Pediatric interstitial lung disease revisitedEditor's note: This is the third article in the series on Orphan Lung Disease.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 369, doi. 10.1002/ppul.20114
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Works matching IS 87556863 AND DT 2004 AND VI 38 AND IP 5
Results: 7
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Tracheal gas insufflation‐augmented continuous positive airway pressure in a spontaneously breathing model of neonatal respiratory distressSubmitted to the 2004 Annual Meeting of the Pediatric Academic Societies.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 386, doi. 10.1002/ppul.20094
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3
Children with smoking parents have a higher airway resistance measured by the interruption technique.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 419, doi. 10.1002/ppul.20093
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- Article
4
Quantitative air‐trapping analysis in children with mild cystic fibrosis lung disease.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 396, doi. 10.1002/ppul.20091
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5
Psychological and educational factors: Better predictors of work status than FEV1 in adults with cystic fibrosis.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 413, doi. 10.1002/ppul.20090
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- Article
6
Dornase alpha and exhaled NO in cystic fibrosisThis paper was presented in part at the European Respiratory Society Annual Congress 2001, Berlin, Germany.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 379, doi. 10.1002/ppul.20088
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- Article
7
Effect of deep inspiration on airway caliber in children with asthma.
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- Pediatric Pulmonology, 2004, v. 38, n. 5, p. 406, doi. 10.1002/ppul.20038
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- Article