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British Journal of Clinical Pharmacology
|
December 1, 1994
Inhibition of caffeine metabolism by ciprofloxacin in children with cystic fibrosis as measured by the caffeine breath test
A C Parker, T Preston, D Heaf, et al.
Lancet (London, England)
|
August 14, 1993
Transmission of Pseudomonas cepacia by social contact in cystic fibrosis
A Smyth, D Heaf, J Corkill, et al.
Archives of Disease in Childhood
|
February 1, 1994
Diagnosis of interstitial lung disease by a percutaneous lung biopsy sample
R L Smyth, H Carty, H Thomas, et al.
Clinical Radiology
|
July 1, 1994
Strictures of the colon in cystic fibrosis
S J King, D Van Velzen, R L Smyth, et al.
Archives of Disease in Childhood
|
August 1, 1987
Glycosylated haemoglobin and glucose intolerance in cystic fibrosis
P R Stutchfield, S O'Halloran, J D Teale, et al.
Pediatric Research
|
March 1, 1994
Effect of pH and CO2 on in vitro susceptibility of Pseudomonas cepacia to beta-lactams
J E Corkill, J Deveney, J Pratt, et al.
Archives of Disease in Childhood
|
December 1, 1996
Clinical significance of cough and wheeze in the diagnosis of asthma
Y J Kelly, B J Brabin, P J Milligan, et al.
Archives of Disease in Childhood
|
October 1, 1988
HLA type, islet cell antibodies, and glucose intolerance in cystic fibrosis
P R Stutchfield, S M O'Halloran, C S Smith, et al.
Journal of Medical Microbiology
|
August 1, 1994
Application of pyrolysis mass spectroscopy and SDS-PAGE in the study of the epidemiology of Pseudomonas cepacia in cystic fibrosis
J E Corkill, P R Sisson, A Smyth, et al.
Lancet (London, England)
|
February 4, 1984
Spontaneous remission of multi-system histiocytosis X
V Broadbent, J Pritchard, E G Davies, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
British Journal of Clinical Pharmacology
|
December 1, 1994
Inhibition of caffeine metabolism by ciprofloxacin in children with cystic fibrosis as measured by the caffeine breath test
A C Parker, T Preston, D Heaf, et al.
Lancet (London, England)
|
August 14, 1993
Transmission of Pseudomonas cepacia by social contact in cystic fibrosis
A Smyth, D Heaf, J Corkill, et al.
Archives of Disease in Childhood
|
February 1, 1994
Diagnosis of interstitial lung disease by a percutaneous lung biopsy sample
R L Smyth, H Carty, H Thomas, et al.
Clinical Radiology
|
July 1, 1994
Strictures of the colon in cystic fibrosis
S J King, D Van Velzen, R L Smyth, et al.
Archives of Disease in Childhood
|
August 1, 1987
Glycosylated haemoglobin and glucose intolerance in cystic fibrosis
P R Stutchfield, S O'Halloran, J D Teale, et al.
Pediatric Research
|
March 1, 1994
Effect of pH and CO2 on in vitro susceptibility of Pseudomonas cepacia to beta-lactams
J E Corkill, J Deveney, J Pratt, et al.
Archives of Disease in Childhood
|
December 1, 1996
Clinical significance of cough and wheeze in the diagnosis of asthma
Y J Kelly, B J Brabin, P J Milligan, et al.
Archives of Disease in Childhood
|
October 1, 1988
HLA type, islet cell antibodies, and glucose intolerance in cystic fibrosis
P R Stutchfield, S M O'Halloran, C S Smith, et al.
Journal of Medical Microbiology
|
August 1, 1994
Application of pyrolysis mass spectroscopy and SDS-PAGE in the study of the epidemiology of Pseudomonas cepacia in cystic fibrosis
J E Corkill, P R Sisson, A Smyth, et al.
Lancet (London, England)
|
February 4, 1984
Spontaneous remission of multi-system histiocytosis X
V Broadbent, J Pritchard, E G Davies, et al.
Page
of 3