1. Determinants of dyspnea and alveolar hypoventilation during exercise in cystic fibrosis: Impact of inspiratory muscle endurance 
Sylvie Leroy, Thierry Perez, Rémy Neviere, Bernard Aguilaniu, Benoît Wallaert 
Journal of Cystic Fibrosis 
Volume 10, Issue 3, Pages (May 2011)
DOI: /j.jcf
Copyright © 2010 European Cystic Fibrosis Society. Terms and Conditions

2. Fig. 1
Borg dyspnea at the end of the incremental exercise testing on a cycloergometer as a function of the inspiratory muscle endurance (IME) expressed as a percentage of maximal inspiratory pressure (Plim2/PImax%) (r=−0.72). Triangles represent patients from Group LwD and squares represent patients from Group SvD.
Journal of Cystic Fibrosis  , DOI: ( /j.jcf )
Copyright © 2010 European Cystic Fibrosis Society. Terms and Conditions

3. Fig. 2
PaCO2 at rest and at peak exercise are represented for both groups. Group A is represented by white rectangles. Group B is represented by grey rectangles.
Journal of Cystic Fibrosis  , DOI: ( /j.jcf )
Copyright © 2010 European Cystic Fibrosis Society. Terms and Conditions