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Thorax
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October 1, 1980
Unilateral hyperlucent lung: the case for investigation
S A McKenzie, D J Allison, M P Singh, et al.
Acta Paediatrica Scandinavica
|
May 1, 1980
The role of nutritional status, airway obstruction, hypoxia, and abnormalities in serum lipid composition in limiting exercise tolerance in children with cystic fibrosis
A L Coates, P Boyce, D Muller, et al.
The European Respiratory Journal
|
May 4, 2001
Plethysmographic measurements of lung volume and airway resistance. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/ American Thoracic Society
J Stocks, S Godfrey, C Beardsmore, et al.
The Journal of Pharmacy and Pharmacology
|
December 1, 1974
Proceedings: Disposition of disodium cromoglycate administered in three particle sizes
S H Curry, A J Taylor, S Evans, et al.
British Journal of Diseases of the Chest
|
January 1, 1971
Ear lobe blood samples for blood gas analysis at rest and during exercise
S Godfrey, E R Wozniak, R J Courtenay Evans, et al.
American Journal of Surgery
|
October 1, 1992
Nissen fundoplication in the treatment of children with familial dysautonomia
R Udassin, D Seror, I Vinograd, et al.
Respiration; International Review of Thoracic Diseases
|
January 1, 1986
Airway resistance measurements throughout the respiratory cycle in infants
C S Beardsmore, S Godfrey, N Shani, et al.
Pediatric Pulmonology
|
May 1, 1987
Is there a place for rigid bronchoscopy in the management of pediatric lung disease?
S Godfrey, C Springer, C Maayan, et al.
The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society
|
January 1, 1989
Surgical management of unresectable retroperitoneal leiomyosarcomas
T C Engelhardt, R S Godfrey, A L Levin, et al.
Archives of Disease in Childhood
|
February 1, 1981
Relationship between the chest radiograph, regional lung function studies, exercise tolerance, and clinical condition in cystic fibrosis
A L Coates, P Boyce, D G Shaw, et al.
Page
of 35
Search research articles
Search
Showing results (241-250 of 347) with videos related to
Sort By:
Page
of 35
Thorax
|
October 1, 1980
Unilateral hyperlucent lung: the case for investigation
S A McKenzie, D J Allison, M P Singh, et al.
Acta Paediatrica Scandinavica
|
May 1, 1980
The role of nutritional status, airway obstruction, hypoxia, and abnormalities in serum lipid composition in limiting exercise tolerance in children with cystic fibrosis
A L Coates, P Boyce, D Muller, et al.
The European Respiratory Journal
|
May 4, 2001
Plethysmographic measurements of lung volume and airway resistance. ERS/ATS Task Force on Standards for Infant Respiratory Function Testing. European Respiratory Society/ American Thoracic Society
J Stocks, S Godfrey, C Beardsmore, et al.
The Journal of Pharmacy and Pharmacology
|
December 1, 1974
Proceedings: Disposition of disodium cromoglycate administered in three particle sizes
S H Curry, A J Taylor, S Evans, et al.
British Journal of Diseases of the Chest
|
January 1, 1971
Ear lobe blood samples for blood gas analysis at rest and during exercise
S Godfrey, E R Wozniak, R J Courtenay Evans, et al.
American Journal of Surgery
|
October 1, 1992
Nissen fundoplication in the treatment of children with familial dysautonomia
R Udassin, D Seror, I Vinograd, et al.
Respiration; International Review of Thoracic Diseases
|
January 1, 1986
Airway resistance measurements throughout the respiratory cycle in infants
C S Beardsmore, S Godfrey, N Shani, et al.
Pediatric Pulmonology
|
May 1, 1987
Is there a place for rigid bronchoscopy in the management of pediatric lung disease?
S Godfrey, C Springer, C Maayan, et al.
The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society
|
January 1, 1989
Surgical management of unresectable retroperitoneal leiomyosarcomas
T C Engelhardt, R S Godfrey, A L Levin, et al.
Archives of Disease in Childhood
|
February 1, 1981
Relationship between the chest radiograph, regional lung function studies, exercise tolerance, and clinical condition in cystic fibrosis
A L Coates, P Boyce, D G Shaw, et al.
Page
of 35