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P G Noone

Showing results (11-20 of 22) with videos related to

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The Journal of Pediatrics|September 20, 2001
A modified technique for measurement of nasal transepithelial potential difference in infantsK W Southern, P G Noone, D G Bosworth, et al.
Chest|November 21, 1997
Airway deposition and clearance and systemic pharmacokinetics of amiloride following aerosolization with an ultrasonic nebulizer to normal airwaysP G Noone, J A Regnis, X Liu, et al.
The New England Journal of Medicine|September 3, 1998
Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitisJ A Cohn, K J Friedman, P G Noone, et al.
American Journal of Respiratory and Critical Care Medicine|June 25, 1998
Bronchial artery embolization for the treatment of hemoptysis in patients with cystic fibrosisG M Brinson, P G Noone, M A Mauro, et al.
American Journal of Respiratory Cell and Molecular Biology|November 20, 2001
Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesiaM Zariwala, P G Noone, A Sannuti, et al.
American Journal of Respiratory and Critical Care Medicine|July 3, 1999
Effect of aerosolized uridine-5'-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesiaP G Noone, W D Bennett, J A Regnis, et al.
Thorax|May 31, 2003
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutationsA Kispert, M Petry, H Olbrich, et al.
Human Gene Therapy|February 24, 1998
A double-blind, placebo controlled, dose ranging study to evaluate the safety and biological efficacy of the lipid-DNA complex GR213487B in the nasal epithelium of adult patients with cystic fibrosisM R Knowles, P G Noone, K Hohneker, et al.
American Journal of Medical Genetics|February 6, 1999
Discordant organ laterality in monozygotic twins with primary ciliary dyskinesiaP G Noone, D Bali, J L Carson, et al.
American Journal of Respiratory and Critical Care Medicine|November 9, 2000
Lung disease associated with the IVS8 5T allele of the CFTR geneP G Noone, C A Pue, Z Zhou, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
The Journal of Pediatrics|September 20, 2001
A modified technique for measurement of nasal transepithelial potential difference in infantsK W Southern, P G Noone, D G Bosworth, et al.
Chest|November 21, 1997
Airway deposition and clearance and systemic pharmacokinetics of amiloride following aerosolization with an ultrasonic nebulizer to normal airwaysP G Noone, J A Regnis, X Liu, et al.
The New England Journal of Medicine|September 3, 1998
Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitisJ A Cohn, K J Friedman, P G Noone, et al.
American Journal of Respiratory and Critical Care Medicine|June 25, 1998
Bronchial artery embolization for the treatment of hemoptysis in patients with cystic fibrosisG M Brinson, P G Noone, M A Mauro, et al.
American Journal of Respiratory Cell and Molecular Biology|November 20, 2001
Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesiaM Zariwala, P G Noone, A Sannuti, et al.
American Journal of Respiratory and Critical Care Medicine|July 3, 1999
Effect of aerosolized uridine-5'-triphosphate on airway clearance with cough in patients with primary ciliary dyskinesiaP G Noone, W D Bennett, J A Regnis, et al.
Thorax|May 31, 2003
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutationsA Kispert, M Petry, H Olbrich, et al.
Human Gene Therapy|February 24, 1998
A double-blind, placebo controlled, dose ranging study to evaluate the safety and biological efficacy of the lipid-DNA complex GR213487B in the nasal epithelium of adult patients with cystic fibrosisM R Knowles, P G Noone, K Hohneker, et al.
American Journal of Medical Genetics|February 6, 1999
Discordant organ laterality in monozygotic twins with primary ciliary dyskinesiaP G Noone, D Bali, J L Carson, et al.
American Journal of Respiratory and Critical Care Medicine|November 9, 2000
Lung disease associated with the IVS8 5T allele of the CFTR geneP G Noone, C A Pue, Z Zhou, et al.
Pageof 3