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Mark David McGregor Davis

Researcher at Monash University

Publications -  157
Citations -  6851

Mark David McGregor Davis is an academic researcher from Monash University. The author has contributed to research in topics: Acquired immunodeficiency syndrome (AIDS) & Public health. The author has an hindex of 36, co-authored 150 publications receiving 6356 citations. Previous affiliations of Mark David McGregor Davis include University College London & University of Queensland.

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Australia’s pandemic influenza ‘Protect’ phase: emerging out of the fog of pandemic

TL;DR: Examination of preparedness efforts established in anticipation of a catastrophic threat were reconfigured during the Australian 2009 (H1N1) pandemic influenza to indicate that classical population health efforts interrupted not only the vision of catastrophe embedded within the plans, but the actual plans and their implementation, forcing the public health response in a new direction.
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Investigating Understandings of Antibiotics and Antimicrobial Resistance in Diverse Ethnic Communities in Australia: Findings from a Qualitative Study.

TL;DR: There was poor understanding of AMR, even among informants being treated for AMR infections, and more attention needs to be given to migrant communities who are vulnerable to the development, transmission and infection with resistant bacteria to inform future interventions.

"Is it Going to be Real?" Narrative and Media on a Pandemic

TL;DR: The authors examine the narrative-media nexus as it relates to pandemics and examine the ways in which narrative is appropriated to communicate a pandemic's temporal and affective qualities, and how, in the circumstances of an actual outbreak, publics are invited to consider themselves as the ideal, "alert, but not alarmed" subjects of the pandemic storyworld.
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Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series.

TL;DR: Five patients with mutations in HSPB1 are presented who presented with a range of clinical phenotypes related to different patterns of motor neuron dysfunction and three of these mutations have not been previously reported are described.