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G Mastella

Showing results (21-30 of 73) with videos related to

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Enzyme|January 1, 1989
Prenatal diagnosis of cystic fibrosis. Analytical evaluation of microvillar enzyme determinations in amniotic fluidM C Dechecchi, E Girella, G Borgo, et al.
Helvetica Paediatrica Acta|June 1, 1989
Pulmonary hemosiderosis in a child with cystic fibrosisE A Valletta, M Cipolli, G Cazzola, et al.
Pediatric Pulmonology|June 1, 1995
Bronchial artery embolization in the management of hemoptysis in cystic fibrosisM Cipolli, S Perini, E A Valletta, et al.
European Journal of Pediatrics|April 1, 1996
Deficiency of vitamins E and A in cystic fibrosis is independent of pancreatic function and current enzyme and vitamin supplementationL Lancellotti, C D'Orazio, G Mastella, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 1997
Failure to thrive: the earliest feature of cystic fibrosis in infants diagnosed by neonatal screeningL Giglio, M Candusso, C D'Orazio, et al.
The European Respiratory Journal|May 1, 1997
Nasal potential difference in cystic fibrosis patients presenting borderline sweat testA Delmarco, U Pradal, G Cabrini, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
A more objective approach to the evaluation of antimicrobial therapy in cystic fibrosisE A Valletta, A Rigo, L Bonazzi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1992
Modification of some markers of inflammation during treatment for acute respiratory exacerbation in cystic fibrosisE A Valletta, A Rigo, L Bonazzi, et al.
Genetic Testing|January 15, 2002
A pilot survey of cystic fibrosis clinical manifestations in CFTR mutation heterozygotesC Castellani, C Quinzii, S Altieri, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 8, 2000
Reliability of sweat-testing by the Macroduct collection method combined with conductivity analysis in comparison with the classic Gibson and Cooke techniqueG Mastella, G Di Cesare, A Borruso, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Enzyme|January 1, 1989
Prenatal diagnosis of cystic fibrosis. Analytical evaluation of microvillar enzyme determinations in amniotic fluidM C Dechecchi, E Girella, G Borgo, et al.
Helvetica Paediatrica Acta|June 1, 1989
Pulmonary hemosiderosis in a child with cystic fibrosisE A Valletta, M Cipolli, G Cazzola, et al.
Pediatric Pulmonology|June 1, 1995
Bronchial artery embolization in the management of hemoptysis in cystic fibrosisM Cipolli, S Perini, E A Valletta, et al.
European Journal of Pediatrics|April 1, 1996
Deficiency of vitamins E and A in cystic fibrosis is independent of pancreatic function and current enzyme and vitamin supplementationL Lancellotti, C D'Orazio, G Mastella, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 24, 1997
Failure to thrive: the earliest feature of cystic fibrosis in infants diagnosed by neonatal screeningL Giglio, M Candusso, C D'Orazio, et al.
The European Respiratory Journal|May 1, 1997
Nasal potential difference in cystic fibrosis patients presenting borderline sweat testA Delmarco, U Pradal, G Cabrini, et al.
Acta Universitatis Carolinae. Medica|January 1, 1990
A more objective approach to the evaluation of antimicrobial therapy in cystic fibrosisE A Valletta, A Rigo, L Bonazzi, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 1, 1992
Modification of some markers of inflammation during treatment for acute respiratory exacerbation in cystic fibrosisE A Valletta, A Rigo, L Bonazzi, et al.
Genetic Testing|January 15, 2002
A pilot survey of cystic fibrosis clinical manifestations in CFTR mutation heterozygotesC Castellani, C Quinzii, S Altieri, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 8, 2000
Reliability of sweat-testing by the Macroduct collection method combined with conductivity analysis in comparison with the classic Gibson and Cooke techniqueG Mastella, G Di Cesare, A Borruso, et al.
Pageof 8