseudomonas aeruginosa</i> Infection in Children with Primary Ciliary DyskinesiaDvir Gatt, Michelle Shaw, Wallace Wee, et al.
Expert Review of Respiratory Medicine|July 25, 2023
The argument for utilising magnetic resonance imaging as a tool for monitoring lung structure and function in pediatric patientsBrandon Zanette, Mary-Louise C Greer, Theo J Moraes, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 20, 2023
Factors associated with lung function response with oral antibiotic treatment of pulmonary exacerbations in cystic fibrosisAna C Blanchard, Michelle Shaw, Felix Ratjen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 7, 2020
Changes in the parent cystic fibrosis questionnaire-revised (CFQ-R) with respiratory symptoms in preschool children with cystic fibrosisLucy Perrem, Sanja Stanojevic, Michelle Shaw, et al.
Pageof 39

Showing results (131-140 of 385) with videos related to

Sort By:
Pageof 39
Annals of the American Thoracic Society|September 13, 2024
The Impact of Age of Diagnosis in Children with Primary Ciliary DyskinesiaDvir Gatt, Michelle Shaw, Fiona Kritzinger, et al.
The Journal of Pediatrics|April 26, 2011
Diagnostic value of nasal nitric oxide measured with non-velum closure techniques for children with primary ciliary dyskinesiaDimas Mateos-Corral, Robin Coombs, Hartmut Grasemann, et al.
Canadian Respiratory Journal|April 28, 2010
Pediatric Respiratory Assembly. Mini symposium on lung inflammationLarry C Lands, A Keith Tanswell, Sophie Laberge, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 15, 2015
Effect of ivacaftor therapy on exhaled nitric oxide in patients with cystic fibrosisHartmut Grasemann, Tanja Gonska, Julie Avolio, et al.
Journal of Personalized Medicine|June 2, 2021
The Equitable Implementation of Cystic Fibrosis Personalized Medicines in CanadaGenevieve Shemie, Minh Thu Nguyen, John Wallenburg, et al.
American Journal of Respiratory and Critical Care Medicine|August 12, 2017
Reply to Verbanck and Vanderhelst: The Respective Roles of Lung Clearance Index and Magnetic Resonance Imaging in the Clinical Management of Patients with Cystic FibrosisNikhil Kanhere, Marcus J Couch, Jonathan H Rayment, et al.
Annals of the American Thoracic Society|February 8, 2023
Efficacy of Antibiotic Eradication Therapy of Early <i>Pseudomonas aeruginosa</i> Infection in Children with Primary Ciliary DyskinesiaDvir Gatt, Michelle Shaw, Wallace Wee, et al.
Expert Review of Respiratory Medicine|July 25, 2023
The argument for utilising magnetic resonance imaging as a tool for monitoring lung structure and function in pediatric patientsBrandon Zanette, Mary-Louise C Greer, Theo J Moraes, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 20, 2023
Factors associated with lung function response with oral antibiotic treatment of pulmonary exacerbations in cystic fibrosisAna C Blanchard, Michelle Shaw, Felix Ratjen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 7, 2020
Changes in the parent cystic fibrosis questionnaire-revised (CFQ-R) with respiratory symptoms in preschool children with cystic fibrosisLucy Perrem, Sanja Stanojevic, Michelle Shaw, et al.
Pageof 39