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Respiratory Care
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April 2, 2003
Neonatal and pediatric respiratory diagnostics
Stephanie D Davis
The New England Journal of Medicine
|
May 23, 2013
Identifying the origins of cystic fibrosis lung disease
Stephanie D Davis, Thomas Ferkol
American Journal of Respiratory and Critical Care Medicine
|
June 21, 2008
Reduced lung function in cystic fibrosis: a primary or secondary phenotype?
Stephanie D Davis, Felix Ratjen
Thorax
|
April 9, 2017
Preterm respiratory disease in the modern era: the value of cohort studies
Gregory S Montgomery, Stephanie D Davis
Pediatric Research
|
September 17, 2020
Challenges of academic pediatric medicine: the American Pediatric Society and Society for Pediatric Research Virtual Chat Series
Steven H Abman, Stephanie D Davis
The Journal of Pediatrics
|
November 9, 2015
Decline in Forced Expiratory Volume in 1 Second in Cystic Fibrosis--Watch the Pendulum Swing
Jessica E Pittman, Stephanie D Davis
Journal of Aerosol Medicine and Pulmonary Drug Delivery
|
January 31, 2014
Challenges and limitations of testing efficacy of aerosol device delivery in young children
Jennifer L Goralski, Stephanie D Davis
Chest
|
May 5, 2011
Infant pulmonary function testing: overview of technology and practical considerations--new current procedural terminology codes effective 2010
Burton L Lesnick, Stephanie D Davis
American Journal of Respiratory and Critical Care Medicine
|
December 17, 2010
Hitting the target: new treatments for cystic fibrosis
Stephanie D Davis, Thomas W Ferkol
Respiratory Medicine
|
July 12, 2014
Breathing easier: addressing the challenges of aerosolizing medications to infants and preschoolers
Jennifer L Goralski, Stephanie D Davis
Page
of 17
Search research articles
Search
Showing results (1-10 of 167) with videos related to
Sort By:
Page
of 17
Respiratory Care
|
April 2, 2003
Neonatal and pediatric respiratory diagnostics
Stephanie D Davis
The New England Journal of Medicine
|
May 23, 2013
Identifying the origins of cystic fibrosis lung disease
Stephanie D Davis, Thomas Ferkol
American Journal of Respiratory and Critical Care Medicine
|
June 21, 2008
Reduced lung function in cystic fibrosis: a primary or secondary phenotype?
Stephanie D Davis, Felix Ratjen
Thorax
|
April 9, 2017
Preterm respiratory disease in the modern era: the value of cohort studies
Gregory S Montgomery, Stephanie D Davis
Pediatric Research
|
September 17, 2020
Challenges of academic pediatric medicine: the American Pediatric Society and Society for Pediatric Research Virtual Chat Series
Steven H Abman, Stephanie D Davis
The Journal of Pediatrics
|
November 9, 2015
Decline in Forced Expiratory Volume in 1 Second in Cystic Fibrosis--Watch the Pendulum Swing
Jessica E Pittman, Stephanie D Davis
Journal of Aerosol Medicine and Pulmonary Drug Delivery
|
January 31, 2014
Challenges and limitations of testing efficacy of aerosol device delivery in young children
Jennifer L Goralski, Stephanie D Davis
Chest
|
May 5, 2011
Infant pulmonary function testing: overview of technology and practical considerations--new current procedural terminology codes effective 2010
Burton L Lesnick, Stephanie D Davis
American Journal of Respiratory and Critical Care Medicine
|
December 17, 2010
Hitting the target: new treatments for cystic fibrosis
Stephanie D Davis, Thomas W Ferkol
Respiratory Medicine
|
July 12, 2014
Breathing easier: addressing the challenges of aerosolizing medications to infants and preschoolers
Jennifer L Goralski, Stephanie D Davis
Page
of 17