Matthew T. Bishop

Crewe Road
Edinburgh, SCT EH42XU, United Kingdom

Last Updated: 09/26/2026

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Found 11 publications

Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.

Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.

Journal: Brain : a journal of neurology

Published: November 14, 2018

Tapia syndrome: an unusual complication following posterior cervical spine surgery.

Tapia syndrome: an unusual complication following posterior cervical spine surgery.

Journal: British journal of neurosurgery

Published: April 20, 2017

A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.

A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk.

Journal: PloS one

Published: January 12, 2015

Gerstmann-Straüssler-Scheinker disease: novel PRNP mutation and VGKC-complex antibodies.

Gerstmann-Straüssler-Scheinker disease: novel PRNP mutation and VGKC-complex antibodies.

Journal: Neurology

Published: May 13, 2014

Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.

Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease.

Journal: BMC medical genetics

Published: March 29, 2013

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.

Journal: Brain : a journal of neurology

Published: March 02, 2013

Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countries.

Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countries.

Journal: Emerging infectious diseases

Published: September 29, 2012

MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.

MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.

Journal: Brain pathology (Zurich, Switzerland)

Published: February 01, 2012

Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.

Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects.

Journal: PloS one

Published: December 02, 2011

PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.

PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.

Journal: BMC medical genetics

Published: April 27, 2009

Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease.

Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease.

Journal: BMC medical genetics

Published: December 13, 2007

Showing 1-11 of 11

Last Updated: 09/26/2026