Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: Analysis of the Cystic Fibrosis Foundation National CF Patient Registry

Journal of Pediatrics

Volumn 137, Issue 3, 2000, Pages 374-380

  Zemel, Babette S ^a,b,c   Jawad, Abbas F ^a,b,c   FitzSimmons, Stacey ^a,b,c   Stallings, Virginia A ^a,b,c  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

^c Pharmaceutical Research and Manufacturers of America   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; HUMAN; HUMAN CELL; HUMAN TISSUE; LUNG FUNCTION TEST; MAJOR CLINICAL STUDY; MALE; NUTRITIONAL STATUS; PANCREAS INSUFFICIENCY; PREPUBERTY; PRIORITY JOURNAL; SCORING SYSTEM; SEX DIFFERENCE;

EID: 0033827478     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2000.107891     Document Type: Article

References (25)

1. Relative underweight in cystic fibrosis and its prognostic value
2. Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption
3. Improved growth and clinical, nutritional and respiratory changes in response to nutritional therapy in cystic fibrosis
4. Short-term pulmonary effects of total parenteral nutrition in children with cystic fibrosis
5. Energy needs and nutritional rehabilitation in undernourished adolescents and adults with cystic fibrosis
6. Short-term clinical, nutritional, and functional effects of continuous elemental enteral alimentation in patients with cystic fibrosis
7. Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis
8. Nutritional rehabilitation in cystic fibrosis: Controlled studies of the effects on nutritional growth retardation, body protein turnover and cause of pulmonary disease
9. Nutritional rehabilitation in cystic fibrosis: A 5 year follow-up study
10. A comparison of survival, growth and pulmonary function in patients with cystic fibrosis in Boston and Toronto
11. Prediction of mortality in patients with cystic fibrosis
12. Stature as a prognostic factor in cystic fibrosis survival
13. Random-effects models for longitudinal data
14. Delayed puberty in girls with cystic fibrosis despite good clinical status
15. Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: Evaluation of various criteria used to identify malnutrition
16. Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis
17. The changing epidemiology of cystic fibrosis
18. Perspectives of longitudinal growth in cystic fibrosis from birth to adult age
19. Relationship between clinical parameters and linear growth in children with cystic fibrosis
20. Nutritional benefits of neonatal screening for cystic fibrosis
21. Growth patterns in children with cystic fibrosis
22. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis
23. Energy expenditure and genotype of children with cystic fibrosis