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The Lancet. Infectious Diseases|June 21, 2016
Antibiotic duration and timing of the switch from intravenous to oral route for bacterial infections in children: systematic review and guidelinesBrendan J McMullan, David Andresen, Christopher C Blyth, et al.The Medical Journal of Australia|February 28, 2021
Otitis media guidelines for Australian Aboriginal and Torres Strait Islander children: summary of recommendationsAmanda J Leach, Peter S Morris, Harvey Lc Coates, et al.Journal of Public Health (Oxford, England)|August 12, 2025
Nudging towards COVID-19 and influenza vaccination in children with medically at-risk conditionsBing Wang, Prabha Andraweera, Margie Danchin, et al.Clinical Medicine (London, England)|April 20, 2024
Addressing ethnic disparities in neurological research in the United Kingdom: An example from the prospective multicentre COVID-19 Clinical Neuroscience StudyDaniel J van Wamelen, Silvia Rota, Monika Hartmann, et al.Journal of Clinical Immunology|July 5, 2023
Infection and Vaccine Induced Spike Antibody Responses Against SARS-CoV-2 Variants of Concern in COVID-19-Naïve Children and AdultsAleha Pillay, Avani Yeola, Fiona Tea, et al.Annals of Neurology|March 11, 2021
Mitochondrial DNA Analysis from Exome Sequencing Data Improves Diagnostic Yield in Neurological DiseasesOlivia V Poole, Chiara Pizzamiglio, David Murphy, et al.NPJ Vaccines|July 16, 2025
Surveillance and follow up outcomes of myocarditis after mRNA COVID-19 vaccination in AustraliaLucy Deng, Amanda Van Eldik, Megan O'Moore, et al.Annals of Neurology|April 5, 2016
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesConceição Bettencourt, Davina Hensman-Moss, Michael Flower, et al.Vaccine|July 10, 2025
Randomised controlled trials of behavioural nudges delivered through text messages to increase influenza and COVID-19 vaccine uptake among pregnant women (EPIC study) in AustraliaPrabha H Andraweera, Bing Wang, Margie Danchin, et al.Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.Pageof 32