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Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations

Neuropathology and applied neurobiology, 2015-12, Vol.41 (7), p.858-881

2015

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Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes

Neurology, 2016-05, Vol.86 (18), p.1736-1743

2016

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Review: Fluid biomarkers in the human prion diseases

Molecular and cellular neuroscience, 2019-06, Vol.97, p.81-92

2019

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

Neurology, 2016-09, Vol.87 (13), p.1329-1336

2016

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Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

The Lancet (British edition), 2011-02, Vol.377 (9764), p.487-493

2011

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Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura

Annals of neurology, 2019-02, Vol.85 (2), p.284-290

2019

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A naturally occurring variant of the human prion protein completely prevents prion disease

Nature (London), 2015-06, Vol.522 (7557), p.478-481

2015

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The Intractable Puzzle of Sporadic Creutzfeldt-Jakob Disease in Very Young People

Neurology, 2021-10, Vol.97 (17), p.801-802

Mead, Simon

2021

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Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

Acta neuropathologica, 2013-09, Vol.126 (3), p.401-409

2013

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Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine

JAMA neurology, 2016-12, Vol.73 (12), p.1454

2016

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Prion protein gene M232R variation is probably an uncommon polymorphism rather than a pathogenic mutation

Brain (London, England : 1878), 2012-02, Vol.135 (2), p.e209-e209

2012

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

JAMA neurology, 2016-04, Vol.73 (4), p.447

2016

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The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

Brain (London, England : 1878), 2013-04, Vol.136 (Pt 4), p.1116-1127

2013

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Variant CJD in an individual heterozygous for PRNP codon 129

The Lancet (British edition), 2009-12, Vol.374 (9707), p.2128-2128

2009

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Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Human molecular genetics, 2012-04, Vol.21 (8), p.1897-1906

2012

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Behavioral and Psychiatric Symptoms in Prion Disease

The American journal of psychiatry, 2014-03, Vol.171 (3), p.265-274

2014

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In vitro screen of prion disease susceptibility genes using the scrapie cell assay

Human molecular genetics, 2014-10, Vol.23 (19), p.5102-5108

2014

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

Alzheimer's & dementia : diagnosis, assessment & disease monitoring, 2019-12, Vol.11 (1), p.277-280

2019

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PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit

Human mutation, 2010-07, Vol.31 (7), p.E1551-E1563

2010

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Familial Creutzfeldt-Jakob disease in an Indian kindred

Annals of the Indian Academy of Neurology, 2019-10, Vol.22 (4), p.458-461

2019

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The clinical, neuroanatomical, and neuropathologic phenotype of TBK1 -associated frontotemporal dementia: A longitudinal case report

Alzheimer's & dementia : diagnosis, assessment & disease monitoring, 2017, Vol.6 (1), p.75-81

2017

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Genome wide association studies and prion disease

Prion, 2011-07, Vol.5 (3), p.154-160

2011

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Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery

Acta neuropathologica, 2018-05, Vol.135 (5), p.671-679

2018

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Academic neurology in the UK: a plea to turn away from the precipice

Brain (London, England : 1878), 2024-05, Vol.147 (7), p.2270-2273

2024

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Review: An update on clinical, genetic and pathological aspects of frontotemporal lobar degenerations

Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes

Review: Fluid biomarkers in the human prion diseases

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

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura

A naturally occurring variant of the human prion protein completely prevents prion disease

Age at onset in genetic prion disease and the design of preventive clinical trials

The Intractable Puzzle of Sporadic Creutzfeldt-Jakob Disease in Very Young People

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine

Prion protein gene M232R variation is probably an uncommon polymorphism rather than a pathogenic mutation

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

The Medical Research Council Prion Disease Rating Scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies

Variant CJD in an individual heterozygous for PRNP codon 129

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Behavioral and Psychiatric Symptoms in Prion Disease

In vitro screen of prion disease susceptibility genes using the scrapie cell assay

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

PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit

Familial Creutzfeldt-Jakob disease in an Indian kindred

The clinical, neuroanatomical, and neuropathologic phenotype of TBK1 -associated frontotemporal dementia: A longitudinal case report

Genome wide association studies and prion disease

Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgery

Academic neurology in the UK: a plea to turn away from the precipice

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