User profiles for Thomas E. Cope
Thomas E CopeConsultant Neurologist, University of Cambridge Verified email at cam.ac.uk Cited by 2901 |
[PDF][PDF] The brain basis for misophonia
Misophonia is an affective sound-processing disorder characterized by the experience of
strong negative emotions (anger and anxiety) in response to everyday sounds, such as those …
strong negative emotions (anger and anxiety) in response to everyday sounds, such as those …
[HTML][HTML] Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Background Frontotemporal dementia is a heterogenous neurodegenerative disorder, with
about a third of cases being genetic. Most of this genetic component is accounted for by …
about a third of cases being genetic. Most of this genetic component is accounted for by …
18F-AV-1451 positron emission tomography in Alzheimer's disease and progressive supranuclear palsy
…, D Williamson, RJ Borchert, S Sami, TE Cope… - Brain, 2017 - academic.oup.com
The ability to assess the distribution and extent of tau pathology in Alzheimer’s disease and
progressive supranuclear palsy in vivo would help to develop biomarkers for these …
progressive supranuclear palsy in vivo would help to develop biomarkers for these …
Tau burden and the functional connectome in Alzheimer's disease and progressive supranuclear palsy
Alzheimer’s disease and progressive supranuclear palsy (PSP) represent neurodegenerative
tauopathies with predominantly cortical versus subcortical disease burden. In Alzheimer’s …
tauopathies with predominantly cortical versus subcortical disease burden. In Alzheimer’s …
[HTML][HTML] Evidence for causal top-down frontal contributions to predictive processes in speech perception
Perception relies on the integration of sensory information and prior expectations. Here we
show that selective neurodegeneration of human frontal speech regions results in delayed …
show that selective neurodegeneration of human frontal speech regions results in delayed …
Neuroinflammation and protein aggregation co-localize across the frontotemporal dementia spectrum
The clinical syndromes of frontotemporal dementia are clinically and neuropathologically
heterogeneous, but processes such as neuroinflammation may be common across the disease …
heterogeneous, but processes such as neuroinflammation may be common across the disease …
Microglial activation in the frontal cortex predicts cognitive decline in frontotemporal dementia
Frontotemporal dementia is clinically and neuropathologically heterogeneous, but
neuroinflammation, atrophy and cognitive impairment occur in all of its principal syndromes. Across …
neuroinflammation, atrophy and cognitive impairment occur in all of its principal syndromes. Across …
[18F] AV-1451 binding in vivo mirrors the expected distribution of TDP-43 pathology in the semantic variant of primary progressive aphasia
Introduction Semantic dementia, including the semantic variant of primary progressive
aphasia (svPPA), is strongly associated with TAR-DNA binding protein 43 (TDP-43) type C …
aphasia (svPPA), is strongly associated with TAR-DNA binding protein 43 (TDP-43) type C …
[HTML][HTML] The basal ganglia in perceptual timing: timing performance in Multiple System Atrophy and Huntington's disease
The timing of perceptual events depends on an anatomically and functionally connected
network comprising basal ganglia, cerebellum, pre-frontal cortex and supplementary motor area…
network comprising basal ganglia, cerebellum, pre-frontal cortex and supplementary motor area…
Synaptic Loss in Frontotemporal Dementia Revealed by [11C]UCB‐J Positron Emission Tomography
Objective Synaptic loss is an early feature of neurodegenerative disease models, and is
severe in post mortem clinical studies, including frontotemporal dementia. Positron emission …
severe in post mortem clinical studies, including frontotemporal dementia. Positron emission …