Stephanie D. Davis, M.D.
Affiliations: | 2011-2018 | Pediatric Pulmonology | Riley Hospital for Children, Indianapolis, Xinjiang, China |
| 2018- | Pediatrics | University of North Carolina, Chapel Hill, Chapel Hill, NC |
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"Stephanie Davis"Parents
Sign in to add mentor| Jennifer L. Wiebke | fellowship/program director | 1996-1999 | Riley Hospital for Children |
Children
Sign in to add trainee| Ceila E. Loughlin | fellowship/program director | 2008 | UNC Chapel Hill |
| Stacey Peterson-Carmichael | fellowship/program director | 2004-2008 | UNC Chapel Hill |
| Chandar Ramanathan | fellowship/program director | 2007-2010 | UNC Chapel Hill |
| Kavita Patel | fellowship/program director | 2011 | UNC Chapel Hill |
| Jessica Pittman | fellowship/program director | 2011 | UNC Chapel Hill |
| Adam J. Shapiro | fellowship/program director | 2011 | UNC Chapel Hill |
| Drew Barber | research mentor | University of North Carolina-Chapel Hill |
Collaborators
Sign in to add collaborator| Felix Ratjen | collaborator | ||
| Clement Ren | collaborator | ||
| Margaret Rosenfeld | collaborator |
BETA: Related publications
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Publications
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| Kinghorn B, Rosenfeld M, Sullivan E, et al. (2024) Comparison of Longitudinal Outcomes in Children with Primary Ciliary Dyskinesia and Cystic Fibrosis. Annals of the American Thoracic Society |
| Kaspy KR, Dell SD, Davis SD, et al. (2023) Situs ambiguus is associated with adverse clinical outcomes in children with primary ciliary dyskinesia. Chest |
| DeBoer EM, Morgan WJ, Quiros-Alcala L, et al. (2023) Defining and Promoting Pediatric Pulmonary Health: Assessing Lung Function and Structure. Pediatrics. 152 |
| Chen Y, Lv Q, Andrinopoulou ER, et al. (2023) Automatic bronchus and artery analysis on chest computed tomography to evaluate the effect of inhaled hypertonic saline in children aged 3-6 years with cystic fibrosis in a randomized clinical trial. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society |
| Kinghorn B, Rosenfeld M, Sullivan E, et al. (2022) Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype. Annals of the American Thoracic Society |
| Barber AT, Shapiro AJ, Davis SD, et al. (2022) Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype. Annals of the American Thoracic Society |
| Sagel SD, Kupfer O, Wagner BD, et al. (2022) Airway Inflammation in Children with Primary Ciliary Dyskinesia. Annals of the American Thoracic Society |
| Perrem L, Stanojevic S, Shaw M, et al. (2022) Comparative analysis of respiratory symptom scores to detect acute respiratory events in children with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society |
| Wee WB, Leigh MW, Davis SD, et al. (2022) Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia. Annals of the American Thoracic Society |
| Sanders DB, Deschamp AR, Hatch JE, et al. (2022) Association between early respiratory viral infections and structural lung disease in infants with cystic fibrosis. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society |