Aoife P. Kiely
Queen Square Brain Bank For Neurological Disorders, UCL Queen Square Institute Of Neurology
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 9 publications
Immunohistochemical and Molecular Investigations Show Alteration in the Inflammatory Profile of Multiple System Atrophy Brain.
Journal: Journal of neuropathology and experimental neurology
Published: June 01, 2018
Exploring the putative role of kallikrein-6, calpain-1 and cathepsin-D in the proteolytic degradation of α-synuclein in multiple system atrophy.
Journal: Neuropathology and applied neurobiology
Published: May 15, 2018
Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients.
Journal: PloS one
Published: September 21, 2015
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation.
Journal: Molecular neurodegeneration
Published: May 22, 2015
Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions.
Journal: Acta neuropathologica communications
Published: September 18, 2014
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.
Journal: JAMA neurology
Published: July 09, 2014
The novel Parkinson's disease linked mutation G51D attenuates in vitro aggregation and membrane binding of α-synuclein, and enhances its secretion and nuclear localization in cells.
Journal: Human molecular genetics
Published: April 15, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026