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Danielle M Goetz

Showing results (1-10 of 11) with videos related to

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Pediatric Clinics of North America|July 30, 2016
Respiratory System DiseaseDanielle M Goetz, Shipra Singh
Pediatric Pulmonology|August 18, 2021
Review of CFTR modulators 2020Danielle M Goetz, Adrienne P Savant
Respiratory Medicine Case Reports|January 9, 2016
Effect of enterovirus D68 on Lung Clearance Index in patients with cystic fibrosis: A case reportDanielle M Goetz, Shipra Singh, Daniel Sheehan
Pediatric Pulmonology|June 27, 2020
Survey of patients with cystic fibrosis and caregivers decisions regarding CFTR modulatorsAshish George, Beth Smith, Gregory S Sawicki, et al.
Pediatric Pulmonology|May 26, 2023
Airway clearance after highly effective CFTR modulators: Normalizing life and reducing treatment burdenDanielle M Goetz, Carla K Frederick, Geovanny Perez, et al.
Pediatric Pulmonology|January 8, 2010
Late presentation of congenital diaphragmatic hernia in patients with cystic fibrosisDanielle M Goetz, Cartland Burns, Bradley J Segura, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 26, 2023
Airway clearance therapy in the school environment: Retrospective analysis of a cohort of pediatric patients with cystic fibrosisDavid J Byrwa, Geovanny F Perez, Christine M Roach, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 26, 2024
Cystic fibrosis foundation position paper: Redefining the cystic fibrosis care teamRebekah F Brown, Charlotte T Close, Molly G Mailes, et al.
Pediatric Pulmonology|May 2, 2024
Genetic counseling access and service delivery in New York State is variable for parents of infants with complex CFTR genotypes conferring uncertain phenotypesDenise M Kay, Hossein Sadeghi, Catherine Kier, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 12, 2024
Characterization of 223 infants with CFTR-related metabolic syndrome/Cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID) identified during the first three years of newborn screening via IRT-DNA-SEQ in New York StateHossein Sadeghi, Denise M Kay, Elinor Langfelder-Schwind, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatric Clinics of North America|July 30, 2016
Respiratory System DiseaseDanielle M Goetz, Shipra Singh
Pediatric Pulmonology|August 18, 2021
Review of CFTR modulators 2020Danielle M Goetz, Adrienne P Savant
Respiratory Medicine Case Reports|January 9, 2016
Effect of enterovirus D68 on Lung Clearance Index in patients with cystic fibrosis: A case reportDanielle M Goetz, Shipra Singh, Daniel Sheehan
Pediatric Pulmonology|June 27, 2020
Survey of patients with cystic fibrosis and caregivers decisions regarding CFTR modulatorsAshish George, Beth Smith, Gregory S Sawicki, et al.
Pediatric Pulmonology|May 26, 2023
Airway clearance after highly effective CFTR modulators: Normalizing life and reducing treatment burdenDanielle M Goetz, Carla K Frederick, Geovanny Perez, et al.
Pediatric Pulmonology|January 8, 2010
Late presentation of congenital diaphragmatic hernia in patients with cystic fibrosisDanielle M Goetz, Cartland Burns, Bradley J Segura, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 26, 2023
Airway clearance therapy in the school environment: Retrospective analysis of a cohort of pediatric patients with cystic fibrosisDavid J Byrwa, Geovanny F Perez, Christine M Roach, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 26, 2024
Cystic fibrosis foundation position paper: Redefining the cystic fibrosis care teamRebekah F Brown, Charlotte T Close, Molly G Mailes, et al.
Pediatric Pulmonology|May 2, 2024
Genetic counseling access and service delivery in New York State is variable for parents of infants with complex CFTR genotypes conferring uncertain phenotypesDenise M Kay, Hossein Sadeghi, Catherine Kier, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 12, 2024
Characterization of 223 infants with CFTR-related metabolic syndrome/Cystic fibrosis screen positive, inconclusive diagnosis (CRMS/CFSPID) identified during the first three years of newborn screening via IRT-DNA-SEQ in New York StateHossein Sadeghi, Denise M Kay, Elinor Langfelder-Schwind, et al.
Pageof 2