Cystic Fibrosis Upper Airways Primary Colonization withPseudomonas aeruginosa: Eradicated by Sinonasal Antibiotic Inhalation
Author:
Publisher
American Thoracic Society
Subject
Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine
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1. Adaptation and genomic erosion in fragmented Pseudomonas aeruginosa populations in the sinuses of people with cystic fibrosis;Cell Reports;2021-10
2. Ivacaftor Reduces Inflammatory Mediators in Upper Airway Lining Fluid From Cystic Fibrosis Patients With a G551D Mutation: Serial Non-Invasive Home-Based Collection of Upper Airway Lining Fluid;Frontiers in Immunology;2021-05-05
3. Evolution and adaptation ofPseudomonas aeruginosain the paranasal sinuses of people with cystic fibrosis;2020-10-29
4. Longitudinal monitoring of sinonasal and oral bacterial reservoirs to prevent chronic lung infection in people with cystic fibrosis;ERJ Open Research;2020-07
5. Chronic rhino-sinusitis treatment in children with cystic fibrosis: A cross-sectional survey of pediatric pulmonologists and otolaryngologists;International Journal of Pediatric Otorhinolaryngology;2019-09
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