Respiratory muscle function in cystic fibrosis.

Author:

Mier A,Redington A,Brophy C,Hodson M,Green M

Publisher

BMJ

Subject

Pulmonary and Respiratory Medicine

Reference10 articles.

1. Effect of body weight and muscularity on human diaphragm muscle mass, thickness and area;Arora, N.; Rochester, D.;J Appl Physiol,1982

2. Respiratory muscle strength and maximum voluntary ventilation in undernourished patients;Arora, N.; Rochester, D.;Am Rev Respir Dis,1982

3. Maximal inspiratory and expiratory pressures are reduced in hyperinflated, malnourished young adult male patients with cystic fibrosis;Szeinberg, A.; England, S.; Mindorff, C.; Fraser, I.; Levison, H.;Am Rev Respir Dis,1985

4. Increased ventilatory muscle strength and endurance in childhood with asthma and cystic;Nickerson, B.G.; Richards, W.; Wang, C.; Keens, T.G.

5. The effects of inspiratory muscle training in patients with cystic fibrosis;Asher, M.I.; Pardy, R.L.; Coates, A.L.; Thomas, E.; Macklem, P.;Am Rev Respir Dis,1982

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