Growth and nutritional indexes in early life predict pulmonary function in cystic fibrosis
Authors:
- Michael W. KonstanMKMichael W. Konstan
- Steven M. ButlerSBSteven M. Butler
- Mary Ellen B. WohlMWMary Ellen B. Wohl
- Marcia StoddardMSMarcia Stoddard
- Robert MatousekRMRobert Matousek
- Jeffrey S. WagenerJWJeffrey S. Wagener
- Charles A. JohnsonCJCharles A. Johnson
- Wayne J. MorganWMWayne J. Morgan
- 1 June 2003
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 142 (6) , 624-630
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- “Ethnic” variation in childhood lung function may relate to preventable nutritional deficiencyActa Paediatrica, 2001
- Early Diagnosis of Cystic Fibrosis Through Neonatal Screening Prevents Severe Malnutrition and Improves Long-Term GrowthPediatrics, 2001
- Long term prognosis of patients with cystic fibrosis in relation to early detection by neonatal screening and treatment in a cystic fibrosis centre.Thorax, 1995
- Effect of High-Dose Ibuprofen in Patients with Cystic FibrosisNew England Journal of Medicine, 1995
- Pulmonary function between 6 and 18 years of agePediatric Pulmonology, 1993
- The cystic fibrosis gene and resting energy expenditureThe Journal of Pediatrics, 1991
- A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and TorontoJournal of Clinical Epidemiology, 1988
- Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorptionThe Journal of Pediatrics, 1982
- Improved growth and clinical, nutritional, and respiratory changes in response to nutritional therapy in cystic fibrosisThe Journal of Pediatrics, 1980
- Lung function of healthy boys and girls in Jamaica in relation to ethnic composition, test exercise performance, and habitual physical activityThorax, 1977