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Comprehensive Physiology
|
June 6, 2013
Gas exchange in disease: asthma, chronic obstructive pulmonary disease, cystic fibrosis, and interstitial lung disease
Iven H Young, Peter T P Bye
Paediatric Respiratory Reviews
|
April 11, 2007
Other mucoactive agents for cystic fibrosis
Peter T P Bye, Mark R Elkins
Current Opinion in Pulmonary Medicine
|
October 21, 2006
Inhaled hypertonic saline as a therapy for cystic fibrosis
Mark R Elkins, Peter T P Bye
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Granulomatous diseases in a patient with cystic fibrosis
Catherine J Dobbin, Carmel Moriarty, Peter T P Bye
Journal of Physiotherapy
|
February 21, 2012
Adults with cystic fibrosis prefer hypertonic saline before or during airway clearance techniques: a randomised crossover trial
Ruth L Dentice, Mark R Elkins, Peter T P Bye
Chronic Respiratory Disease
|
March 29, 2012
Arm exercise training in chronic obstructive pulmonary disease: a randomised controlled trial
Zoe J McKeough, Peter T P Bye, Jennifer A Alison
Pediatric Pulmonology
|
September 1, 2005
Effect of body position on maximal expiratory pressure and flow in adults with cystic fibrosis
Mark R Elkins, Jennifer A Alison, Peter T P Bye
Journal of Cardiopulmonary Rehabilitation
|
June 5, 2003
Arm exercise capacity and dyspnea ratings in subjects with chronic obstructive pulmonary disease
Zoe J McKeough, Jennifer A Alison, Peter T P Bye
The Australian Journal of Physiotherapy
|
May 31, 2003
Arm positioning alters lung volumes in subjects with COPD and healthy subjects
Zoe J McKeough, Jennifer A Alison, Peter T P Bye
Current Opinion in Pulmonary Medicine
|
September 2, 2011
The role of exercise in maintaining health in cystic fibrosis
Tiffany J Dwyer, Mark R Elkins, Peter T P Bye
Page
of 4
Search research articles
Search
Showing results (1-10 of 40) with videos related to
Sort By:
Page
of 4
Comprehensive Physiology
|
June 6, 2013
Gas exchange in disease: asthma, chronic obstructive pulmonary disease, cystic fibrosis, and interstitial lung disease
Iven H Young, Peter T P Bye
Paediatric Respiratory Reviews
|
April 11, 2007
Other mucoactive agents for cystic fibrosis
Peter T P Bye, Mark R Elkins
Current Opinion in Pulmonary Medicine
|
October 21, 2006
Inhaled hypertonic saline as a therapy for cystic fibrosis
Mark R Elkins, Peter T P Bye
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Granulomatous diseases in a patient with cystic fibrosis
Catherine J Dobbin, Carmel Moriarty, Peter T P Bye
Journal of Physiotherapy
|
February 21, 2012
Adults with cystic fibrosis prefer hypertonic saline before or during airway clearance techniques: a randomised crossover trial
Ruth L Dentice, Mark R Elkins, Peter T P Bye
Chronic Respiratory Disease
|
March 29, 2012
Arm exercise training in chronic obstructive pulmonary disease: a randomised controlled trial
Zoe J McKeough, Peter T P Bye, Jennifer A Alison
Pediatric Pulmonology
|
September 1, 2005
Effect of body position on maximal expiratory pressure and flow in adults with cystic fibrosis
Mark R Elkins, Jennifer A Alison, Peter T P Bye
Journal of Cardiopulmonary Rehabilitation
|
June 5, 2003
Arm exercise capacity and dyspnea ratings in subjects with chronic obstructive pulmonary disease
Zoe J McKeough, Jennifer A Alison, Peter T P Bye
The Australian Journal of Physiotherapy
|
May 31, 2003
Arm positioning alters lung volumes in subjects with COPD and healthy subjects
Zoe J McKeough, Jennifer A Alison, Peter T P Bye
Current Opinion in Pulmonary Medicine
|
September 2, 2011
The role of exercise in maintaining health in cystic fibrosis
Tiffany J Dwyer, Mark R Elkins, Peter T P Bye
Page
of 4