Ronald Druyeh

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 10 publications

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases.

Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseases.

Journal: Molecular psychiatry

Published: July 27, 2020

ApoE4 lowers age at onset in patients with frontotemporal dementia and tauopathy independent of amyloid-β copathology.

ApoE4 lowers age at onset in patients with frontotemporal dementia and tauopathy independent of amyloid-β copathology.

Journal: Alzheimer's & dementia (Amsterdam, Netherlands)

Published: April 06, 2019

Longitudinal measurement of serum neurofilament light in presymptomatic familial Alzheimer's disease.

Longitudinal measurement of serum neurofilament light in presymptomatic familial Alzheimer's disease.

Journal: Alzheimer's research & therapy

Published: November 04, 2018

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series.

Predictors for a dementia gene mutation based on gene-panel next-generation sequencing of a large dementia referral series.

Journal: Molecular psychiatry

Published: January 26, 2018

Serum neurofilament light in familial Alzheimer disease: A marker of early neurodegeneration.

Serum neurofilament light in familial Alzheimer disease: A marker of early neurodegeneration.

Journal: Neurology

Published: April 14, 2017

Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia.

Serum neurofilament light chain protein is a measure of disease intensity in frontotemporal dementia.

Journal: Neurology

Published: March 05, 2016

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease.

Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease.

Journal: JAMA neurology

Published: February 24, 2016

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.

Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.

Journal: BMC medical genetics

Published: September 16, 2015

Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD.

Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD.

Journal: Neurobiology of aging

Published: October 21, 2014

Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases.

Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases.

Journal: Acta neuropathologica communications

Published: March 12, 2013

Showing 1-10 of 10

Last Updated: 09/26/2026