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Stephanie D Davis

Showing results (41-50 of 167) with videos related to

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SAGE Open Medicine|November 1, 2017
Safety of intravenous tobramycin in combination with a variety of anti-pseudomonal antibiotics in children with cystic fibrosisAshley R Deschamp, Rebecca S Pettit, Jennifer A Donaldson, et al.
The Journal of Pediatrics|November 5, 2021
Trainee Characteristics, Subspecialty Choice, and Program Usage for the American Board of Pediatrics Resident Research Pathways, 2000-2019Adam L Turner, Colin J Orr, Stephanie D Davis, et al.
Pediatric Pulmonology|August 18, 2017
A comparison of nasal nitric oxide measurement modesAshley R Deschamp, Leah Schornick, Charles Clem, et al.
Pediatrics|August 7, 2013
Outcomes of children with severe bronchopulmonary dysplasia who were ventilator dependent at homeA Ioana Cristea, Aaron E Carroll, Stephanie D Davis, et al.
American Journal of Respiratory and Critical Care Medicine|June 26, 2013
Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical diseaseMichael R Knowles, Leigh Anne Daniels, Stephanie D Davis, et al.
Pediatric Pulmonology|September 2, 2021
Use caution interpreting nasal nitric oxide: Overlap in primary ciliary dyskinesia and primary immunodeficiencyAndrew T Barber, Stephanie D Davis, Hannah Boutros, et al.
American Journal of Respiratory and Critical Care Medicine|April 25, 2020
Limitations of Nasal Nitric Oxide Testing in Primary Ciliary DyskinesiaAdam J Shapiro, Stephanie D Davis, Margaret W Leigh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 3, 2014
Initial evaluation of the Parent Cystic Fibrosis Questionnaire--Revised (CFQ-R) in infants and young childrenAdrianne N Alpern, Lyndia C Brumback, Felix Ratjen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 12, 2025
Does using the Lung Clearance Index (LCI) inform clinical decisions in children with cystic fibrosis?Lucy Perrem, Stephanie Jeanneret-Manning, Stephanie D Davis, et al.
Journal of Medical Case Reports|July 30, 2013
A 2-year-old girl with co-inherited cystic fibrosis and sickle cell-β+ thalassemia presenting with recurrent vaso-occlusive events during cystic fibrosis pulmonary exacerbations: a case reportKurtis T Sobush, Courtney D Thornburg, Judith A Voynow, et al.
Pageof 17

Showing results (41-50 of 167) with videos related to

Sort By:
Pageof 17
SAGE Open Medicine|November 1, 2017
Safety of intravenous tobramycin in combination with a variety of anti-pseudomonal antibiotics in children with cystic fibrosisAshley R Deschamp, Rebecca S Pettit, Jennifer A Donaldson, et al.
The Journal of Pediatrics|November 5, 2021
Trainee Characteristics, Subspecialty Choice, and Program Usage for the American Board of Pediatrics Resident Research Pathways, 2000-2019Adam L Turner, Colin J Orr, Stephanie D Davis, et al.
Pediatric Pulmonology|August 18, 2017
A comparison of nasal nitric oxide measurement modesAshley R Deschamp, Leah Schornick, Charles Clem, et al.
Pediatrics|August 7, 2013
Outcomes of children with severe bronchopulmonary dysplasia who were ventilator dependent at homeA Ioana Cristea, Aaron E Carroll, Stephanie D Davis, et al.
American Journal of Respiratory and Critical Care Medicine|June 26, 2013
Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical diseaseMichael R Knowles, Leigh Anne Daniels, Stephanie D Davis, et al.
Pediatric Pulmonology|September 2, 2021
Use caution interpreting nasal nitric oxide: Overlap in primary ciliary dyskinesia and primary immunodeficiencyAndrew T Barber, Stephanie D Davis, Hannah Boutros, et al.
American Journal of Respiratory and Critical Care Medicine|April 25, 2020
Limitations of Nasal Nitric Oxide Testing in Primary Ciliary DyskinesiaAdam J Shapiro, Stephanie D Davis, Margaret W Leigh, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 3, 2014
Initial evaluation of the Parent Cystic Fibrosis Questionnaire--Revised (CFQ-R) in infants and young childrenAdrianne N Alpern, Lyndia C Brumback, Felix Ratjen, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 12, 2025
Does using the Lung Clearance Index (LCI) inform clinical decisions in children with cystic fibrosis?Lucy Perrem, Stephanie Jeanneret-Manning, Stephanie D Davis, et al.
Journal of Medical Case Reports|July 30, 2013
A 2-year-old girl with co-inherited cystic fibrosis and sickle cell-β+ thalassemia presenting with recurrent vaso-occlusive events during cystic fibrosis pulmonary exacerbations: a case reportKurtis T Sobush, Courtney D Thornburg, Judith A Voynow, et al.
Pageof 17