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Search results (71)

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Compartment-specific correlation of pathological α-synuclein in prodromal Parkinson's disease

Röttgen S. et al, (2026), Parkinsonism & Related Disorders, 144, 108178 - 108178

Palindrome-mediated 16p13.3 triplications cause a recognizable neurodegenerative disorder with ataxia.

Fasham J. et al, (2026), Am J Hum Genet, 113, 221 - 233

Serum p‐tau217 Is a Prognostic Indicator of Cognitive Impairment in Idiopathic REM Sleep Behavior Disorder

Yan S. et al, (2025), Annals of Neurology

In vivo validation of novel non-invasive PHP.eB AAVs as a potential therapeutic approach for alpha-synucleinopathies.

Fouka M. et al, (2025), Acta Neuropathol Commun, 13

Decade‐Long Prodrome on Neuroimaging: Unique Insight into Probable Corticobasal Degeneration

Tai XY. et al, (2025), Movement Disorders, 40, 1727 - 1729

Treatment Selection and Prioritization for the EJS ACT‐PD MAMS Trial Platform

Gonzalez‐Robles C. et al, (2025), Movement Disorders, 40, 1307 - 1317

Working memory filtering at encoding and maintenance in healthy ageing, Alzheimer’s and Parkinson’s disease

Toniolo S. et al, (2025), Scientific Reports, 15

Single extracellular vesicle detection assay identifies membrane-associated α-synuclein as an early-stage biomarker in Parkinson’s disease

Yan S. et al, (2025), Cell Reports Medicine, 6, 101999 - 101999

Neuronally Derived Extracellular Vesicle α-Synuclein as a Serum Biomarker for Individuals at Risk of Developing Parkinson Disease

Yan S. et al, (2024), JAMA Neurology, 81, 59 - 59

Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design

Tolonen JP. et al, (2024), Movement Disorders, 39, 141 - 151

WORKING MEMORY FILTERING AT ENCODING AND MAINTENANCE IN HEALTHY AGEING, ALZHEIMER’S AND PARKINSON’S DISEASE

Toniolo S. et al, (2024)

Normal and pathogenic variation of RFC1 repeat expansions: implications for clinical diagnosis.

Dominik N. et al, (2023), Brain, 146, 5060 - 5069

Methodological considerations in neuronal extracellular vesicle isolation for α-synuclein biomarkers

Yan S. et al, (2023), Brain, 146, e95 - e97

Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy.

Park J. et al, (2023), Genet Med, 25

Towards a multi-arm multi-stage platform trial of disease modifying approaches in Parkinson's disease.

Foltynie T. et al, (2023), Brain, 146, 2717 - 2722

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