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Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2565-2581

2011

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Testing an aetiological model of visual hallucinations in Parkinson's disease

Brain (London, England : 1878), 2011-11, Vol.134 (11), p.3299-3309

2011

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Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.736-750

2012

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Characterization of tau positron emission tomography tracer [18 F]AV-1451 binding to postmortem tissue in Alzheimer's disease, primary tauopathies, and other dementias

Alzheimer's & dementia, 2016-11, Vol.12 (11), p.1116-1124

2016

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Second consensus statement on the diagnosis of multiple system atrophy

Neurology, 2008-08, Vol.71 (9), p.670

2008

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A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

The New England journal of medicine, 2013-11, Vol.369 (20), p.1904-1914

2013

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A common LRRK2 mutation in idiopathic Parkinson's disease

The Lancet (British edition), 2005-01, Vol.365 (9457), p.415-416

2005

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Clinical, pathological and functional characterization of riboflavin-responsive neuropathy

Brain (London, England : 1878), 2017-11, Vol.140 (11), p.2820-2837

2017

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Apomorphine: A potential modifier of amyloid deposition in Parkinson's disease?

Movement disorders, 2016-05, Vol.31 (5), p.668-675

2016

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Mixed pathologies including chronic traumatic encephalopathy account for dementia in retired association football (soccer) players

Acta neuropathologica, 2017-03, Vol.133 (3), p.337-352

2017

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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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A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2548-2564

2011

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

Brain (London, England : 1878), 2005-12, Vol.128 (12), p.2786-2796

2005

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A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

Brain (London, England : 1878), 2008-03, Vol.131 (3), p.706-720

2008

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TREM2 Variants in Alzheimer's Disease

The New England journal of medicine, 2013-01, Vol.368 (2), p.117-127

2013

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A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia

Neuropathology and applied neurobiology, 2014-06, Vol.40 (4), p.502-513

2014

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Brain biopsy in dementia

Brain (London, England : 1878), 2005-09, Vol.128 (9), p.2016-2025

2005

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Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress

Journal of neurochemistry, 2006-07, Vol.98 (1), p.156-169

2006

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Rosai-Dorfman disease presenting with widespread intracranial and spinal cord involvement

Neurology, 2006-11, Vol.67 (9), p.1551

2006

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Prion-like α-synuclein pathology in the brain of infants with Krabbe disease

Brain (London, England : 1878), 2022-05, Vol.145 (4), p.1257-1263

2022

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Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium

Journal of Neural Transmission, 2015-07, Vol.122 (7), p.957-972

2015

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The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features

Neurobiology of aging, 2012-09, Vol.33 (9), p.2231.e7-2231.e14

2012

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An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies

Acta neuropathologica, 2006-04, Vol.111 (4), p.329-340

2006

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The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease

Acta neuropathologica communications, 2013-07, Vol.1 (1), p.31-31, Article 31

2013

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Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

Testing an aetiological model of visual hallucinations in Parkinson's disease

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Characterization of tau positron emission tomography tracer [18 F]AV-1451 binding to postmortem tissue in Alzheimer's disease, primary tauopathies, and other dementias

Second consensus statement on the diagnosis of multiple system atrophy

A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

A common LRRK2 mutation in idiopathic Parkinson's disease

Clinical, pathological and functional characterization of riboflavin-responsive neuropathy

Apomorphine: A potential modifier of amyloid deposition in Parkinson's disease?

Mixed pathologies including chronic traumatic encephalopathy account for dementia in retired association football (soccer) players

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

TREM2 Variants in Alzheimer's Disease

A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia

Assessment of β-amyloid deposits in human brain: a study of the BrainNet Europe Consortium

Brain biopsy in dementia

Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress

Rosai-Dorfman disease presenting with widespread intracranial and spinal cord involvement

Prion-like α-synuclein pathology in the brain of infants with Krabbe disease

Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium

The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features

An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer's disease

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