Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Ratjen

Showing results (51-60 of 79) with videos related to

Pageof 8
Sort By:
Pediatric Pulmonology|November 9, 2004
DNA concentrations in BAL fluid of cystic fibrosis patients with early lung disease: influence of treatment with dornase alphaF Ratjen, K Paul, S van Koningsbruggen, et al.
American Journal of Respiratory and Critical Care Medicine|December 9, 2000
Airway nitric oxide levels in cystic fibrosis patients are related to a polymorphism in the neuronal nitric oxide synthase geneH Grasemann, N Knauer, R Büscher, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|September 1, 1989
Effect of changes in lung volume on respiratory system compliance in newborn infantsF Ratjen, R Zinman, A R Stark, et al.
The European Respiratory Journal|January 11, 2005
Oral L-arginine supplementation in cystic fibrosis patients: a placebo-controlled studyH Grasemann, C Grasemann, F Kurtz, et al.
European Journal of Pediatrics|November 1, 1985
A double-blind placebo controlled trial with oral ambroxol and N-acetylcysteine for mucolytic treatment in cystic fibrosisF Ratjen, R Wönne, H G Posselt, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 9, 2005
Prospective evaluation of emerging bacteria in cystic fibrosisG Steinkamp, B Wiedemann, E Rietschel, et al.
The Annals of Thoracic Surgery|December 5, 1997
Single-lung transplantation in a patient with cystic fibrosis and an asymmetric thoraxJ A Piotrowski, F H Splittgerber, T J Donovan, et al.
The European Respiratory Journal|June 3, 2000
Effect of L-arginine infusion on airway NO in cystic fibrosis and primary ciliary dyskinesia syndromeH Grasemann, S S Gärtig, H G Wiesemann, et al.
Pediatric Pulmonology|February 17, 2001
Effect of continuous antistaphylococcal therapy on the rate of P. aeruginosa acquisition in patients with cystic fibrosisF Ratjen, G Comes, K Paul, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2020
Infant spirometry as a predictor of lung function at early childhood in cystic fibrosis patientsM Pollak, M Shaw, S Balkovec, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
Pediatric Pulmonology|November 9, 2004
DNA concentrations in BAL fluid of cystic fibrosis patients with early lung disease: influence of treatment with dornase alphaF Ratjen, K Paul, S van Koningsbruggen, et al.
American Journal of Respiratory and Critical Care Medicine|December 9, 2000
Airway nitric oxide levels in cystic fibrosis patients are related to a polymorphism in the neuronal nitric oxide synthase geneH Grasemann, N Knauer, R Büscher, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|September 1, 1989
Effect of changes in lung volume on respiratory system compliance in newborn infantsF Ratjen, R Zinman, A R Stark, et al.
The European Respiratory Journal|January 11, 2005
Oral L-arginine supplementation in cystic fibrosis patients: a placebo-controlled studyH Grasemann, C Grasemann, F Kurtz, et al.
European Journal of Pediatrics|November 1, 1985
A double-blind placebo controlled trial with oral ambroxol and N-acetylcysteine for mucolytic treatment in cystic fibrosisF Ratjen, R Wönne, H G Posselt, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 9, 2005
Prospective evaluation of emerging bacteria in cystic fibrosisG Steinkamp, B Wiedemann, E Rietschel, et al.
The Annals of Thoracic Surgery|December 5, 1997
Single-lung transplantation in a patient with cystic fibrosis and an asymmetric thoraxJ A Piotrowski, F H Splittgerber, T J Donovan, et al.
The European Respiratory Journal|June 3, 2000
Effect of L-arginine infusion on airway NO in cystic fibrosis and primary ciliary dyskinesia syndromeH Grasemann, S S Gärtig, H G Wiesemann, et al.
Pediatric Pulmonology|February 17, 2001
Effect of continuous antistaphylococcal therapy on the rate of P. aeruginosa acquisition in patients with cystic fibrosisF Ratjen, G Comes, K Paul, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 21, 2020
Infant spirometry as a predictor of lung function at early childhood in cystic fibrosis patientsM Pollak, M Shaw, S Balkovec, et al.
Pageof 8