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  • Sarah M Varekojis, Françoise Douce, +4 authors Robert G. Castile
  • Medicine
  • Respiratory care
  • 2003
  • INTRODUCTION Cystic fibrosis (CF) patients have abnormally viscid bronchial secretions that cause airway obstruction, inflammation, and infection that leads to lung damage. To enhance airwayContinue Reading
  • Kathryn S. Mueller, Frederick R. Long, Robert L Flucke, Robert G. Castile
  • Medicine
  • Pediatric Radiology
  • 2010 (First Publication: 1 October 2010)
  • BackgroundLung inflation and respiratory motion during chest CT affect diagnostic accuracy and reproducibility.ObjectiveTo describe a simple volume-monitored (VM) method for performing reproducible,Continue Reading
  • Karen S Mccoy, Robert G. Castile, Elizabeth D. Allen, David A Filbrun, Robert L Flucke, Ephraim Bar-Yishay
  • Medicine
  • Pediatric pulmonology
  • 1995 (First Publication: 1 May 1995)
  • Comparative measurements of functional residual capacity (FRC) made by plethysmography (FRCpleth) and by helium dilution (FRCHe) were obtained on 27 infants and young children without known pulmonaryContinue Reading
  • Shahid I. Sheikh, Frederick R. Long, Robert L Flucke, Nancy A. Ryan-Wenger, Don Hayes, Karen S Mccoy
  • Medicine
  • Lung
  • 2015 (First Publication: 1 June 2015)
  • BackgroundInfants with cystic fibrosis (CF) develop early progressive lung disease which may be asymptomatic. Infant pulmonary function tests (IPFT) and controlled ventilation-high resolutionContinue Reading