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The American Journal of Sports Medicine|August 3, 2014
Incidence and trends of anterior cruciate ligament reconstruction in the United StatesNathan A Mall, Peter N Chalmers, Mario Moric, et al.Frontiers in Immunology|March 3, 2020
<i>Pseudomonas aeruginosa</i> Modulates the Antiviral Response of Bronchial Epithelial CellsMichael Sörensen, Julia Kantorek, Lauren Byrnes, et al.Frontiers in Pharmacology|May 8, 2023
Effects of elexacaftor/tezacaftor/ivacaftor therapy on mental health of patients with cystic fibrosisLinus Piehler, Ralf Thalemann, Christine Lehmann, et al.Frontiers in Pharmacology|March 11, 2025
Intestinal current measurement detects age-dependent differences in CFTR function in rectal epitheliumSimon Y Graeber, Olaf Sommerburg, Yin Yu, et al.European Respiratory Review : an Official Journal of the European Respiratory Society|September 4, 2024
A systematic literature review of the clinical and socioeconomic burden of bronchiectasisJames D Chalmers, Marcus A Mall, Pamela J McShane, et al.JCI Insight|April 22, 2025
The potentiator ivacaftor is essential for pharmacological restoration of F508del-CFTR function and mucociliary clearance in cystic fibrosisAnita Balázs, Tihomir Rubil, Christine K Wong, et al.Mediators of Inflammation|February 18, 2015
Supplementation with red palm oil increases β-carotene and vitamin A blood levels in patients with cystic fibrosisOlaf Sommerburg, Silke De Spirt, Annett Mattern, et al.American Journal of Respiratory and Critical Care Medicine|October 14, 2008
Preventive but not late amiloride therapy reduces morbidity and mortality of lung disease in betaENaC-overexpressing miceZhe Zhou, Diana Treis, Susanne C Schubert, et al.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|April 14, 2016
Imaging of Cystic Fibrosis Lung Disease and Clinical InterpretationM O Wielpütz, M Eichinger, J Biederer, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 17, 2017
Three-center feasibility of lung clearance index in infants and preschool children with cystic fibrosis and other lung diseasesMirjam Stahl, Simon Y Graeber, Cornelia Joachim, et al.Pageof 38