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Edith T Zemanick

Showing results (51-60 of 89) with videos related to

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Frontiers in Medicine|January 26, 2023
Using metabolic potential within the airway microbiome as predictors of clinical state in persons with cystic fibrosisGabriella Shumyatsky, Aszia Burrell, Hollis Chaney, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|May 22, 2021
Importance of beta-lactam pharmacokinetics and pharmacodynamics on the recovery of microbial diversity in the airway of persons with cystic fibrosisAndrea Hahn, Aszia Burrell, Hollis Chaney, et al.
Pediatric Pulmonology|September 24, 2020
Oral antibiotic prescribing patterns for treatment of pulmonary exacerbations in two large pediatric CF centersJordana E Hoppe, Daniel M Hinds, Adrianne Colborg, et al.
Frontiers in Microbiology|June 7, 2018
On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial CommunitiesBrandie D Wagner, Gary K Grunwald, Gary O Zerbe, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 19, 2023
Olfactory loss in people with cystic fibrosis: Community perceptions and impactJessa E Miller, Christine M Liu, Edith T Zemanick, et al.
Pediatric Pulmonology|April 17, 2018
Highlights from the 2017 North American Cystic Fibrosis ConferenceStacey L Martiniano, Demet Toprak, Thida Ong, et al.
The Pediatric Infectious Disease Journal|July 16, 2021
Impact of Anaerobic Antibacterial Spectrum on Cystic Fibrosis Airway Microbiome Diversity and Pulmonary FunctionMichael J Bozzella, Hollis Chaney, Iman Sami, et al.
Proteomics. Clinical Applications|November 16, 2018
Novel Application of Aptamer Proteomic Analysis in Cystic Fibrosis Bronchoalveolar Lavage FluidEmily M DeBoer, Brandie D Wagner, Jonathan Popler, et al.
Annals of the American Thoracic Society|October 12, 2019
Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D MutationJ Kirk Harris, Brandie D Wagner, Edith T Zemanick, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 12, 2021
Measuring the impact of CFTR modulation on sweat chloride in cystic fibrosis: Rationale and design of the CHEC-SC studyEdith T Zemanick, Michael W Konstan, Donald R VanDevanter, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Frontiers in Medicine|January 26, 2023
Using metabolic potential within the airway microbiome as predictors of clinical state in persons with cystic fibrosisGabriella Shumyatsky, Aszia Burrell, Hollis Chaney, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|May 22, 2021
Importance of beta-lactam pharmacokinetics and pharmacodynamics on the recovery of microbial diversity in the airway of persons with cystic fibrosisAndrea Hahn, Aszia Burrell, Hollis Chaney, et al.
Pediatric Pulmonology|September 24, 2020
Oral antibiotic prescribing patterns for treatment of pulmonary exacerbations in two large pediatric CF centersJordana E Hoppe, Daniel M Hinds, Adrianne Colborg, et al.
Frontiers in Microbiology|June 7, 2018
On the Use of Diversity Measures in Longitudinal Sequencing Studies of Microbial CommunitiesBrandie D Wagner, Gary K Grunwald, Gary O Zerbe, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 19, 2023
Olfactory loss in people with cystic fibrosis: Community perceptions and impactJessa E Miller, Christine M Liu, Edith T Zemanick, et al.
Pediatric Pulmonology|April 17, 2018
Highlights from the 2017 North American Cystic Fibrosis ConferenceStacey L Martiniano, Demet Toprak, Thida Ong, et al.
The Pediatric Infectious Disease Journal|July 16, 2021
Impact of Anaerobic Antibacterial Spectrum on Cystic Fibrosis Airway Microbiome Diversity and Pulmonary FunctionMichael J Bozzella, Hollis Chaney, Iman Sami, et al.
Proteomics. Clinical Applications|November 16, 2018
Novel Application of Aptamer Proteomic Analysis in Cystic Fibrosis Bronchoalveolar Lavage FluidEmily M DeBoer, Brandie D Wagner, Jonathan Popler, et al.
Annals of the American Thoracic Society|October 12, 2019
Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D MutationJ Kirk Harris, Brandie D Wagner, Edith T Zemanick, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|February 12, 2021
Measuring the impact of CFTR modulation on sweat chloride in cystic fibrosis: Rationale and design of the CHEC-SC studyEdith T Zemanick, Michael W Konstan, Donald R VanDevanter, et al.
Pageof 9