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Scientific Reports|July 25, 2020
Author Correction: Increased susceptibility of airway epithelial cells from ataxia-telangiectasia to S. pneumoniae infection due to oxidative damage and impaired innate immunityAbrey J Yeo, Anna Henningham, Emmanuelle Fantino, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 23, 2020
Total bacterial load, inflammation, and structural lung disease in paediatric cystic fibrosisSteven L Taylor, Lex E X Leong, Kerry L Ivey, et al.Journal of Clinical Microbiology|September 20, 2013
Factors influencing acquisition of Burkholderia cepacia complex organisms in patients with cystic fibrosisKay A Ramsay, Claire A Butler, Stuart Paynter, et al.Journal of Medical Microbiology|October 22, 2004
Rapid genotyping of Pseudomonas aeruginosa isolates harboured by adult and paediatric patients with cystic fibrosis using repetitive-element-based PCR assaysMelanie W Syrmis, Mark R O'Carroll, Theo P Sloots, et al.British Journal of Psychology (London, England : 1953)|November 26, 2008
Impact of simulated visual impairment on the cognitive test performance of young adultsJoanne M Wood, Alex Chaparro, Kaarin J Anstey, et al.European Journal of Clinical Nutrition|June 29, 2004
The use of air displacement plethysmography in children and adolescents with cystic fibrosisA J Murphy, H M Buntain, J C H Wong, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 7, 2022
Neutrophil respiratory burst activity is not exaggerated in cystic fibrosisDean Kelk, Jayden Logan, Isabella Andersen, et al.Scientific Reports|February 24, 2019
Increased susceptibility of airway epithelial cells from ataxia-telangiectasia to S. pneumoniae infection due to oxidative damage and impaired innate immunityAbrey J Yeo, Anna Henningham, Emmanuelle Fantino, et al.Lipids|December 2, 1999
Effects of gamma-linolenic acid and docosahexaenoic acid in formulae on brain fatty acid composition in artificially reared ratsG R Ward, Y S Huang, H C Xing, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 28, 2017
Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftorPatrick A Flume, Claire E Wainwright, D Elizabeth Tullis, et al.Pageof 20