Browsing publications by Dr Joanna Elson

Newcastle AuthorsTitleYearFull text
Dr Ilse-Sanet Pienaar
Dr Joanna Elson
Alex Bury
An animal model mimicking pedunculopontine nucleus cholinergic degeneration in Parkinson's disease2015
Dr Ilse-Sanet Pienaar
Dr Joanna Elson
Professor Raj Kalaria
Deep-brain stimulation associates with improved microvascular integrity in the subthalamic nucleus in Parkinson's disease2015
Dr Ilse-Sanet Pienaar
Dr Joanna Elson
Professor Raj Kalaria
Deep-brain stimulation associates with improved microvascular integrity in the subthalamic nucleus in Parkinson's disease2015
Dr Joanna Elson
Dr Paul Smith
Heterologous Inferential Analysis (HIA) as a Method to Understand the Role of Mitochondrial rRNA Mutations in Pathogenesis2015
Dr Grainne Gorman
Dr Joanna Elson
Jane Newman
Dr Brendan Payne
Dr Bobby McFarland
et al.
Perceived fatigue is highly prevalent and debilitating in patients with mitochondrial disease2015
Dr Laura Greaves
Marco Nooteboom
Dr Joanna Elson
Dr Helen Tuppen
Geoffrey Taylor
et al.
Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing2014
Dr Joanna Elson
Mark Cadogan
Dr Roger Whittaker
Professor Michael Trenell
Professor Rita Horvath
et al.
Initial development and validation of a mitochondrial disease quality of life scale2013
Dr Ilse-Sanet Pienaar
Dr Joanna Elson
Dr Claudia Racca
Dr Glyn Nelson
Professor Doug Turnbull
et al.
Mitochondrial Abnormality Associates with Type-Specific Neuronal Loss and Cell Morphology Changes in the Pedunculopontine Nucleus in Parkinson Disease2013
Dr Paul Smith
Dr Joanna Elson
Dr Laura Greaves
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
The role of the mitochondrial ribosome in human disease: Searching for mutations in 12S mitochondrial rRNA with high disruptive potential2013
Dr John Yarham
Dr Bobby McFarland
Professor Robert Taylor
Dr Joanna Elson
A proposed consensus panel of organisms for determining evolutionary conservation of mt-tRNA point mutations2012
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