Cystic fibrosis: Nutritional considerations;Fibrosis quística: Aspectos nutricionales

Anales Espanoles de Pediatria

Volumn 54, Issue 6, 2001, Pages 575-581

  Molina Arias, M ^a   Prieto Bozano, G ^a   Sarria Oses J ^a   Polanco Allue I ^a  

^a HOSPITAL INFANTIL LA PAZ   (Spain)

Author keywords

Cystic fibrosis; Energy balance; Malnutrition; Nutritional support

Indexed keywords

CARBOHYDRATE; FAT; PROTEIN; VITAMIN;

ANTHROPOMETRY; ARTICLE; CALORIC INTAKE; CYSTIC FIBROSIS; ENERGY BALANCE; ENERGY EXPENDITURE; FAT INTAKE; HUMAN; MALNUTRITION; NUTRITIONAL STATUS; NUTRITIONAL SUPPORT; PANCREAS INSUFFICIENCY; PROTEIN INTAKE; QUALITY OF LIFE; RESPIRATORY FUNCTION; VITAMIN SUPPLEMENTATION;

CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; HUMANS; INFANT; INFANT, NEWBORN; NUTRITION DISORDERS; NUTRITIONAL STATUS; SURVIVAL RATE;

EID: 0035745435     PISSN: 03024342     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (39)

1. Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis
2. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: Analysis of the Cystic Fibrosis Foundation National CF Patient Registry
3. Prediction of mortality in patients with cystic fibrosis
4. Nutrition and survival in cystic fibrosis
5. The pathogenesis of wasting in AIDS: Lessons for cystic fibrosis
6. Plasma vitamin C concentrations in patients with cystic fibrosis: Evidence of associations with lung inflammation
7. Cystic fibrosis
8. Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: Evaluation of various criteria used to identify malnutrition
9. Perspectives of longitudinal growth in cystic fibrosis from birth to adult age
10. Relationship between clinical parameters and linear growth in children with cystic fibrosis
11. Nutritional status of children with cystic fibrosis measured by total body potassium as a marker of body cell mass: Lack of sensitivity of anthropometric measures
12. Relation between dietary intake and nutritional status in cystic fibrosis
13. Longitudinal, prospective analysis of dietary intake in children with cystic fibrosis
14. Malnutrition in children with cystic fibrosis: The energy-balance equation
15. Effect of elective antibiotic therapy on resting energy expenditure and inflammation in cystic fibrosis
16. Energy balance during acute respiratory exacerbations in children with cystic fibrosis
17. Resting energy expenditure, pulmonary inflammation, and genotype in the early course of cystic fibrosis
18. Energy expenditure and substrate utilization in adults with cystic fibrosis and diabetes mellitus
19. Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis
20. Structure and function of the CFTR chloride channel
21. Nutritional status of patients with cystic fibrosis with meconium ileus: A comparison with patients without meconium ileus and diagnosed early through neonatal screening
22. Nutritional management of cystic fibrosis
23. Tratamiento dietético
24. Growth of human milk-fed and formula-fed infants with cystic fibrosis
25. Do infants with cystic fibrosis need a protein hydrosylate formula? A prospective, randomized, comparative study
26. Enteral nutrition for patients with cystic fibrosis: Comparison of a semi-elemental and nonelemental formula
27. Challenges in the dietary treatment of cystic fibrosis related diabetes mellitus
28. Role of polyunsaturated fatty acids in lung disease
29. - mice
30. Vitamin A status in acute exacerbations of cystic fibrosis
31. Bone mineral content in cystic fibrosis patients: Correlation with fat-free mass
32. Monitoring of 25-OH vitamin D levels in children with cystic fibrosis
33. Functional iron deficiency in adults with cystic fibrosis
34. Nutrition intervention for weight gain in cystic fibrosis: A meta analysis
35. Percutaneous endoscopic gastrostomy feeding improves nutritional status and stabilizes pulmonary function in patients with cystic fibrosis
36. Pulmonary function correlates in the prediction of long-term weight gain in cystic fibrosis patients with gastrostomy tube feedings
37. Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis