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Pediatric Pulmonology
|
September 30, 2017
Powerful tools for genetic modification: Advances in gene editing
Erica A Roesch, Mitchell L Drumm
Expert Review of Respiratory Medicine
|
March 23, 2022
The use of tobramycin for Pseudomonas aeruginosa: a review
Stanley B Fiel, Erica A Roesch
Pediatric Pulmonology
|
July 13, 2018
Inflammation in cystic fibrosis: An update
Erica A Roesch, David P Nichols, James F Chmiel
Current Opinion in Pulmonary Medicine
|
August 23, 2023
Chronic daily respiratory care needs in people with cystic fibrosis treated with highly effective cystic fibrosis transmembrane conductance regulator modulators
Katherine E Wajda, Erica A Roesch, Alex H Gifford
Expert Review of Respiratory Medicine
|
August 23, 2024
The continuing need for dornase alfa for extracellular airway DNA hydrolysis in the era of CFTR modulators
Erica A Roesch, Abdelkader Rahmaoui, Robert A Lazarus, et al.
Frontiers in Pediatrics
|
November 7, 2024
Case Report: A delicate equilibrium of exocrine pancreatic recovery and hepatotoxicity with elexacaftor/tezacaftor/ivacaftor therapy in a pediatric patient with cystic fibrosis
Michael P Coughlin, Senthilkumar Sankararaman, Erica A Roesch, et al.
Pharmaceuticals (Basel, Switzerland)
|
June 1, 2023
Human Mesenchymal Stem Cell (hMSC) Donor Potency Selection for the "First in Cystic Fibrosis" Phase I Clinical Trial (CEASE-CF)
Tracey L Bonfield, Morgan T Sutton, David R Fletcher, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 26, 2019
Inactivation of CFTR by CRISPR/Cas9 alters transcriptional regulation of inflammatory pathways and other networks
Shuyu Hao, Erica A Roesch, Aura Perez, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 22, 2022
A phase I study assessing the safety and tolerability of allogeneic mesenchymal stem cell infusion in adults with cystic fibrosis
Erica A Roesch, Tracey L Bonfield, Hillard M Lazarus, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Pediatric Pulmonology
|
September 30, 2017
Powerful tools for genetic modification: Advances in gene editing
Erica A Roesch, Mitchell L Drumm
Expert Review of Respiratory Medicine
|
March 23, 2022
The use of tobramycin for Pseudomonas aeruginosa: a review
Stanley B Fiel, Erica A Roesch
Pediatric Pulmonology
|
July 13, 2018
Inflammation in cystic fibrosis: An update
Erica A Roesch, David P Nichols, James F Chmiel
Current Opinion in Pulmonary Medicine
|
August 23, 2023
Chronic daily respiratory care needs in people with cystic fibrosis treated with highly effective cystic fibrosis transmembrane conductance regulator modulators
Katherine E Wajda, Erica A Roesch, Alex H Gifford
Expert Review of Respiratory Medicine
|
August 23, 2024
The continuing need for dornase alfa for extracellular airway DNA hydrolysis in the era of CFTR modulators
Erica A Roesch, Abdelkader Rahmaoui, Robert A Lazarus, et al.
Frontiers in Pediatrics
|
November 7, 2024
Case Report: A delicate equilibrium of exocrine pancreatic recovery and hepatotoxicity with elexacaftor/tezacaftor/ivacaftor therapy in a pediatric patient with cystic fibrosis
Michael P Coughlin, Senthilkumar Sankararaman, Erica A Roesch, et al.
Pharmaceuticals (Basel, Switzerland)
|
June 1, 2023
Human Mesenchymal Stem Cell (hMSC) Donor Potency Selection for the "First in Cystic Fibrosis" Phase I Clinical Trial (CEASE-CF)
Tracey L Bonfield, Morgan T Sutton, David R Fletcher, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
May 26, 2019
Inactivation of CFTR by CRISPR/Cas9 alters transcriptional regulation of inflammatory pathways and other networks
Shuyu Hao, Erica A Roesch, Aura Perez, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
December 22, 2022
A phase I study assessing the safety and tolerability of allogeneic mesenchymal stem cell infusion in adults with cystic fibrosis
Erica A Roesch, Tracey L Bonfield, Hillard M Lazarus, et al.
Page
of 1