Lee Darwent

33 Cleveland Street, W1W 7FF
London, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 25 publications

Performance of Alzheimer Disease Plasma Biomarkers in Patients With Prion Diseases.

Performance of Alzheimer Disease Plasma Biomarkers in Patients With Prion Diseases.

Journal: Neurology
Published: July 13, 2026

Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157.

Inherited prion disease caused by a novel frameshift mutation of PRNP resulting in protein truncation at codon 157.

Journal: Journal of Alzheimer's disease : JAD
Published: July 04, 2025

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features.

PRNP E146G mutation inherited prion disease: distinctive clinical, pathological and fluid biomarker features.

Journal: Journal of neurology
Published: November 28, 2024

Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes.

Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes.

Journal: Brain : a journal of neurology
Published: July 21, 2024

Genome wide association study of clinical duration and age at onset of sporadic CJD.

Genome wide association study of clinical duration and age at onset of sporadic CJD.

Journal: PloS one
Published: February 21, 2024

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease.

Seed amplification and neurodegeneration marker trajectories in individuals at risk of prion disease.

Journal: Brain : a journal of neurology
Published: November 09, 2022

DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt-Jakob disease.

DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt-Jakob disease.

Journal: Acta neuropathologica
Published: June 15, 2022

Estimation of the number of inherited prion disease mutation carriers in the UK.

Estimation of the number of inherited prion disease mutation carriers in the UK.

Journal: European journal of human genetics : EJHG
Published: March 25, 2022

Prion protein gene mutation detection using long-read Nanopore sequencing.

Prion protein gene mutation detection using long-read Nanopore sequencing.

Journal: Scientific reports
Published: February 17, 2022

Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt-Jakob disease: evaluation of a first-in-human treatment programme.

Prion protein monoclonal antibody (PRN100) therapy for Creutzfeldt-Jakob disease: evaluation of a first-in-human treatment programme.

Journal: The Lancet. Neurology
Published: October 22, 2021

Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease.

Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease.

Journal: BMC neurology
Published: November 19, 2020

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies.

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies.

Journal: Acta neuropathologica communications
Published: November 20, 2019
Showing 1-12 of 25

Last Updated: 09/26/2026