Alexander H. Peden

Edinburgh, SCT, United Kingdom

Last Updated: 09/26/2026

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Found 14 publications

Enhanced Creutzfeldt-Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease.

Enhanced Creutzfeldt-Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease.

Journal: Brain pathology (Zurich, Switzerland)
Published: August 16, 2023

Variant CJD: Reflections a Quarter of a Century on.

Variant CJD: Reflections a Quarter of a Century on.

Journal: Pathogens (Basel, Switzerland)
Published: September 23, 2021

Understanding Intra-Species and Inter-Species Prion Conversion and Zoonotic Potential Using Protein Misfolding Cyclic Amplification.

Understanding Intra-Species and Inter-Species Prion Conversion and Zoonotic Potential Using Protein Misfolding Cyclic Amplification.

Journal: Frontiers in aging neuroscience
Published: May 28, 2021

Study protocol for enhanced CJD surveillance in the 65+ years population group in Scotland: an observational neuropathological screening study of banked brain tissue donations for evidence of prion disease.

Study protocol for enhanced CJD surveillance in the 65+ years population group in Scotland: an observational neuropathological screening study of banked brain tissue donations for evidence of prion disease.

Journal: BMJ open
Published: October 31, 2019

Epitope mapping of the protease resistant products of RT-QuIC does not allow the discrimination of sCJD subtypes.

Epitope mapping of the protease resistant products of RT-QuIC does not allow the discrimination of sCJD subtypes.

Journal: PloS one
Published: April 04, 2019

Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK.

Amyloid-β accumulation in the CNS in human growth hormone recipients in the UK.

Journal: Acta neuropathologica
Published: February 15, 2017

UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches.

UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches.

Journal: Acta neuropathologica
Published: September 10, 2016

Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.

Variably protease-sensitive prionopathy, a unique prion variant with inefficient transmission properties.

Journal: Emerging infectious diseases
Published: November 25, 2014

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease.

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease.

Journal: Acta neuropathologica communications
Published: September 11, 2014

Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?

Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?

Journal: Acta neuropathologica communications
Published: October 29, 2013

Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease.

Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease.

Journal: Annals of neurology
Published: August 29, 2012

Molecular pathology in neurodegenerative diseases.

Molecular pathology in neurodegenerative diseases.

Journal: Current drug targets
Published: February 15, 2012
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Last Updated: 09/26/2026