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Publications by David A. Waltz
Efficiency of Pulmonary Administration of Tobramycin Solution for Inhalation in Cystic Fibrosis Using an Improved Drug Delivery System
Chest
Cardiology
Critical Care
Cardiovascular Medicine
Intensive Care Medicine
Pulmonary
Respiratory Medicine
Nonproteolytic Role for the Urokinase Receptor in Cellular MigrationIn Vivo
American Journal of Respiratory Cell and Molecular Biology
Respiratory Medicine
Pulmonary
Clinical Biochemistry
Cell Biology
Molecular Biology
Related publications
Tobramycin Inhalation Powder in Cystic Fibrosis Patients: Response by Age Group
Respiratory Care
Medicine
Pulmonary
Critical Care
Respiratory Medicine
Intensive Care Medicine
Home Videos of Cystic Fibrosis Patients Using Tobramycin Inhalation Powder: Relation of Flow and Cough
Pediatric Pulmonology
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Safety, Efficacy and Convenience of Tobramycin Inhalation Powder in Cystic Fibrosis Patients: The EAGER Trial
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
PIN107 Tobramycin Inhaled Solution Utilization by Cystic Fibrosis Patients: An Analysis With the RAMQ Database
Value in Health
Medicine
Health Policy
Public Health
Occupational Health
Environmental
Bayesian Estimation of Tobramycin Exposure in Patients With Cystic Fibrosis
Antimicrobial Agents and Chemotherapy
Infectious Diseases
Pharmacology
Development of Levofloxacin Inhalation Solution to Treat Pseudomonas Aeruginosa in Patients With Cystic Fibrosis
Therapeutic Advances in Respiratory Disease
Pulmonary
Respiratory Medicine
Pharmacology
The Pharmacokinetics and Toxicity of Morning vs. Evening Tobramycin Dosing for Pulmonary Exacerbations of Cystic Fibrosis: A Randomised Comparison
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Treatment of Pulmonary Exacerbations of Cystic Fibrosis Leads to Improved Antioxidant Status
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
Pulmonary Nocardiosis in an Immunocompetent Patient With Cystic Fibrosis
Case Reports in Pulmonology