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The role of lysosomes and autophagosomes in frontotemporal lobar degeneration

Neuropathology and applied neurobiology, 2019-04, Vol.45 (3), p.244-261

2019

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Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3091-3102

2006

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The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3081-3090

2006

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Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins

Neuropathology and applied neurobiology, 2016-04, Vol.42 (3), p.242-254

2016

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Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

Neurology, 2001-06, Vol.56 (12), p.1702-1706

2001

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Review: Recent progress in frontotemporal lobar degeneration

Neuropathology and applied neurobiology, 2010-02, Vol.36 (1), p.4-16

Pickering-Brown, S. M.

2010

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Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene

Brain (London, England : 1878), 2004-06, Vol.127 (6), p.1415-1426

2004

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Inherited frontotemporal dementia in nine british families associated with intronic mutations in the tau gene

Brain (London, England : 1878), 2002-04, Vol.125 (Pt 4), p.732-751

2002

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The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein

Neuropathology and applied neurobiology, 2004-02, Vol.30 (1), p.1-18

2004

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Genetic associations between cathepsin D exon 2 C→T polymorphism and Alzheimer’s disease, and pathological correlations with genotype

Journal of neurology, neurosurgery and psychiatry, 2006-04, Vol.77 (4), p.515-517

2006

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Association between apolipoprotein E e4 allele and arteriosclerosis, cerebral amyloid angiopathy, and cerebral white matter damage in Alzheimer’s disease

Journal of neurology, neurosurgery and psychiatry, 2004-05, Vol.75 (5), p.696-699

2004

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A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer’s disease

Journal of neurology, neurosurgery and psychiatry, 2004-10, Vol.75 (10), p.1475-1477

2004

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The apolipoprotein E ε4 allele selectively increases the risk of frontotemporal lobar degeneration in males

Journal of neurology, neurosurgery and psychiatry, 2006-02, Vol.77 (2), p.154-158

2006

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Pathological relationships between microglial cell activity and tau and amyloid β protein in patients with Alzheimer's disease

Neuroscience letters, 2002-10, Vol.331 (3), p.171-174

2002

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Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia

Annals of neurology, 1999-08, Vol.46 (2), p.243-248

1999

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Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease

Neuropathology and applied neurobiology, 2006-08, Vol.32 (4), p.374-387

2006

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A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease

Neuroscience letters, 2004-01, Vol.354 (2), p.103-106

2004

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The angiotensin 1-converting enzyme insertion (I)/deletion (D) polymorphism does not influence the extent of amyloid or tau pathology in patients with sporadic Alzheimer's disease

Neuroscience letters, 2002-08, Vol.328 (3), p.314-318

2002

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Amyloid β protein deposition in patients with frontotemporal lobar degeneration: relationship to age and apolipoprotein E genotype

Neuroscience letters, 2001-05, Vol.304 (3), p.161-164

2001

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Molecular classification of the dementias

The Lancet (British edition), 2000-02, Vol.355 (9204), p.626-626

2000

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Debrisoquine hydroxylase gene polymorphism (CYP2D64) in dementia with Lewy bodies

Journal of neurology, neurosurgery and psychiatry, 2003-01, Vol.74 (1), p.135-136

2003

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Frontotemporal dementia and parkinsonism associated with the IVS1+1G→A mutation in progranulin: a clinicopathologic study

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3103-3114

2006

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Tau load is associated with apolipoprotein E genotype and the amount of amyloid β protein, Aβ40, in sporadic and familial Alzheimer's disease

Neuropathology and applied neurobiology, 2003-02, Vol.29 (1), p.35-44

2003

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Mutations in progranulin explain atypical phenotypes with variants in MAPT

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3124-3126

2006

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Amyloid Angiopathy and Variability in Amyloid β Deposition Is Determined by Mutation Position in Presenilin-1-Linked Alzheimer’s Disease

The American journal of pathology, 2001-06, Vol.158 (6), p.2165-2175

2001

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The role of lysosomes and autophagosomes in frontotemporal lobar degeneration

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

Review: Recent progress in frontotemporal lobar degeneration

Frontotemporal dementia with Pick‐type histology associated with Q336R mutation in the tau gene

Inherited frontotemporal dementia in nine british families associated with intronic mutations in the tau gene

The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein

Genetic associations between cathepsin D exon 2 C→T polymorphism and Alzheimer’s disease, and pathological correlations with genotype

Association between apolipoprotein E e4 allele and arteriosclerosis, cerebral amyloid angiopathy, and cerebral white matter damage in Alzheimer’s disease

A polymorphic variation in the interleukin 1A gene increases brain microglial cell activity in Alzheimer’s disease

The apolipoprotein E ε4 allele selectively increases the risk of frontotemporal lobar degeneration in males

Pathological relationships between microglial cell activity and tau and amyloid β protein in patients with Alzheimer's disease

Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease

A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease

The angiotensin 1-converting enzyme insertion (I)/deletion (D) polymorphism does not influence the extent of amyloid or tau pathology in patients with sporadic Alzheimer's disease

Amyloid β protein deposition in patients with frontotemporal lobar degeneration: relationship to age and apolipoprotein E genotype

Molecular classification of the dementias

Debrisoquine hydroxylase gene polymorphism (CYP2D64) in dementia with Lewy bodies

Frontotemporal dementia and parkinsonism associated with the IVS1+1G→A mutation in progranulin: a clinicopathologic study

Tau load is associated with apolipoprotein E genotype and the amount of amyloid β protein, Aβ40, in sporadic and familial Alzheimer's disease

Mutations in progranulin explain atypical phenotypes with variants in MAPT

Amyloid Angiopathy and Variability in Amyloid β Deposition Is Determined by Mutation Position in Presenilin-1-Linked Alzheimer’s Disease

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