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Claire L Keating

Showing results (1-10 of 9) with videos related to

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Chest|December 8, 2009
Classic respiratory disease but atypical diagnostic testing distinguishes adult presentation of cystic fibrosisClaire L Keating, Xinhua Liu, Emily A Dimango
Chest|May 22, 2021
Laryngeal Injury Due to Amikacin Inhalation for Refractory Mycobacterium avium Complex InfectionLucas G Axiotakis, Necati Enver, Claire L Keating, et al.
Chest|September 7, 2021
ResponseLucas G Axiotakis, Necati Enver, Claire L Keating, et al.
Annals of the American Thoracic Society|May 17, 2021
Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Advanced Cystic Fibrosis Lung DiseaseAmir Reza Djavid, Alison E Thompson, Alexandria L Irace, et al.
Antimicrobial Agents and Chemotherapy|December 15, 2020
<i>Pseudomonas aeruginosa</i> Susceptibility Patterns and Associated Clinical Outcomes in People with Cystic Fibrosis following Approval of Aztreonam Lysine for InhalationClaire L Keating, Jonathan B Zuckerman, Pradeep K Singh, et al.
International Journal of Telemedicine and Applications|March 17, 2021
Telerehabilitation Using Fitness Application in Patients with Severe Cystic Fibrosis Awaiting Lung Transplant: A Pilot StudyAimee M Layton, Andrew M Irwin, Erin C Mihalik, et al.
Bone|November 21, 2017
Adults with cystic fibrosis have deficits in bone structure and strength at the distal tibia despite similar size and measuring standard and relative sitesKyle K Nishiyama, Sanchita Agarwal, Anna Kepley, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 30, 2023
The gut microbiome, short chain fatty acids, and related metabolites in cystic fibrosis patients with and without colonic adenomasBrittany L Baldwin-Hunter, Felix D Rozenberg, Medini K Annavajhala, et al.
International Forum of Allergy & Rhinology|December 25, 2023
Determining the minimal clinically important difference for the questionnaire of olfactory disorders in people with cystic fibrosis and factors associated with improvement after highly effective modulator therapyJessa E Miller, Jennifer L Taylor-Cousar, Jonathan B Overdevest, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Chest|December 8, 2009
Classic respiratory disease but atypical diagnostic testing distinguishes adult presentation of cystic fibrosisClaire L Keating, Xinhua Liu, Emily A Dimango
Chest|May 22, 2021
Laryngeal Injury Due to Amikacin Inhalation for Refractory Mycobacterium avium Complex InfectionLucas G Axiotakis, Necati Enver, Claire L Keating, et al.
Chest|September 7, 2021
ResponseLucas G Axiotakis, Necati Enver, Claire L Keating, et al.
Annals of the American Thoracic Society|May 17, 2021
Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Advanced Cystic Fibrosis Lung DiseaseAmir Reza Djavid, Alison E Thompson, Alexandria L Irace, et al.
Antimicrobial Agents and Chemotherapy|December 15, 2020
<i>Pseudomonas aeruginosa</i> Susceptibility Patterns and Associated Clinical Outcomes in People with Cystic Fibrosis following Approval of Aztreonam Lysine for InhalationClaire L Keating, Jonathan B Zuckerman, Pradeep K Singh, et al.
International Journal of Telemedicine and Applications|March 17, 2021
Telerehabilitation Using Fitness Application in Patients with Severe Cystic Fibrosis Awaiting Lung Transplant: A Pilot StudyAimee M Layton, Andrew M Irwin, Erin C Mihalik, et al.
Bone|November 21, 2017
Adults with cystic fibrosis have deficits in bone structure and strength at the distal tibia despite similar size and measuring standard and relative sitesKyle K Nishiyama, Sanchita Agarwal, Anna Kepley, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 30, 2023
The gut microbiome, short chain fatty acids, and related metabolites in cystic fibrosis patients with and without colonic adenomasBrittany L Baldwin-Hunter, Felix D Rozenberg, Medini K Annavajhala, et al.
International Forum of Allergy & Rhinology|December 25, 2023
Determining the minimal clinically important difference for the questionnaire of olfactory disorders in people with cystic fibrosis and factors associated with improvement after highly effective modulator therapyJessa E Miller, Jennifer L Taylor-Cousar, Jonathan B Overdevest, et al.
Pageof 1