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P Clancy

Showing results (61-70 of 226) with videos related to

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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 16, 2015
Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftorChristopher M Siracusa, Jamie Ryan, Lisa Burns, et al.
Genomics|December 15, 1996
Localization of the L-glutamine synthetase gene to chromosome 1q23K P Clancy, R Berger, M Cox, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 11, 2014
Daily serum creatinine monitoring promotes earlier detection of acute kidney injury in children and adolescents with cystic fibrosisKevin J Downes, Marepalli B Rao, Laurie Kahill, et al.
International Journal of Medical Sciences|January 23, 2009
Matrix metalloproteinase activity in pediatric acute lung injuryMichele Y F Kong, Amit Gaggar, Yao Li, et al.
American Journal of Respiratory and Critical Care Medicine|April 16, 2017
Phenotypes of Rapid Cystic Fibrosis Lung Disease Progression during Adolescence and Young AdulthoodRhonda D Szczesniak, Dan Li, Weiji Su, et al.
Annals of Epidemiology|October 10, 2013
A semiparametric approach to estimate rapid lung function decline in cystic fibrosisRhonda D Szczesniak, Gary L McPhail, Leo L Duan, et al.
International Journal of Molecular Sciences|January 21, 2023
Phenotypic Alteration of an Established Human Airway Cell Line by Media SelectionGalit Livnat, Jessica D Meeker, Alicia J Ostmann, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 2, 2016
Hyperpolarized <sup>129</sup>Xe for investigation of mild cystic fibrosis lung disease in pediatric patientsRobert P Thomen, Laura L Walkup, David J Roach, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 10, 2020
Changes in LCI in F508del/F508del patients treated with lumacaftor/ivacaftor: Results from the prospect studyMichelle Shaw, Umer Khan, John P Clancy, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|March 27, 2007
Matrix metalloprotease-9 dysregulation in lower airway secretions of cystic fibrosis patientsAmit Gaggar, Yao Li, Nathaniel Weathington, et al.
Pageof 23

Showing results (61-70 of 226) with videos related to

Sort By:
Pageof 23
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 16, 2015
Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftorChristopher M Siracusa, Jamie Ryan, Lisa Burns, et al.
Genomics|December 15, 1996
Localization of the L-glutamine synthetase gene to chromosome 1q23K P Clancy, R Berger, M Cox, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 11, 2014
Daily serum creatinine monitoring promotes earlier detection of acute kidney injury in children and adolescents with cystic fibrosisKevin J Downes, Marepalli B Rao, Laurie Kahill, et al.
International Journal of Medical Sciences|January 23, 2009
Matrix metalloproteinase activity in pediatric acute lung injuryMichele Y F Kong, Amit Gaggar, Yao Li, et al.
American Journal of Respiratory and Critical Care Medicine|April 16, 2017
Phenotypes of Rapid Cystic Fibrosis Lung Disease Progression during Adolescence and Young AdulthoodRhonda D Szczesniak, Dan Li, Weiji Su, et al.
Annals of Epidemiology|October 10, 2013
A semiparametric approach to estimate rapid lung function decline in cystic fibrosisRhonda D Szczesniak, Gary L McPhail, Leo L Duan, et al.
International Journal of Molecular Sciences|January 21, 2023
Phenotypic Alteration of an Established Human Airway Cell Line by Media SelectionGalit Livnat, Jessica D Meeker, Alicia J Ostmann, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 2, 2016
Hyperpolarized <sup>129</sup>Xe for investigation of mild cystic fibrosis lung disease in pediatric patientsRobert P Thomen, Laura L Walkup, David J Roach, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 10, 2020
Changes in LCI in F508del/F508del patients treated with lumacaftor/ivacaftor: Results from the prospect studyMichelle Shaw, Umer Khan, John P Clancy, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|March 27, 2007
Matrix metalloprotease-9 dysregulation in lower airway secretions of cystic fibrosis patientsAmit Gaggar, Yao Li, Nathaniel Weathington, et al.
Pageof 23