Showing results (11-20 of 67) with videos related to
Sort By:
Pageof 7
Clinical Chemistry and Laboratory Medicine|March 15, 2003
Modified method to measure nasal potential differenceTeresinha Leal, Jean Lebacq, Patrick Lebecque, et al.Plos One|November 9, 2013
Correction of chloride transport and mislocalization of CFTR protein by vardenafil in the gastrointestinal tract of cystic fibrosis miceBarbara Dhooghe, Sabrina Noël, Caroline Bouzin, et al.Frontiers in Pharmacology|May 14, 2021
On the Corner of Models and Cure: Gene Editing in Cystic FibrosisMarjolein Ensinck, Angélique Mottais, Claire Detry, et al.Respiratory Medicine and Research|September 21, 2023
Comparison of amikacin lung delivery between AKITA® and eFlow rapid® nebulizers in healthy controls and patients with CF: A randomized cross-over trialAnne-Sophie Aubriot, Guillaume Maerckx, Teresinha Leal, et al.Physiotherapy|April 8, 2025
Impact of adding positive expiratory pressure to nebulisation on drug delivery: a comparative studyAnne-Sophie Aubriot, Teresinha Leal, Jean-Christophe Dubus, et al.Journal of Aerosol Medicine and Pulmonary Drug Delivery|October 21, 2010
Delivery efficacy of a vibrating mesh nebulizer and a jet nebulizer under different configurationsLaurent Pitance, Laurent Vecellio, Teresinha Leal, et al.Biology Open|June 21, 2015
Resveratrol increases F508del-CFTR dependent salivary secretion in cystic fibrosis miceBarbara Dhooghe, Charlotte Bouckaert, Arnaud Capron, et al.Journal of Aerosol Medicine and Pulmonary Drug Delivery|February 25, 2016
Influence of Tracheostomy on Lung Deposition in Spontaneously Breathing PatientsLaurent Pitance, Grégory Reychler, Laurent Vecellio, et al.Pflugers Archiv : European Journal of Physiology|September 20, 2011
Decreased renal accumulation of aminoglycoside reflects defective receptor-mediated endocytosis in cystic fibrosis and Dent's diseaseClaudia Raggi, Kunio Fujiwara, Teresinha Leal, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 23, 2006
Towards zero prevalence of chronic Pseudomonas aeruginosa infection in children with cystic fibrosisPatrick Lebecque, Teresinha Leal, Katia Zylberberg, et al.Pageof 7