J. Wooldridge

发表

Changes in Pediatric Health-Related Quality of Life in Cystic Fibrosis After IV Antibiotic Treatment for Pulmonary Exacerbations

A. Quittner, K. Driscoll, A. Modi, 2010, Journal of Clinical Psychology in Medical Settings.

Using quality improvement science to implement a multidisciplinary behavioral intervention targeting pediatric inpatient airway clearance.

Karen M. Tucker, M. Seid, Karen M Tucker, 2010, Journal of pediatric psychology.

NO pathway in CF and non‐CF children

F. Accurso, P. Silkoff, S. Abman, 2004, Pediatric pulmonology.

Glucose tolerance, insulin secretion, and insulin sensitivity in children and adolescents with cystic fibrosis and no prior history of diabetes.

D. D’Alessio, L. Dolan, D. Elder, 2007, The Journal of pediatrics.

Persistent tachypnea and hypoxia in a 3-month-old term infant.

J. Whitsett, L. Young, G. Deutsch, 2006, The Journal of pediatrics.

Long-Term Experience With ZENPEP in Infants With Exocrine Pancreatic Insufficiency Associated With Cystic Fibrosis

R. Thieroff-Ekerdt, D. Jacobs, D. Schaeffer, 2014, Journal of pediatric gastroenterology and nutrition.

Parents' Religious Coping Styles in the First Year After Their Child's Cystic Fibrosis Diagnosis

Judith R. Ragsdale, D. Grossoehme, M. Seid, 2009, Journal of health care chaplaincy.

Enteral tube feeding for individuals with cystic fibrosis: Cystic Fibrosis Foundation evidence-informed guidelines.

S. Powers, S. Freedman, S. Schwarzenberg, 2016, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

EUR-1008 pancreatic enzyme replacement is safe and effective in patients with cystic fibrosis and pancreatic insufficiency.

K. Hardy, S. Boas, S. McColley, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

59 – Environmental Exposures in the Normal Host

R. Slavin, A. Knutsen, D. Bhatla, 2012 .

Effects of a PICU Status Asthmaticus De-Escalation Pathway on Length of Stay and Albuterol Use*

J. Wooldridge, L. Lowrie, S. Brennan, 2018, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

Transcriptional Adaptation to Cystic Fibrosis Transmembrane Conductance Regulator Deficiency*

B. Aronow, J. Whitsett, Yan Xu, 2003, The Journal of Biological Chemistry.

Insulin secretion abnormalities in exocrine pancreatic sufficient cystic fibrosis patients.

R. Szczesniak, M. Fenchel, D. Elder, 2015, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Improvements in Cystic Fibrosis Quarterly Visits, Lung Function Tests, and Respiratory Cultures

G. Albers, B. Noyes, J. Wooldridge, 2015, Pediatrics.

We Can Handle This: Parents' Use of Religion in the First Year Following Their Child's Diagnosis with Cystic Fibrosis

Judith R. Ragsdale, D. Grossoehme, M. Seid, 2009, Journal of health care chaplaincy.

Behavioral and nutritional treatment for preschool-aged children with cystic fibrosis: a randomized clinical trial.

R. Szczesniak, J. Clancy, S. Powers, 2015, JAMA pediatrics.

Behavioral and Nutritional Treatment for Preschool-Aged ChildrenWith Cystic Fibrosis

J. Clancy, J. Rausch, R. Castile, 2015 .

Aztreonam for inhalation solution (AZLI) in patients with cystic fibrosis, mild lung impairment, and P. aeruginosa.

R. Gibson, S. Lewis, A. Quittner, 2011, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Diaphragmatic hernia simulating a left pleural effusion.

R. Deterding, D. Partrick, D. Bensard, 2003, Pediatrics.