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Magnetite pollution nanoparticles in the human brain

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (39), p.10797-10801

2016

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Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype

Brain pathology (Zurich, Switzerland), 2017-11, Vol.27 (6), p.723-736

2017

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Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau

Acta neuropathologica, 2016-02, Vol.131 (2), p.267-280

2016

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Classification and pathology of primary progressive aphasia

Neurology, 2013-11, Vol.81 (21), p.1832-1839

2013

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The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2478-2492

2011

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Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Acta neuropathologica, 2010-01, Vol.119 (1), p.1-4

2010

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Detection of elevated levels of soluble α-synuclein oligomers in post-mortem brain extracts from patients with dementia with Lewy bodies

Brain (London, England : 1878), 2009-04, Vol.132 (4), p.1093-1101

2009

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Increased TDP-43 protein in cerebrospinal fluid of patients with amyotrophic lateral sclerosis

Acta neuropathologica, 2009, Vol.117 (1), p.55-62

2009

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Examining the language and behavioural profile in FTD and ALS-FTD

Journal of neurology, neurosurgery and psychiatry, 2017-08, Vol.88 (8), p.675-680

2017

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Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

Acta neuropathologica, 2009-01, Vol.117 (1), p.15-18

2009

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Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

Acta neuropathologica communications, 2013-10, Vol.1 (1), p.68-68, Article 68

2013

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Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

Neurology, 2013-05, Vol.80 (20), p.1881-1887

2013

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Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects

Acta neuropathologica, 2012-09, Vol.124 (3), p.373-382

2012

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Molecular analysis and biochemical classification of TDP-43 proteinopathy

Brain (London, England : 1878), 2012-11, Vol.135 (Pt 11), p.3380-3391

2012

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TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

Acta neuropathologica, 2011-12, Vol.122 (6), p.703-713

2011

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Pathological assessments for the presence of hexanucleotide repeat expansions in C9ORF72 in Alzheimer's disease

Acta neuropathologica communications, 2013-08, Vol.1 (1), p.50-50, Article 50

2013

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Histone deacetylase class II and acetylated core histone immunohistochemistry in human brains with Huntington’s disease

Brain research, 2013-04, Vol.1504, p.16-24

2013

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Cognitive–behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia

Journal of neurology, 2015-04, Vol.262 (4), p.916-922

2015

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TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration

Acta neuropathologica, 2008-08, Vol.116 (2), p.141-146

2008

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Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

Brain (London, England : 1878), 2008-03, Vol.131 (3), p.721-731

2008

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The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

Acta neuropathologica, 2011-07, Vol.122 (1), p.99-110

2011

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Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene

Neuropathology and applied neurobiology, 2015-08, Vol.41 (5), p.601-612

2015

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Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy

Acta neuropathologica, 2010-07, Vol.120 (1), p.55-66

2010

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Pathological correlates of frontotemporal lobar degeneration in the elderly

Acta neuropathologica, 2011-03, Vol.121 (3), p.365-371

2011

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α‐Synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma

The FASEB journal, 2003-10, Vol.17 (13), p.1-16

2003

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Magnetite pollution nanoparticles in the human brain

Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype

Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau

Classification and pathology of primary progressive aphasia

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Detection of elevated levels of soluble α-synuclein oligomers in post-mortem brain extracts from patients with dementia with Lewy bodies

Increased TDP-43 protein in cerebrospinal fluid of patients with amyotrophic lateral sclerosis

Examining the language and behavioural profile in FTD and ALS-FTD

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects

Molecular analysis and biochemical classification of TDP-43 proteinopathy

TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

Pathological assessments for the presence of hexanucleotide repeat expansions in C9ORF72 in Alzheimer's disease

Histone deacetylase class II and acetylated core histone immunohistochemistry in human brains with Huntington’s disease

Cognitive–behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia

TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene

Phosphorylated TDP-43 pathology and hippocampal sclerosis in progressive supranuclear palsy

Pathological correlates of frontotemporal lobar degeneration in the elderly

α‐Synuclein implicated in Parkinson's disease is present in extracellular biological fluids, including human plasma

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