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Pediatric Pulmonology|June 17, 2022
Defining and identifying early-onset lung disease in cystic fibrosis with cumulative clinical characteristicsLeslie Huang, HuiChuan J Lai, Nicholas Antos, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 18, 2020
Newborn screening alone insufficient to improve pulmonary outcomes for cystic fibrosisChristina B Barreda, Philip M Farrell, Anita Laxova, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|May 15, 2013
Health-related quality of life in children and adolescents with cystic fibrosis: convergent validity with parent-reports and objective measures of pulmonary healthAudrey Tluczek, Tara Becker, Adam Grieve, et al.Annals of the American Thoracic Society|August 9, 2018
Tidal Breathing Measurements at Discharge and Clinical Outcomes in Extremely Low Gestational Age NeonatesClement L Ren, Rui Feng, Stephanie D Davis, et al.Pediatric Pulmonology|December 14, 2011
Regional differences in the evolution of lung disease in children with cystic fibrosisZhanhai Li, Don B Sanders, Michael J Rock, et al.JAMA|June 8, 2002
Respiratory infections with Pseudomonas aeruginosa in children with cystic fibrosis: early detection by serology and assessment of risk factorsSusan E H West, Lan Zeng, Bee Leng Lee, et al.Life (Basel, Switzerland)|February 11, 2021
F1099L-CFTR (c.3297C>G) has Impaired Channel Function and Associates with Mild Disease Phenotypes in Two Pediatric PatientsXiaoying Zhang, Jaspal S Hothi, Yanhui H Zhang, et al.American Journal of Respiratory and Critical Care Medicine|August 15, 2003
Bronchopulmonary disease in children with cystic fibrosis after early or delayed diagnosisPhilip M Farrell, Zhanhai Li, Michael R Kosorok, et al.Chest|November 26, 2010
Relationships among health-related quality of life, pulmonary health, and newborn screening for cystic fibrosisAudrey Tluczek, Tara Becker, Anita Laxova, et al.Radiology|August 26, 2009
Association between mucoid Pseudomonas infection and bronchiectasis in children with cystic fibrosisPhilip M Farrell, Jannette Collins, Lynn S Broderick, et al.Pageof 5