Search research articles
Contact Us
Filters
Showing results (1-10 of 11) with videos related to
Page
of 2
Sort By:
Pediatric Clinics of North America
|
July 30, 2016
Respiratory System Disease
Danielle M Goetz, Shipra Singh
Pediatric Pulmonology
|
August 18, 2021
Review of CFTR modulators 2020
Danielle 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 report
Danielle M Goetz, Shipra Singh, Daniel Sheehan
Pediatric Pulmonology
|
June 27, 2020
Survey of patients with cystic fibrosis and caregivers decisions regarding CFTR modulators
Ashish 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 burden
Danielle M Goetz, Carla K Frederick, Geovanny Perez, et al.
Pediatric Pulmonology
|
January 8, 2010
Late presentation of congenital diaphragmatic hernia in patients with cystic fibrosis
Danielle 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 fibrosis
David 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 team
Rebekah 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 phenotypes
Denise 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 State
Hossein Sadeghi, Denise M Kay, Elinor Langfelder-Schwind, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Pediatric Clinics of North America
|
July 30, 2016
Respiratory System Disease
Danielle M Goetz, Shipra Singh
Pediatric Pulmonology
|
August 18, 2021
Review of CFTR modulators 2020
Danielle 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 report
Danielle M Goetz, Shipra Singh, Daniel Sheehan
Pediatric Pulmonology
|
June 27, 2020
Survey of patients with cystic fibrosis and caregivers decisions regarding CFTR modulators
Ashish 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 burden
Danielle M Goetz, Carla K Frederick, Geovanny Perez, et al.
Pediatric Pulmonology
|
January 8, 2010
Late presentation of congenital diaphragmatic hernia in patients with cystic fibrosis
Danielle 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 fibrosis
David 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 team
Rebekah 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 phenotypes
Denise 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 State
Hossein Sadeghi, Denise M Kay, Elinor Langfelder-Schwind, et al.
Page
of 2