Stephanie D Davis

Summary

Affiliation: University of North Carolina
Country: USA

Publications

  1. pmc Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints
    Stephanie D Davis
    Department of Pediatrics, North Carolina Children s Hospital, University of North Carolina at Chapel Hill, USA
    Am J Respir Crit Care Med 182:1387-97. 2010
  2. ncbi request reprint Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis
    Stephanie D Davis
    Division of Pediatric Pulmonology, Chapel Hill, NC 27599 7220, USA
    Am J Respir Crit Care Med 175:943-50. 2007
  3. pmc Endpoints for clinical trials in young children with cystic fibrosis
    Stephanie D Davis
    Division of Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
    Proc Am Thorac Soc 4:418-30. 2007
  4. pmc Exhaled breath condensate purines correlate with lung function in infants and preschoolers
    Kavita Patel
    Department of Pediatric Pulmonology, University of North Carolina, Chapel Hill, North Carolina, USA
    Pediatr Pulmonol 48:182-7. 2013
  5. doi request reprint Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis
    Stacey L Peterson-Carmichael
    Division of Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
    Pediatr Pulmonol 44:503-11. 2009
  6. pmc Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia
    M Leigh Anne Daniels
    Department of Medicine, UNC School of Medicine, Chapel Hill, North Carolina
    Hum Mutat 34:1352-6. 2013
  7. pmc Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
    Michael R Knowles
    University of North Carolina, Cystic Fibrosis Pulmonary Research and Treatment Center, School of Medicine, CB 7248, 7123 Thurston Bowles Bldg, Chapel Hill, NC 27599 7248, USA
    Thorax 67:433-41. 2012
  8. pmc Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
    Michael R Knowles
    Department of Medicine, UNC School of Medicine, Chapel Hill, NC 27599, USA
    Am J Hum Genet 92:99-106. 2013
  9. doi request reprint Variability of a closed, rebreathing setup for multiple breath wash-out testing in children
    Jessica E Pittman
    Division of Pediatric Pulmonology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    Pediatr Pulmonol 47:1242-50. 2012
  10. ncbi request reprint Improvement in pulmonary function following antibiotics in infants with cystic fibrosis
    Jessica E Pittman
    Division of Pediatric Pulmonology, University of North Carolina at Chapel Hill, 130 Mason Farm Road, Chapel Hill, NC 27599, USA
    Pediatr Pulmonol 47:441-6. 2012

