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Expert Review of Respiratory Medicine|March 27, 2014
Hypertonic saline for cystic fibrosis: worth its salt?Jennifer L Goralski, Scott H DonaldsonRespiratory Medicine|July 12, 2014
Breathing easier: addressing the challenges of aerosolizing medications to infants and preschoolersJennifer L Goralski, Stephanie D DavisPediatric Pulmonology|September 4, 2015
Improving complex medical care while awaiting next-generation CFTR potentiators and correctors: The current pipeline of therapeuticsJennifer L Goralski, Stephanie D DavisJournal of Aerosol Medicine and Pulmonary Drug Delivery|January 31, 2014
Challenges and limitations of testing efficacy of aerosol device delivery in young childrenJennifer L Goralski, Stephanie D DavisPediatric Pulmonology|September 27, 2017
Overcoming barriers to a successful transition from pediatric to adult careJennifer L Goralski, Samya Z Nasr, Ahmet UluerTherapeutic Advances in Respiratory Disease|November 26, 2009
Intrapleural hemorrhage after administration of tPA: a case report and review of the literatureJennifer L Goralski, Philip A Bromberg, Benjamin HaithcockCurrent Opinion in Pharmacology|May 5, 2010
Osmolytes and ion transport modulators: new strategies for airway surface rehydrationJennifer L Goralski, Richard C Boucher, Brian ButtonPediatric Pulmonology|June 28, 2020
Novel imaging techniques for cystic fibrosis lung diseaseJennifer L Goralski, Neil J Stewart, Jason C WoodsClinical Therapeutics|March 14, 2026
Fetal Transplacental Therapy to Mitigate Consequences of Cystic FibrosisCharissa W Kam, Cameron J McKinzie, Jennifer L GoralskiPediatric Pulmonology|May 9, 2019
Time for a gut check: Pancreatic sufficiency resulting from CFTR modulator useRosemary Megalaa, Vani Gopalareddy, Elizabeth Champion, et al.Pageof 5