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Journal of Medical Genetics
|
August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease
P Gasparini, G Borgo, G Mastella, et al.
European Journal of Pediatrics
|
December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort study
G Borgo, P Gasparini, A Bonizzato, et al.
Journal of Medical Genetics
|
November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosis
G Borgo, G Mastella, P Gasparini, et al.
European Journal of Epidemiology
|
April 1, 1996
Field inversion gel electrophoresis on Pseudomonas cepacia strains isolated from cystic fibrosis patients
G Amalfitano, E Tonolli, F Favari, et al.
The Journal of Hospital Infection
|
July 13, 2006
Isolation measures for prevention of infection with respiratory pathogens in cystic fibrosis: a systematic review
F Festini, R Buzzetti, C Bassi, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 1, 1994
Determinants of maximal transdiaphragmatic pressure in adults with cystic fibrosis
U Pradal, G Polese, C Braggion, et al.
Biology of the Cell
|
January 1, 1988
Cilia-lacking respiratory cells in ciliary aplasia
M M de Santi, C Gardi, G Barlocco, et al.
Community Genetics
|
June 8, 2004
Carrier testing program in a high-risk cystic fibrosis population from northeastern Italy. Active recruitment of relatives via probands' parents
G Borgo, C Castellani, A Bonizzato, et al.
Pediatric Pulmonology
|
January 1, 1988
The saccharin method for testing mucociliary function in patients suspected of having primary ciliary dyskinesia
M Canciani, E G Barlocco, G Mastella, et al.
Journal of Clinical and Hospital Pharmacy
|
December 1, 1984
Serum and sputum concentrations of azlocillin, cefoperazone and ceftazidime in patients with cystic fibrosis
N Martini, M Agostini, G Barlocco, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 73) with videos related to
Sort By:
Page
of 8
Journal of Medical Genetics
|
August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung disease
P Gasparini, G Borgo, G Mastella, et al.
European Journal of Pediatrics
|
December 1, 1993
Cystic fibrosis: the delta F508 mutation does not lead to an exceptionally severe phenotype. A cohort study
G Borgo, P Gasparini, A Bonizzato, et al.
Journal of Medical Genetics
|
November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosis
G Borgo, G Mastella, P Gasparini, et al.
European Journal of Epidemiology
|
April 1, 1996
Field inversion gel electrophoresis on Pseudomonas cepacia strains isolated from cystic fibrosis patients
G Amalfitano, E Tonolli, F Favari, et al.
The Journal of Hospital Infection
|
July 13, 2006
Isolation measures for prevention of infection with respiratory pathogens in cystic fibrosis: a systematic review
F Festini, R Buzzetti, C Bassi, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 1, 1994
Determinants of maximal transdiaphragmatic pressure in adults with cystic fibrosis
U Pradal, G Polese, C Braggion, et al.
Biology of the Cell
|
January 1, 1988
Cilia-lacking respiratory cells in ciliary aplasia
M M de Santi, C Gardi, G Barlocco, et al.
Community Genetics
|
June 8, 2004
Carrier testing program in a high-risk cystic fibrosis population from northeastern Italy. Active recruitment of relatives via probands' parents
G Borgo, C Castellani, A Bonizzato, et al.
Pediatric Pulmonology
|
January 1, 1988
The saccharin method for testing mucociliary function in patients suspected of having primary ciliary dyskinesia
M Canciani, E G Barlocco, G Mastella, et al.
Journal of Clinical and Hospital Pharmacy
|
December 1, 1984
Serum and sputum concentrations of azlocillin, cefoperazone and ceftazidime in patients with cystic fibrosis
N Martini, M Agostini, G Barlocco, et al.
Page
of 8