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Pediatric Pulmonology|March 1, 2018
Sensitivity of ivacaftor to drug-drug interactions with rifampin, a cytochrome P450 3A4 inducerJennifer S Guimbellot, Edward P Acosta, Steven M RoweClinics in Chest Medicine|November 7, 2022
Novel Applications of Biomarkers and Personalized Medicine in Cystic FibrosisJennifer S Guimbellot, David P Nichols, John J BrewingtonPediatric Pulmonology|May 24, 2018
Potential pathogenicity of Inquilinus limosus in a pediatric patient with cystic fibrosisT Spencer Poore, Isabel Virella-Lowell, Jennifer S GuimbellotJournal of Visualized Experiments : Jove|January 3, 2022
Culture and Imaging of Human Nasal Epithelial OrganoidsZhongyu Liu, Justin D Anderson, Jennifer Natt, et al.Pediatric Pulmonology|August 21, 2024
Literary evidence of the impact of nonbiological risk factors on CRMS/CFSPID: A scoping reviewNatalie R Rose, S Garrison Dabbs, Emma C O'Hagan, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|May 19, 2021
CFTR function and clinical response to modulators parallel nasal epithelial organoid swellingJustin D Anderson, Zhongyu Liu, L Victoria Odom, et al.The European Respiratory Journal|July 2, 2026
Unlocking growth potential: Ivacaftor therapy and developmental gains in lung and height in a cohort study of children and young adults with cystic fibrosisJennifer S Guimbellot, Elizabeth Baker, Ashritha Chalamalla, et al.Pediatric Pulmonology|March 8, 2026
Assessing Dietary Patterns and Composition Among Adults With Cystic Fibrosis Taking Highly Effective Modulator TherapyJulianna Bailey, Natalie R Rose, Ashritha R Chalamalla, et al.Pediatric Pulmonology|February 1, 2023
Electronic screening for unmet social needs in a pediatric pulmonary clinic: Acceptability and associations with health outcomesGabriela R Oates, Lindsay Lock, Valerie Tarn, et al.Frontiers in Pediatrics|March 27, 2023
Outcomes of children with cystic fibrosis screen positive, inconclusive diagnosis/CFTR related metabolic syndromeMohini A Gunnett, Elizabeth Baker, Cathy Mims, et al.Pageof 4