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G Mastella

Showing results (41-50 of 73) with videos related to

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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 diseaseP 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 studyG Borgo, P Gasparini, A Bonizzato, et al.
Journal of Medical Genetics|November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosisG 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 patientsG 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 reviewF 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 fibrosisU Pradal, G Polese, C Braggion, et al.
Biology of the Cell|January 1, 1988
Cilia-lacking respiratory cells in ciliary aplasiaM 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' parentsG 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 dyskinesiaM 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 fibrosisN Martini, M Agostini, G Barlocco, et al.
Pageof 8

Showing results (41-50 of 73) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|August 1, 1992
Nine cystic fibrosis patients homozygous for the CFTR nonsense mutation R1162X have mild or moderate lung diseaseP 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 studyG Borgo, P Gasparini, A Bonizzato, et al.
Journal of Medical Genetics|November 1, 1990
Pancreatic function and gene deletion F508 in cystic fibrosisG 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 patientsG 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 reviewF 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 fibrosisU Pradal, G Polese, C Braggion, et al.
Biology of the Cell|January 1, 1988
Cilia-lacking respiratory cells in ciliary aplasiaM 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' parentsG 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 dyskinesiaM 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 fibrosisN Martini, M Agostini, G Barlocco, et al.
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