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Pediatric Pulmonology
|
July 18, 2017
Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers
Olivia Giddings, Charles R Esther
Pediatric Pulmonology
|
August 31, 2004
Pulmonary lymphangiectasia: diagnosis and clinical course
Charles R Esther, Pierre M Barker
Current Opinion in Pharmacology
|
June 1, 2022
Metabolomics of airways disease in cystic fibrosis
Joshua D Chandler, Charles R Esther
American Journal of Respiratory and Critical Care Medicine
|
August 28, 2019
Identifying Biomarkers in Pediatric Rare Lung Disease. chILD Grows Up
Timothy J Vece, Charles R Esther
Infection Control and Hospital Epidemiology
|
March 3, 2015
Detection of Mycobacterium abscessus from deep pharyngeal swabs in cystic fibrosis
Charles R Esther, Alan Kerr, Peter H Gilligan
Expert Review of Precision Medicine and Drug Development
|
August 3, 2016
Efficacy of lumacaftor-ivacaftor for the treatment of cystic fibrosis patients homozygous for the F508del-CFTR mutation
Deborah M Cholon, Charles R Esther, Martina Gentzsch
Pediatric Pulmonology
|
February 18, 2011
Impact of an evidence-based algorithm on quality of care in pediatric parapneumonic effusion and empyema
Kyrie L Shomaker, Tim Weiner, Charles R Esther
Sub-Cellular Biochemistry
|
May 12, 2011
Regulation of airway nucleotides in chronic lung diseases
Charles R Esther, Neil E Alexis, Maryse Picher
Journal of Breath Research
|
December 16, 2017
Transition and post-transition metals in exhaled breath condensate
Andrew J Ghio, Michael C Madden, Charles R Esther
The Lancet. Respiratory Medicine
|
October 12, 2024
Airway inflammation enhances the effectiveness of elexacaftor-tezacaftor-ivacaftor therapy for cystic fibrosis and CFTR<sup>N1303K</sup> mutation
Martina Gentzsch, Charles R Esther, Carla M P Ribeiro
Page
of 11
Search research articles
Search
Showing results (1-10 of 103) with videos related to
Sort By:
Page
of 11
Pediatric Pulmonology
|
July 18, 2017
Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers
Olivia Giddings, Charles R Esther
Pediatric Pulmonology
|
August 31, 2004
Pulmonary lymphangiectasia: diagnosis and clinical course
Charles R Esther, Pierre M Barker
Current Opinion in Pharmacology
|
June 1, 2022
Metabolomics of airways disease in cystic fibrosis
Joshua D Chandler, Charles R Esther
American Journal of Respiratory and Critical Care Medicine
|
August 28, 2019
Identifying Biomarkers in Pediatric Rare Lung Disease. chILD Grows Up
Timothy J Vece, Charles R Esther
Infection Control and Hospital Epidemiology
|
March 3, 2015
Detection of Mycobacterium abscessus from deep pharyngeal swabs in cystic fibrosis
Charles R Esther, Alan Kerr, Peter H Gilligan
Expert Review of Precision Medicine and Drug Development
|
August 3, 2016
Efficacy of lumacaftor-ivacaftor for the treatment of cystic fibrosis patients homozygous for the F508del-CFTR mutation
Deborah M Cholon, Charles R Esther, Martina Gentzsch
Pediatric Pulmonology
|
February 18, 2011
Impact of an evidence-based algorithm on quality of care in pediatric parapneumonic effusion and empyema
Kyrie L Shomaker, Tim Weiner, Charles R Esther
Sub-Cellular Biochemistry
|
May 12, 2011
Regulation of airway nucleotides in chronic lung diseases
Charles R Esther, Neil E Alexis, Maryse Picher
Journal of Breath Research
|
December 16, 2017
Transition and post-transition metals in exhaled breath condensate
Andrew J Ghio, Michael C Madden, Charles R Esther
The Lancet. Respiratory Medicine
|
October 12, 2024
Airway inflammation enhances the effectiveness of elexacaftor-tezacaftor-ivacaftor therapy for cystic fibrosis and CFTR<sup>N1303K</sup> mutation
Martina Gentzsch, Charles R Esther, Carla M P Ribeiro
Page
of 11