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

Drucy Borowitz

Showing results (51-60 of 77) with videos related to

Pageof 8
Sort By:
Journal of Pediatric Gastroenterology and Nutrition|April 20, 2022
Changes in Glucose Breath Test in Cystic Fibrosis Patients Treated With 1 Month of Lumacaftor/IvacaftorMegan E Gabel, Hongyue Wang, Daniel Gelfond, et al.
JAMA Pediatrics|April 25, 2017
Effects of Diagnosis by Newborn Screening for Cystic Fibrosis on Weight and Length in the First Year of LifeDaniel H Leung, Sonya L Heltshe, Drucy Borowitz, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 28, 2017
Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn ScreeningDaniel Gelfond, Sonya L Heltshe, Michelle Skalland, et al.
American Journal of Medical Genetics|September 20, 2002
Idiopathic congenital central hypoventilation syndrome: the next generationJean M Silvestri, Maida L Chen, Debra E Weese-Mayer, et al.
Journal of Medical Genetics|November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTRMolly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.
Clinical and Translational Science|June 9, 2015
Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter StudyChristine Coburn-Miller, Susan Casey, Quynh Luong, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 25, 2023
Incidence of fibrosing colonopathy with pancreatic enzyme replacement therapy in patients with cystic fibrosisStephanie E Chiuve, Daniel Fife, Gerhard Leitz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 27, 2018
RNA sequencing data from neutrophils of patients with cystic fibrosis reveals potential for developing biomarkers for pulmonary exacerbationsKaiyu Jiang, Kerry E Poppenberg, Laiping Wong, et al.
Pediatric Pulmonology|January 24, 2019
Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort studyDanielle Goetz, Benjamin T Kopp, Ann Salvator, et al.
Annals of the American Thoracic Society|July 10, 2020
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical TrialScott D Sagel, Umer Khan, Sonya L Heltshe, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Journal of Pediatric Gastroenterology and Nutrition|April 20, 2022
Changes in Glucose Breath Test in Cystic Fibrosis Patients Treated With 1 Month of Lumacaftor/IvacaftorMegan E Gabel, Hongyue Wang, Daniel Gelfond, et al.
JAMA Pediatrics|April 25, 2017
Effects of Diagnosis by Newborn Screening for Cystic Fibrosis on Weight and Length in the First Year of LifeDaniel H Leung, Sonya L Heltshe, Drucy Borowitz, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 28, 2017
Pancreatic Enzyme Replacement Therapy Use in Infants With Cystic Fibrosis Diagnosed by Newborn ScreeningDaniel Gelfond, Sonya L Heltshe, Michelle Skalland, et al.
American Journal of Medical Genetics|September 20, 2002
Idiopathic congenital central hypoventilation syndrome: the next generationJean M Silvestri, Maida L Chen, Debra E Weese-Mayer, et al.
Journal of Medical Genetics|November 25, 2010
CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTRMolly B Sheridan, Timothy W Hefferon, Nulang Wang, et al.
Clinical and Translational Science|June 9, 2015
Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter StudyChristine Coburn-Miller, Susan Casey, Quynh Luong, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 25, 2023
Incidence of fibrosing colonopathy with pancreatic enzyme replacement therapy in patients with cystic fibrosisStephanie E Chiuve, Daniel Fife, Gerhard Leitz, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 27, 2018
RNA sequencing data from neutrophils of patients with cystic fibrosis reveals potential for developing biomarkers for pulmonary exacerbationsKaiyu Jiang, Kerry E Poppenberg, Laiping Wong, et al.
Pediatric Pulmonology|January 24, 2019
Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort studyDanielle Goetz, Benjamin T Kopp, Ann Salvator, et al.
Annals of the American Thoracic Society|July 10, 2020
Clinical Effectiveness of Lumacaftor/Ivacaftor in Patients with Cystic Fibrosis Homozygous for F508del-CFTR. A Clinical TrialScott D Sagel, Umer Khan, Sonya L Heltshe, et al.
Pageof 8