Improvements of lung function in cystic fibrosis

Pediatric Pulmonology

Volumn 33, Issue 4, 2002, Pages 263-268

  Tauber, Erich ^a   Eichler, Irmgard ^a   Gartner, Christian ^a   Halmerbauer, Gerhard ^a   Götz, Manfred ^b   Rath, Regina ^a   Wojnarowski, Claudia ^b   Frischer, Thomas ^a  

^a ST ANNA CHILDREN S HOSPITAL   (Austria)

^b WILHELMINEN HOSPITAL   (Austria)

Author keywords

Childhood; Cystic fibrosis; Infant; Lung function; Natural history

Indexed keywords

ARTICLE; BODY HEIGHT; BODY WEIGHT; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; GENDER; HUMAN; INFANT; LUNG FUNCTION; MAJOR CLINICAL STUDY; MALE; MODEL; PATIENT CARE; PREDICTION; PRESCHOOL CHILD; PRIORITY JOURNAL; REGRESSION ANALYSIS; SURVIVAL;

CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; DISEASE PROGRESSION; FEMALE; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; HUMANS; INFANT; LINEAR MODELS; MALE; MULTIVARIATE ANALYSIS; OUTCOME ASSESSMENT (HEALTH CARE); PULMONARY VENTILATION; RESPIRATORY FUNCTION TESTS; RETROSPECTIVE STUDIES; WEIGHT GAIN;

EID: 0036209027     PISSN: 87556863     EISSN: None     Source Type: Journal    
DOI: 10.1002/ppul.10076     Document Type: Article

References (18)

1. Basic therapies in cystic fibrosis. Does standard therapy work?
2. Cystic fibrosis of the pancreas and its relation to celiac disease: A clinical and pathological study
3. Cystic fibrosis current survival and population estimate to the year 2000
4. Clinical outcome in relation to care in centres specialising in cystic fibrosis: Cross sectional study
5. Assessment of the respiratory status of infants and toddlers with cystic fibrosis
6. Airway resistance and lung volume in new-born infants
7. Plethysmographic assessment of functional residual capacity and airway resistance
8. Standardization of spirometry - 1987 Update
9. Lung function in white children aged 4 to 19 years: I. Spirometry
10. Lung function in white children aged 4 to 19 years: II. Single breath analysis and plethysmography
11. Lung function in infants with cystic fibrosis
12. Pulmonary function in infants with cystic fibrosis
13. Lung function from infancy to school age in cystic fibrosis
14. Flow-volume relationship at low lung volumes in healthy term newborn infants
15. Cystic fibrosis
16. Use of antibiotics in cystic fibrosis. The Danish approach
17. Long-term azithromycin may improve lung function in children with cystic fibrosis
18. Finding evidence to support airway clearance techniques in cystic fibrosis