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Michelle Barnes

Researcher at University of New South Wales

Publications -  6
Citations -  678

Michelle Barnes is an academic researcher from University of New South Wales. The author has contributed to research in topics: Vaccination & Immunogenicity. The author has an hindex of 5, co-authored 6 publications receiving 494 citations.

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The role of pneumonia and secondary bacterial infection in fatal and serious outcomes of pandemic influenza a(H1N1)pdm09.

TL;DR: It was found that few studies of the 2009 influenza pandemic reported on bacterial complications and testing, and secondary bacterial infection was identified in almost one in four patients, with Streptococcus pneumoniae the most common bacteria identified.
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Acute myocardial infarction and influenza: a meta-analysis of case–control studies

TL;DR: The estimated vaccine effectiveness against AMI was comparable with the efficacy of currently accepted therapies for secondary prevention of AMI from clinical trial data, and a large-scale randomised controlled trial is needed to provide robust evidence of the protective effect of influenza vaccination on AMI.
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Influenza vaccine as a coronary intervention for prevention of myocardial infarction

TL;DR: Influenza vaccine should be considered as an integral part of CVD management and prevention and incorporated into routine CVD prevention in patient care requires a clinical practice paradigm change.
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Persistence of Ebola virus in various body fluids during convalescence: evidence and implications for disease transmission and control.

TL;DR: There is a need for more research on persistence, and a uniform approach to infection control guidelines in convalescence, as available evidence suggests that EBOV can persist in some body fluids after clinical recovery and clearance of virus from the blood.
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Immunogenicity and persistence of immunity of a quadrivalent Human Papillomavirus (HPV) vaccine in immunocompromised children.

TL;DR: Immunosuppressed children had an adequate immunogenic response to Quadrivalent HPV vaccine regardless of age and the cause of immunosuppression, so early vaccination and optimal scheduling should be further studied in such children.