Detail Information

Publications19

  1. pmc Multicenter evaluation of infant lung function tests as cystic fibrosis clinical trial endpoints
    Stephanie D Davis
    Department of Pediatrics, North Carolina Children s Hospital, University of North Carolina at Chapel Hill, USA
    Am J Respir Crit Care Med 182:1387-97. 2010
    ..The conducting of clinical trials in infants with cystic fibrosis (CF) has been hindered by lack of sensitive outcome measures...
  2. ncbi request reprint Computed tomography reflects lower airway inflammation and tracks changes in early cystic fibrosis
    Stephanie D Davis
    Division of Pediatric Pulmonology, Chapel Hill, NC 27599 7220, USA
    Am J Respir Crit Care Med 175:943-50. 2007
    ..Detecting and tracking early cystic fibrosis (CF) lung disease are difficult due to lack of sensitive markers of airway dysfunction...
  3. pmc Endpoints for clinical trials in young children with cystic fibrosis
    Stephanie D Davis
    Division of Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
    Proc Am Thorac Soc 4:418-30. 2007
    ..Further development of these outcomes measures will enable clinical trials in the youngest CF population with the objective of improving long-term prognosis...
  4. pmc Exhaled breath condensate purines correlate with lung function in infants and preschoolers
    Kavita Patel
    Department of Pediatric Pulmonology, University of North Carolina, Chapel Hill, North Carolina, USA
    Pediatr Pulmonol 48:182-7. 2013
    ..Measurement of exhaled breath condensate (EBC) purines and other biomarkers offers a less invasive method to assess airway inflammation; however, the feasibility and utility of EBC biomarkers in young children has not been established...
  5. doi request reprint Association of lower airway inflammation with physiologic findings in young children with cystic fibrosis
    Stacey L Peterson-Carmichael
    Division of Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
    Pediatr Pulmonol 44:503-11. 2009
    ....
  6. pmc Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia
    M Leigh Anne Daniels
    Department of Medicine, UNC School of Medicine, Chapel Hill, North Carolina
    Hum Mutat 34:1352-6. 2013
    ..921+3_6delAAGT splice-site mutation in RSPH4A were Hispanic with ancestry tracing to Puerto Rico. This mutation is a founder mutation and a common cause of PCD without situs abnormalities in patients of Puerto Rican descent. ..
  7. pmc Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
    Michael R Knowles
    University of North Carolina, Cystic Fibrosis Pulmonary Research and Treatment Center, School of Medicine, CB 7248, 7123 Thurston Bowles Bldg, Chapel Hill, NC 27599 7248, USA
    Thorax 67:433-41. 2012
    ....
  8. pmc Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
    Michael R Knowles
    Department of Medicine, UNC School of Medicine, Chapel Hill, NC 27599, USA
    Am J Hum Genet 92:99-106. 2013
    ..These results revealed that mutations in CCDC114 are a cause of ciliary dysmotility and PCD and further demonstrate the utility of exome sequencing to identify genetic causes in heterogeneous recessive disorders...
  9. doi request reprint Variability of a closed, rebreathing setup for multiple breath wash-out testing in children
    Jessica E Pittman
    Division of Pediatric Pulmonology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA
    Pediatr Pulmonol 47:1242-50. 2012
    ..S. Our objective was to assess validity and sensitivity of a commercially available device that uses a closed (rebreathing) setup with photoacoustic spectroscopy for MBW testing...
  10. ncbi request reprint Improvement in pulmonary function following antibiotics in infants with cystic fibrosis
    Jessica E Pittman
    Division of Pediatric Pulmonology, University of North Carolina at Chapel Hill, 130 Mason Farm Road, Chapel Hill, NC 27599, USA
    Pediatr Pulmonol 47:441-6. 2012
    ..While pulmonary function testing (PFT) is often used to follow progression of lung disease and guide treatment in older children with CF, little data is available on change in infant PFTs in young children with CF...
  11. ncbi request reprint Physiologic, bronchoscopic, and bronchoalveolar lavage fluid findings in young children with recurrent wheeze and cough
    John Saito
    Division of Pulmonology, Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599 7220, USA
    Pediatr Pulmonol 41:709-19. 2006
    ....
  12. pmc Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
    Margaret W Leigh
    Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA
    Genet Med 11:473-87. 2009
    ....
  13. doi request reprint Early lung disease in young children with primary ciliary dyskinesia
    David E Brown
    Department of Pediatrics, Division of Pulmonology, University of North Carolina, Chapel Hill, North Carolina, USA
    Pediatr Pulmonol 43:514-6. 2008
    ..We report on 3 young children with PCD who had evidence of lung disease on infant pulmonary function testing, bronchoscopy, and/or computed tomography (CT) of the chest before 3 years of age...
  14. doi request reprint Safety and tolerability of inhaled hypertonic saline in young children with cystic fibrosis
    Elisabeth P Dellon
    Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599 7217, USA
    Pediatr Pulmonol 43:1100-6. 2008
    ..Initiating therapies in young patients has potential to preserve lung function. Before conducting a therapeutic trial of HS in this population, its safety must be evaluated and protocols for monitoring response must be tested...
  15. pmc Eosinophilic esophagitis in cystic fibrosis: a case series and review of the literature
    Jennifer L Goralski
    Division of Pediatric Pulmonology, Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC, United States
    J Cyst Fibros 12:9-14. 2013
    ..We present three patients with CF diagnosed with EoE and review the current literature regarding diagnosis and management, focusing on management issues in patients with CF...
  16. ncbi request reprint Quality of pulmonary function testing in 3 large primary care pediatric clinics in rural North Carolina
    Chris Gillette
    Eshelman School of Pharmacy, University of North Carolina Chapel Hill, Chapel Hill, NC 27599, USA
    N C Med J 72:105-10. 2011
    ..Pulmonary function testing (eg, spirometry) is recommended by the National Heart, Lung, and Blood Institute as part of basic asthma management. Previous research has shown that spirometry is feasible in primary care settings...
  17. ncbi request reprint Neonatal and pediatric respiratory diagnostics
    Stephanie D Davis
    Department of Pediatrics, University of North Carolina at Chapel Hill, 27599 7220, USA
    Respir Care 48:367-84; discussion 384-5. 2003
    ..These remarkable advances have yet to be applied in multicenter trials with young children. Adhering to standards will be critical for future multicenter trials to assess the clinical utility of these potential outcome measures...
  18. ncbi request reprint Reduced lung function in cystic fibrosis: a primary or secondary phenotype?
    Stephanie D Davis
    Am J Respir Crit Care Med 178:2-3. 2008
  19. ncbi request reprint An official American Thoracic Society/European Respiratory Society statement: pulmonary function testing in preschool children
    Nicole Beydon
    Am J Respir Crit Care Med 175:1304-45. 2007