Time constant of inspiratory muscle relaxation in cystic fibrosis-Reference-Cited by-同舟云学术

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Time constant of inspiratory muscle relaxation in cystic fibrosis

Published:2015-02-02 Issue:4 Volume:77 Page:541-545
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Dassios Theodore,Kaditis Athanasios,Katelari Anna,Chrousos George,Doudounakis Stavros,Dimitriou Gabriel

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Link

http://www.nature.com/articles/pr20152.pdf

Reference30 articles.

1. Hart N, Polkey MI, Clément A, et al. Changes in pulmonary mechanics with increasing disease severity in children and young adults with cystic fibrosis. Am J Respir Crit Care Med 2002;166:61–6.

2. Hayot M, Guillaumont S, Ramonatxo M, Voisin M, Préfaut C . Determinants of the tension-time index of inspiratory muscles in children with cystic fibrosis. Pediatr Pulmonol 1997;23:336–43.

3. Hahn A, Ankermann T, Claass A, Mann M, Lindemann H, Neubauer BA . Non-invasive tension time index in relation to severity of disease in children with cystic fibrosis. Pediatr Pulmonol 2008;43:973–81.

4. Divangahi M, Matecki S, Dudley RW, et al. Preferential diaphragmatic weakness during sustained Pseudomonas aeruginosa lung infection. Am J Respir Crit Care Med 2004;169:679–86.

5. Dassios TG, Katelari A, Doudounakis S, Dimitriou G . Chronic Pseudomonas aeruginosa infection and respiratory muscle impairment in cystic fibrosis. Respir Care 2014;59:363–70.

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