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Physics and Imaging in Radiation Oncology|November 30, 2023
Development of a comprehensive cardiac atlas on a 1.5 Tesla Magnetic Resonance Linear AcceleratorAronne M Schottstaedt, Eric S Paulson, Jason C Rubenstein, et al.Diabetes|August 7, 2016
Reduced β-Cell Secretory Capacity in Pancreatic-Insufficient, but Not Pancreatic-Sufficient, Cystic Fibrosis Despite Normal Glucose ToleranceSaba Sheikh, Lalitha Gudipaty, Diva D De Leon, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 5, 2017
Sexual and reproductive health behaviors and experiences reported by young women with cystic fibrosisTraci M Kazmerski, Gregory S Sawicki, Elizabeth Miller, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 4, 2017
Sexual and reproductive health care utilization and preferences reported by young women with cystic fibrosisTraci M Kazmerski, Gregory S Sawicki, Elizabeth Miller, et al.Microorganisms|June 2, 2021
Microbial Sharing between Pediatric Patients and Therapy Dogs during Hospital Animal-Assisted Intervention ProgramsKathryn R Dalton, Kathy Ruble, Laurel E Redding, et al.International Journal of Biomedical Imaging|May 31, 2021
Value CMR: Towards a Comprehensive, Rapid, Cost-Effective Cardiovascular Magnetic Resonance ImagingEl-Sayed H Ibrahim, Luba Frank, Dhiraj Baruah, et al.Diabetes|July 7, 2022
Effects of GLP-1 and GIP on Islet Function in Glucose-Intolerant, Pancreatic-Insufficient Cystic FibrosisSarah C Nyirjesy, Amy J Peleckis, Jack N Eiel, et al.Thorax|June 11, 2013
Phase II studies of nebulised Arikace in CF patients with Pseudomonas aeruginosa infectionJ P Clancy, L Dupont, M W Konstan, et al.Journal of Molecular and Cellular Cardiology|October 15, 2023
Profibrotic COVID-19 subphenotype exhibits enhanced localized ER-dependent HSP47+ expression in cardiac myofibroblasts in situElizabeth R Jacobs, Gracious R Ross, Nathan Padilla, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 18, 2014
Long-term treatment with oral N-acetylcysteine: affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trialC Conrad, J Lymp, V Thompson, et al.Pageof 13