Peter Rudge

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

Last Updated: 09/26/2026

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Found 49 publications

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

The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's disease.

The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer's disease.

Journal: Journal of neurogenetics

Published: January 10, 2025

Amyloid antibody therapy for early-stage Alzheimer's disease: a critical review of three recent trials.

Amyloid antibody therapy for early-stage Alzheimer's disease: a critical review of three recent trials.

Journal: Journal of neurology

Published: March 24, 2024

Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone.

Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone.

Journal: Nature medicine

Published: October 03, 2023

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

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

Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study.

Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort Study.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: March 24, 2022

Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease.

Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob disease.

Journal: Brain communications

Published: February 08, 2022

Assessing initial MRI reports for suspected CJD patients.

Assessing initial MRI reports for suspected CJD patients.

Journal: Journal of neurology

Published: January 08, 2022

Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenon.

Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenon.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: January 06, 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

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease.

Development of novel clinical examination scales for the measurement of disease severity in Creutzfeldt-Jakob disease.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: August 29, 2021

Showing 1-12 of 49

Last Updated: 09/26/2026