Dimitrios I. Sideris

ORCID: 0000-0001-5233-8845
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About
Contact & Profiles
Research Areas
  • Alzheimer's disease research and treatments
  • Dementia and Cognitive Impairment Research
  • Parkinson's Disease Mechanisms and Treatments
  • biodegradable polymer synthesis and properties
  • Neurological disorders and treatments
  • S100 Proteins and Annexins
  • Tryptophan and brain disorders
  • Neurological Disorders and Treatments
  • Amyotrophic Lateral Sclerosis Research
  • Neuroinflammation and Neurodegeneration Mechanisms

University of Cambridge
2019-2022

AstraZeneca (United Kingdom)
2021

University of Edinburgh
2017

In addition to motor neurone degeneration, up 50% of amyotrophic lateral sclerosis (ALS) patients present with cognitive decline. Understanding the neurobiological changes underlying these deficits is critical, as cognitively impaired exhibit a shorter survival time from symptom onset. Given pathogenic role synapse loss in other neurodegenerative diseases which decline apparent, such Alzheimer's disease, we aimed assess synaptic integrity ALS brain. Here, have applied unique combination...

10.1007/s00401-017-1797-4 article EN cc-by Acta Neuropathologica 2017-12-22

Soluble aggregates of amyloid-β (Aβ) have been associated with neuronal and synaptic loss in Alzheimer's disease (AD). However, despite significant recent progress, the mechanisms by which these aggregated species contribute to progression are not fully determined. As analysis human cerebrospinal fluid (CSF) provides an accessible window into molecular changes progression, we characterised soluble present CSF samples from individuals AD, mild cognitive impairment (MCI) healthy controls using...

10.1186/s40478-019-0777-4 article EN cc-by Acta Neuropathologica Communications 2019-07-26

Protein aggregation likely plays a key role in the initiation and spreading of Alzheimer's disease pathology through brain. Soluble aggregates amyloid beta are believed to play this process. However, present humans still poorly characterized due lack suitable methods required for characterizing low concentration heterogeneous present. We have used variety biophysical characterize human brains at Braak stage III. find soluble beta-containing all regions brain up 200 nm length, capable causing...

10.1093/braincomms/fcab147 article EN cc-by Brain Communications 2021-01-01

Abstract Soluble aggregates of amyloid-β (Aβ) have been associated with neuronal and synaptic loss in Alzheimer’s disease (AD). However, despite significant recent progress, the mechanisms by which these aggregated species contribute to progression are not fully determined. As analysis human cerebrospinal fluid (CSF) provides an accessible window into molecular changes progression, we studied soluble Aβ present CSF samples from individuals AD, mild cognitive impairment (MCI) healthy...

10.1101/600346 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2019-04-05
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