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Plos Medicine|March 2, 2018
Delays in completion and results reporting of clinical trials under the Paediatric Regulation in the European Union: A cohort studyThomas J Hwang, Paolo A Tomasi, Florence T BourgeoisPediatrics|April 16, 2014
Postmarketing trials and pediatric device approvalsThomas J Hwang, Aaron S Kesselheim, Florence T BourgeoisJAMA Pediatrics|November 20, 2018
Completion Rate and Reporting of Mandatory Pediatric Postmarketing Studies Under the US Pediatric Research Equity ActThomas J Hwang, Liat Orenstein, Aaron S Kesselheim, et al.Health Affairs (Project Hope)|February 5, 2019
Impact Of The Priority Review Voucher Program On Drug Development For Rare Pediatric DiseasesThomas J Hwang, Florence T Bourgeois, Jessica M Franklin, et al.Journal of the National Cancer Institute|October 31, 2019
Pediatric Trials for Cancer Therapies With Targets Potentially Relevant to Pediatric CancersThomas J Hwang, Liat Orenstein, Steven G DuBois, et al.Journal of the American Medical Informatics Association : JAMIA|April 28, 2020
Is it time for computable evidence synthesis?Adam G Dunn, Florence T BourgeoisPediatrics|June 5, 2003
Adult patient visits to children's hospital emergency departmentsFlorence T Bourgeois, Michael W ShannonPediatrics|March 5, 2002
Retropharyngeal cellulitis in a 5-week-old infantFlorence T Bourgeois, Michael W ShannonPediatric Emergency Care|March 14, 2007
Emergency care for children in pediatric and general emergency departmentsFlorence T Bourgeois, Michael W ShannonHealth Affairs (Project Hope)|October 5, 2020
Pediatric Drug Policies Supporting Safe And Effective Use Of Therapeutics In Children: A Systematic AnalysisMary Carmack, Thomas Hwang, Florence T BourgeoisPageof 15