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Thorax
|
April 8, 1999
Retransplantation in a patient with cystic fibrosis
M McCloskey, A P Maxwell, V Hall, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
June 16, 2001
Total energy expenditure in stable patients with cystic fibrosis
M McCloskey, A O Redmond, S Pyper, et al.
Scandinavian Journal of Gastroenterology. Supplement
|
January 1, 1983
The diffuse endocrine system in cystic fibrosis
K 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 chromosomes
D 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 mutations
A 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 patients
H 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 fibrosis
G 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 fibrosis
R M Wright, J E Moore, A Shaw, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 18) with videos related to
Sort By:
Page
of 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 fibrosis
M McCloskey, A P Maxwell, V Hall, et al.
Clinical Nutrition (Edinburgh, Scotland)
|
June 16, 2001
Total energy expenditure in stable patients with cystic fibrosis
M McCloskey, A O Redmond, S Pyper, et al.
Scandinavian Journal of Gastroenterology. Supplement
|
January 1, 1983
The diffuse endocrine system in cystic fibrosis
K 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 chromosomes
D 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 mutations
A 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 patients
H 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 fibrosis
G 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 fibrosis
R M Wright, J E Moore, A Shaw, et al.
Page
of 2