Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection

Risk factors for lung function decline in a large cohort of young cystic fibrosis patients

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Sputum Biomarkers of Inflammation and Lung Function Decline in Children with Cystic Fibrosis

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Persistent Methicillin-resistantStaphylococcus aureusand Rate of FEV1Decline in Cystic Fibrosis

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Interactions Between Secondhand Smoke and Genes That Affect Cystic Fibrosis Lung Disease

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Improvements in Lung Function Outcomes in Children with Cystic Fibrosis are Associated with Better Nutrition, Fewer Chronic Pseudomonas aeruginosa Infections, and Dornase Alfa Use

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Impact of Pseudomonas and Staphylococcus Infection on Inflammation and Clinical Status in Young Children with Cystic Fibrosis

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Genetic and non-genetic determinants of outcomes in cystic fibrosis

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Predictors of mucoidPseudomonas colonization in cystic fibrosis patients

(2008) Hara Levy et al.   PEDIATRIC PULMONOLOGY

The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosis

(2008) Gregory S. Sawicki et al.   PEDIATRIC PULMONOLOGY