Works matching IS 87556863 AND DT 2000 AND VI 30 AND IP 1
Results: 11
Input respiratory impedance measured by head generator in preschool children.
- Published in:
- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 47, doi. 10.1002/1099-0496(200007)30:1<47::AID-PPUL8>3.0.CO;2-W
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- Article
Risk factors for emergence of Stenotrophomonas maltophilia in cystic fibrosis.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 10, doi. 10.1002/1099-0496(200007)30:1<10::AID-PPUL3>3.0.CO;2-Q
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Ozone: A trigger for hospital pediatric asthma emergency room visits.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 41, doi. 10.1002/1099-0496(200007)30:1<41::AID-PPUL7>3.0.CO;2-4
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Overall and peripheral inhomogeneity of ventilation in patients with stable cystic fibrosis.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 3, doi. 10.1002/1099-0496(200007)30:1<3::AID-PPUL2>3.0.CO;2-L
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Effects of birthweight and oxygen supplementation on lung function in late childhood in children of very low birth weight.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 32, doi. 10.1002/1099-0496(200007)30:1<32::AID-PPUL6>3.0.CO;2-9
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Selected abstracts.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 73, doi. 10.1002/1099-0496(200007)30:1<73::AID-PPUL11>3.0.CO;2-3
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- Article
Classical respiratory physiology-Gone the way of the dinosaurs? Do we need a Jurassic Park?
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 1, doi. 10.1002/1099-0496(200007)30:1<1::AID-PPUL1>3.0.CO;2-Q
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French multicenter randomized double-blind placebo-controlled trial on nebulized amiloride in cystic fibrosis patients.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 25, doi. 10.1002/1099-0496(200007)30:1<25::AID-PPUL5>3.0.CO;2-C
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Fifteen-count breathlessness score: An objective measure for children.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 56, doi. 10.1002/1099-0496(200007)30:1<56::AID-PPUL9>3.0.CO;2-R
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Is primary prevention of asthma possible?
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 63, doi. 10.1002/1099-0496(200007)30:1<63::AID-PPUL10>3.0.CO;2-7
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- Article
Effect of a short course of rhDNase on cough and mucociliary clearance in patients with cystic fibrosis.
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- Pediatric Pulmonology, 2000, v. 30, n. 1, p. 16, doi. 10.1002/1099-0496(200007)30:1<16::AID-PPUL4>3.0.CO;2-H
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