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

Clement L Ren

Showing results (71-80 of 123) with videos related to

Pageof 13
Sort By:
Pediatric Pulmonology|October 11, 2008
The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosisGregory S Sawicki, Lawrence Rasouliyan, David J Pasta, et al.
Pediatric Pulmonology|July 10, 2008
Trends in the clinical characteristics of the U.S. cystic fibrosis patient population from 1995 to 2005Donald R VanDevanter, Lawrence Rasouliyan, Thomas M Murphy, et al.
The Journal of Pediatrics|July 27, 2020
Early Neonatal Oxygen Exposure Predicts Pulmonary Morbidity and Functional Deficits at 1 YearAndrew M Dylag, Hannah G Kopin, Michael A O'Reilly, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 31, 2025
Impact of CFTR modulator therapy on basic life needs and financial concerns in people with cystic fibrosis: Data from the Well-ME surveyHeather Boas, Aricca D Van Citters, Elizabeth L Yu, et al.
Pediatric Pulmonology|July 7, 2022
Forced expiratory flows and diffusion capacity in infants born from mothers with pre-eclampsiaClement L Ren, James E Slaven, David M Haas, et al.
Pediatric Pulmonology|June 18, 2021
Hyperinflation is associated with increased respiratory rate and is a more sensitive measure of cystic fibrosis lung disease during infancy compared to forced expiratory measuresHeather N Muston, James E Slaven, Christina Tiller, et al.
Annals of the American Thoracic Society|November 11, 2016
Diagnostic Evaluation of Infants with Recurrent or Persistent WheezingDebra Boyer, Emily Barsky, Christina Michelle Papantonakis, et al.
Pediatric Pulmonology|May 1, 2007
Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung functionClement L Ren, Wayne J Morgan, Michael W Konstan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 22, 2021
Comment on Munck et al., Feb, 2021Marci K Sontag, Phillip M Farrell, Yvonne Kellar-Guenther, et al.
Pediatric Pulmonology|July 12, 2024
Treatment of small as well as large declines in lung function enhances recovery to baseline in people with CFMichael S Schechter, Joshua S Ostrenga, Elizabeth A Cromwell, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
Pediatric Pulmonology|October 11, 2008
The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosisGregory S Sawicki, Lawrence Rasouliyan, David J Pasta, et al.
Pediatric Pulmonology|July 10, 2008
Trends in the clinical characteristics of the U.S. cystic fibrosis patient population from 1995 to 2005Donald R VanDevanter, Lawrence Rasouliyan, Thomas M Murphy, et al.
The Journal of Pediatrics|July 27, 2020
Early Neonatal Oxygen Exposure Predicts Pulmonary Morbidity and Functional Deficits at 1 YearAndrew M Dylag, Hannah G Kopin, Michael A O'Reilly, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 31, 2025
Impact of CFTR modulator therapy on basic life needs and financial concerns in people with cystic fibrosis: Data from the Well-ME surveyHeather Boas, Aricca D Van Citters, Elizabeth L Yu, et al.
Pediatric Pulmonology|July 7, 2022
Forced expiratory flows and diffusion capacity in infants born from mothers with pre-eclampsiaClement L Ren, James E Slaven, David M Haas, et al.
Pediatric Pulmonology|June 18, 2021
Hyperinflation is associated with increased respiratory rate and is a more sensitive measure of cystic fibrosis lung disease during infancy compared to forced expiratory measuresHeather N Muston, James E Slaven, Christina Tiller, et al.
Annals of the American Thoracic Society|November 11, 2016
Diagnostic Evaluation of Infants with Recurrent or Persistent WheezingDebra Boyer, Emily Barsky, Christina Michelle Papantonakis, et al.
Pediatric Pulmonology|May 1, 2007
Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung functionClement L Ren, Wayne J Morgan, Michael W Konstan, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 22, 2021
Comment on Munck et al., Feb, 2021Marci K Sontag, Phillip M Farrell, Yvonne Kellar-Guenther, et al.
Pediatric Pulmonology|July 12, 2024
Treatment of small as well as large declines in lung function enhances recovery to baseline in people with CFMichael S Schechter, Joshua S Ostrenga, Elizabeth A Cromwell, et al.
Pageof 13