James D. Acton

Tidal Breathing Responses to Albuterol and Normal Saline in Infants with Viral Bronchiolitis

Hyperplasia of pulmonary neuroendocrine cells in infancy and childhood

Cystic fibrosis

Nutritional immunity: transition metals at the pathogen–host interface

Augmented effect of early antibiotic treatment in mice with experimental lung infections due to sequentially adapted mucoid strains of Pseudomonas aeruginosa

Depressive symptoms in children with cystic fibrosis and parents and its effects on adherence to airway clearance

Nutrient Availability as a Mechanism for Selection of Antibiotic Tolerant Pseudomonas aeruginosa within the CF Airway

Lung clearance index: Evidence for use in clinical trials in cystic fibrosis

Longitudinal association between medication adherence and lung health in people with cystic fibrosis

European Cystic Fibrosis Society Standards of Care: Quality Management in cystic fibrosis

Antibiotic resistance of bacterial biofilms

Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience

A CFTR Potentiator in Patients with Cystic Fibrosis and the G551D Mutation

Pediatric Gastroesophageal Reflux Clinical Practice Guidelines: Joint Recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition (NASPGHAN) and the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN)

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

International Committee on Mental Health in Cystic Fibrosis: Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus statements for screening and treating depression and anxiety

Cystic fibrosis genetics: from molecular understanding to clinical application

Meta-Analysis of Psychological Interventions to Promote Adherence to Treatment in Pediatric Chronic Health Conditions

Comparison of two treatment regimens for eradication of Pseudomonas aeruginosa infection in children with cystic fibrosis

Innate immunity of the newborn: basic mechanisms and clinical correlates

Clinical practice and genetic counseling for cystic fibrosis and CFTR-related disorders

Update on Key Emerging Challenges in Cystic Fibrosis

Health Information Technology to Facilitate Communication Involving Health Care Providers, Caregivers, and Pediatric Patients: A Scoping Review

Cystic fibrosis and the role of gastrointestinal outcome measures in the new era of therapeutic CFTR modulation

Treatment of early Pseudomonas aeruginosa infection in patients with cystic fibrosis: the ELITE trial

Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling

Treatment of lung infection in patients with cystic fibrosis: Current and future strategies

Early Respiratory Infection Is Associated with Reduced Spirometry in Children with Cystic Fibrosis

SIDS and Other Sleep-Related Infant Deaths: Expansion of Recommendations for a Safe Infant Sleeping Environment

Pediatric Gastroesophageal Reflux Clinical Practice Guidelines

Clinical Practice Guideline: The Diagnosis, Management, and Prevention of Bronchiolitis

Hyperplasia and hypertrophy of pulmonary neuroepithelial bodies, presumed airway hypoxia sensors, in hypoxia-inducible factor prolyl hydroxylase-deficient mice

A scoping review of scoping reviews: advancing the approach and enhancing the consistency

Early Prediction of Severity in Acute Pancreatitis Using Infrared Spectroscopy of Serum

Cystic fibrosis: An update for clinicians. Part 1: Nutrition and gastrointestinal complications

Myeloperoxidase Promoter Polymorphism −463G Is Associated With More Severe Clinical Expression of Cystic Fibrosis Pulmonary Disease

Outcomes of fundoplication in children with cystic fibrosis

Case study: Providing evidence‐based behavioral and nutrition treatment to a toddler with cystic fibrosis and multiple food allergies via telehealth

Duration of treatment effect after tobramycin solution for inhalation in young children with cystic fibrosis

Neuroendocrine Cell Distribution and Frequency Distinguish Neuroendocrine Cell Hyperplasia of Infancy From Other Pulmonary Disorders

Multicenter Evaluation of Infant Lung Function Tests as Cystic Fibrosis Clinical Trial Endpoints

Improving Evidence-Based Care in Cystic Fibrosis Through Quality Improvement

Relations between depressive and anxious symptoms and quality of life in caregivers of children with cystic fibrosis

Fecal elastase-1: Utility in pancreatic function in cystic fibrosis

Phenotype of CF and the effects of possible modifier genes

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

Randomized Clinical Trial of Behavioral and Nutrition Treatment to Improve Energy Intake and Growth in Toddlers and Preschoolers With Cystic Fibrosis