There is no evidence of a primary defect in energy metabolism in subjects with cystic fibrosis

Journal of Pediatrics

Volumn 140, Issue 5, 2002, Pages 498-499

  Pencharz, Paul B ^a   Jackson, Reuben ^b  

^a UNIVERSITY OF TORONTO   (Canada)

^b HOSPITAL FOR SICK CHILDREN RESEARCH INSTITUTE   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BODY COMPOSITION; BODY SIZE; BODY WEIGHT; CALORIMETRY; CONTROLLED STUDY; CYSTIC FIBROSIS; EDITORIAL; ENERGY BALANCE; ENERGY EXPENDITURE; ENERGY METABOLISM; HUMAN; INFANT; LUNG FUNCTION; PRIORITY JOURNAL;

EID: 0036086048     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2002.124770     Document Type: Article

References (14)

1. Nutritional assessment and management in cystic fibrosis: A consensus report
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4. Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
5. Multi-ion pore behaviour in the CFTR chloride channel
6. Nucleoside triphosphates are required to open the CFTR chloride channel
7. Energy expenditure of patients with cystic fibrosis
8. Increased energy expenditure in cystic fibrosis associated with specific mutations
9. Increased energy expenditure in young children with cystic fibrosis
10. Energy expenditure in children with cystic fibrosis
11. Energy metabolism in infants with cystic fibrosis
12. Relationships of genetics, age, and physical fitness to daily energy expenditure and fuel utilization
13. Reexamination of the relationship of resting metabolic rate to fat-free mass and to the metabolically active components of fat-free mass in humans
14. Assessment of total energy expenditure in free-living patients with cystic fibrosis