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

Bruce C Marshall

Showing results (21-30 of 92) with videos related to

Pageof 10
Sort By:
Respiratory Medicine|February 3, 2022
When is cystic fibrosis not cystic fibrosis? The importance of appropriately classifying patientsAlbert Faro, Christopher Goss, Elizabeth Cromwell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 25, 2022
Telehealth and CFTR modulators: Accelerating innovative models of cystic fibrosis careMichelle H Prickett, Patrick A Flume, Kathryn A Sabadosa, et al.
BMJ Quality & Safety|March 11, 2014
Key findings of the US Cystic Fibrosis Foundation's clinical practice benchmarking projectMichael P Boyle, Kathryn A Sabadosa, Hebe B Quinton, et al.
Pediatrics|May 3, 2002
Influenza vaccination coverage level at a cystic fibrosis centerBruce C Marshall, Carmen Henshaw, Dee Anne Evans, et al.
Pediatric Pulmonology|September 15, 2017
Data that empower: The success and promise of CF patient registriesAliza K Fink, Deena R Loeffler, Bruce C Marshall, et al.
The Journal of Pediatrics|June 26, 2007
Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelinesVicky A LeGrys, James R Yankaskas, Lynne M Quittell, et al.
Pediatric Pulmonology|May 1, 2007
Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypesDao Nguyen, Mary J Emond, Nicole Mayer-Hamblett, et al.
American Journal of Respiratory and Critical Care Medicine|August 3, 2010
Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothoraxPatrick A Flume, Peter J Mogayzel, Karen A Robinson, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 5, 2010
The application of current lifetable methods to compare cystic fibrosis median survival internationally is limitedAbaigeal D Jackson, Leslie Daly, Cecily Kelleher, et al.
Chest|July 25, 2007
Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosisChristian A Merlo, Michael P Boyle, Marie Diener-West, et al.
Pageof 10

Showing results (21-30 of 92) with videos related to

Sort By:
Pageof 10
Respiratory Medicine|February 3, 2022
When is cystic fibrosis not cystic fibrosis? The importance of appropriately classifying patientsAlbert Faro, Christopher Goss, Elizabeth Cromwell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 25, 2022
Telehealth and CFTR modulators: Accelerating innovative models of cystic fibrosis careMichelle H Prickett, Patrick A Flume, Kathryn A Sabadosa, et al.
BMJ Quality & Safety|March 11, 2014
Key findings of the US Cystic Fibrosis Foundation's clinical practice benchmarking projectMichael P Boyle, Kathryn A Sabadosa, Hebe B Quinton, et al.
Pediatrics|May 3, 2002
Influenza vaccination coverage level at a cystic fibrosis centerBruce C Marshall, Carmen Henshaw, Dee Anne Evans, et al.
Pediatric Pulmonology|September 15, 2017
Data that empower: The success and promise of CF patient registriesAliza K Fink, Deena R Loeffler, Bruce C Marshall, et al.
The Journal of Pediatrics|June 26, 2007
Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelinesVicky A LeGrys, James R Yankaskas, Lynne M Quittell, et al.
Pediatric Pulmonology|May 1, 2007
Clinical response to azithromycin in cystic fibrosis correlates with in vitro effects on Pseudomonas aeruginosa phenotypesDao Nguyen, Mary J Emond, Nicole Mayer-Hamblett, et al.
American Journal of Respiratory and Critical Care Medicine|August 3, 2010
Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothoraxPatrick A Flume, Peter J Mogayzel, Karen A Robinson, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 5, 2010
The application of current lifetable methods to compare cystic fibrosis median survival internationally is limitedAbaigeal D Jackson, Leslie Daly, Cecily Kelleher, et al.
Chest|July 25, 2007
Incidence and risk factors for multiple antibiotic-resistant Pseudomonas aeruginosa in cystic fibrosisChristian A Merlo, Michael P Boyle, Marie Diener-West, et al.
Pageof 10