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A O Redmond

Showing results (11-20 of 18) with videos related to

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Thorax|April 8, 1999
Retransplantation in a patient with cystic fibrosisM McCloskey, A P Maxwell, V Hall, et al.
Clinical Nutrition (Edinburgh, Scotland)|June 16, 2001
Total energy expenditure in stable patients with cystic fibrosisM McCloskey, A O Redmond, S Pyper, et al.
Scandinavian Journal of Gastroenterology. Supplement|January 1, 1983
The diffuse endocrine system in cystic fibrosisK D Buchanan, J I Kerr, C F Johnston, et al.
Human Mutation|January 1, 1996
Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomesD J Hughes, A J Hill, M Macek, et al.
Clinical Science (London, England : 1979)|January 1, 1992
Increased energy expenditure in cystic fibrosis is associated with specific mutationsA O'Rawe, I McIntosh, J A Dodge, et al.
The Journal of Antimicrobial Chemotherapy|November 1, 1989
Clinical and pharmacokinetic aspects of ciprofloxacin in the treatment of acute exacerbations of pseudomonas infection in cystic fibrosis patientsH J Steen, E M Scott, M I Stevenson, et al.
Alimentary Pharmacology & Therapeutics|October 1, 1992
Comparison between a standard pancreatic supplement and a high enzyme preparation in cystic fibrosisG Morrison, J M Morrison, A O Redmond, et al.
Journal of Clinical Pathology|September 29, 2001
Improved cultural detection of Burkholderia cepacia from sputum in patients with cystic fibrosisR M Wright, J E Moore, A Shaw, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Thorax|April 8, 1999
Retransplantation in a patient with cystic fibrosisM McCloskey, A P Maxwell, V Hall, et al.
Clinical Nutrition (Edinburgh, Scotland)|June 16, 2001
Total energy expenditure in stable patients with cystic fibrosisM McCloskey, A O Redmond, S Pyper, et al.
Scandinavian Journal of Gastroenterology. Supplement|January 1, 1983
The diffuse endocrine system in cystic fibrosisK D Buchanan, J I Kerr, C F Johnston, et al.
Human Mutation|January 1, 1996
Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomesD J Hughes, A J Hill, M Macek, et al.
Clinical Science (London, England : 1979)|January 1, 1992
Increased energy expenditure in cystic fibrosis is associated with specific mutationsA O'Rawe, I McIntosh, J A Dodge, et al.
The Journal of Antimicrobial Chemotherapy|November 1, 1989
Clinical and pharmacokinetic aspects of ciprofloxacin in the treatment of acute exacerbations of pseudomonas infection in cystic fibrosis patientsH J Steen, E M Scott, M I Stevenson, et al.
Alimentary Pharmacology & Therapeutics|October 1, 1992
Comparison between a standard pancreatic supplement and a high enzyme preparation in cystic fibrosisG Morrison, J M Morrison, A O Redmond, et al.
Journal of Clinical Pathology|September 29, 2001
Improved cultural detection of Burkholderia cepacia from sputum in patients with cystic fibrosisR M Wright, J E Moore, A Shaw, et al.
Pageof 2