Conditions Associated with the Cystic Fibrosis Defect Promote ChronicPseudomonas aeruginosaInfection

The in vivo biofilm

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Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung

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Infection, Inflammation, and Lung Function Decline in Infants with Cystic Fibrosis

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Comparative Efficacy and Safety of 4 Randomized Regimens to Treat Early Pseudomonas aeruginosa Infection in Children With Cystic Fibrosis

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Initial Pseudomonas aeruginosa infection in patients with cystic fibrosis: characteristics of eradicated and persistent isolates

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Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection

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Phenotypes of Non-Attached Pseudomonas aeruginosa Aggregates Resemble Surface Attached Biofilm

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Active Starvation Responses Mediate Antibiotic Tolerance in Biofilms and Nutrient-Limited Bacteria

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The Pel Polysaccharide Can Serve a Structural and Protective Role in the Biofilm Matrix of Pseudomonas aeruginosa

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Pseudomonas aeruginosa Cystic Fibrosis isolates of similar RAPD genotype exhibit diversity in biofilm forming ability in vitro

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Biofilm Formation Enhances the Oxygen Tolerance and Invasiveness ofFusobacterium nucleatumin an Oral Mucosa Culture Model

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Delayed wound healing in diabetic (db/db) mice with Pseudomonas aeruginosa biofilm challenge: a model for the study of chronic wounds

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Azithromycin Maintains Airway Epithelial Integrity duringPseudomonas aeruginosaInfection

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Immunodeficiencies

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Instantaneous Within-Patient Diversity of Pseudomonas aeruginosa Quorum-Sensing Populations from Cystic Fibrosis Lung Infections

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Biofilm-forming Pseudomonas aeruginosa bacteria undergo lipopolysaccharide structural modifications and induce enhanced inflammatory cytokine response in human monocytes

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Pseudomonas aeruginosabiofilms in the respiratory tract of cystic fibrosis patients

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Relationship between antimicrobial proteins and airway inflammation and infection in cystic fibrosis

(2009) Scott D. Sagel et al.   PEDIATRIC PULMONOLOGY

The role of chloride anion and CFTR in killing of Pseudomonas aeruginosa by normal and CF neutrophils

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Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis

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Physiological heterogeneity in biofilms

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