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IEEE Journal of Translational Engineering in Health and Medicine|February 26, 2019
Improving Detection of Rapid Cystic Fibrosis Disease Progression-Early Translation of a Predictive Algorithm Into a Point-of-Care ToolRhonda D Szczesniak, Cole Brokamp, Weiji Su, et al.
Frontiers in Physiology|January 4, 2021
A Novel G542X CFTR Rat Model of Cystic Fibrosis Is Sensitive to Nonsense Mediated DecayJyoti Sharma, Joseph Abbott, Lauren Klaskala, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2020
Tobacco smoke exposure limits the therapeutic benefit of tezacaftor/ivacaftor in pediatric patients with cystic fibrosisElizabeth Baker, William T Harris, Steven M Rowe, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 16, 2015
Electronic monitoring reveals highly variable adherence patterns in patients prescribed ivacaftorChristopher M Siracusa, Jamie Ryan, Lisa Burns, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 11, 2014
Daily serum creatinine monitoring promotes earlier detection of acute kidney injury in children and adolescents with cystic fibrosisKevin J Downes, Marepalli B Rao, Laurie Kahill, et al.
American Journal of Respiratory and Critical Care Medicine|April 16, 2017
Phenotypes of Rapid Cystic Fibrosis Lung Disease Progression during Adolescence and Young AdulthoodRhonda D Szczesniak, Dan Li, Weiji Su, et al.
Plos One|September 17, 2013
Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR functionJohn P Clancy, Rhonda D Szczesniak, Melissa A Ashlock, et al.
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