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Pediatric Pulmonology|December 1, 2023
Clinical and genetic risk factors for cystic fibrosis-related liver disease in Egyptian CF children: A single-center experienceAmel El-Faramawy, Samya Z Nasr, Mohamed M S Al Emam, et al.
Clinics in Chest Medicine|November 7, 2022
Transitions of Care in Cystic FibrosisEunice M M DeFilippo, Jaideep S Talwalkar, Zachary M Harris, et al.
International Journal of Biological Macromolecules|September 18, 2020
Synthesis and characterization of chitosan-pyrazoloquinoxaline Schiff bases for Cr (VI) removal from wastewaterMohammed Elhag, Huda E Abdelwahab, Mohamed A Mostafa, et al.
Frontiers in Pediatrics|January 31, 2022
Assessing the Utility of an Outpatient Exercise Program for Children With Cystic Fibrosis: A Quality Improvement ProjectDionne Adair, Ahmad Hider, Amy G Filbrun, et al.
Global Pediatric Health|June 24, 2016
Improving the Rate of Sufficient Sweat Collected in Infants Referred for Sweat Testing in MichiganIbrahim Abdulhamid, Mary Kleyn, Carrie Langbo, et al.
Pediatric Pulmonology|August 10, 2020
Quality improvement initiative to improve pulmonary function in pediatric cystic fibrosis patientsAmy G Filbrun, Catherine Enochs, Lindsay Caverly, et al.
American Journal of Respiratory and Critical Care Medicine|March 1, 1995
Continuous versus intermittent nebulized terbutaline: plasma levels and effectsF W Moler, C E Johnson, C Van Laanen, et al.
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