Effect of systemic inflammation on inspiratory and limb muscle strength and bulk in cystic fibrosis.
par Dufresne, Valérie
;Knoop, Christiane
;Van Muylem, Alain
;Malfroot, Anne;Lamotte, Michel
;Opdekamp, Christian;Deboeck, Gaël
;Cassart, Marie
;Stallenberg, Bernard
;Casimir, Georges
;Duchateau, Jean
;Estenne, Marc 
Référence American journal of respiratory and critical care medicine, 180, 2, page (153-158)
Publication Publié, 2009-07










Référence American journal of respiratory and critical care medicine, 180, 2, page (153-158)
Publication Publié, 2009-07
Article révisé par les pairs
Résumé : | Diaphragm thickness is increased in cystic fibrosis (CF), but it shows a marked variability between patients. The variable response of the diaphragm to loading may reflect the combined and opposite effects of training by the respiratory disease and systemic inflammation. |