(Q48342107)

10 February 2018

title

Mixed tau, TDP-43 and p62 pathology in FTLD associated with a C9ORF72 repeat expansion and p.Ala239Thr MAPT (tau) variant (English)

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10 February 2018

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3

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Bradley N. Smith

object named as

Bradley N Smith

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Maria Grazia Spillantini

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object named as

Maria Grazia Spillantini

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10 February 2018

author name string

Andrew King

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10 February 2018

Safa Al-Sarraj

2

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Satomi Maekawa

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Mariangela Iovino

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Christopher E Shaw

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10 February 2018

publication date

28 September 2012

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10 February 2018

published in

Acta Neuropathologica

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10 February 2018

volume

125

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10 February 2018

issue

2

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10 February 2018

page(s)

303-310

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10 February 2018

https://scigraph.springernature.com/pub.10.1007/s00401-012-1050-0

exact match

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cites work

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Frontotemporal lobar degeneration with ubiquitinated tau-negative inclusions and additional alpha-synuclein pathology but also unusual cerebellar ubiquitinated p62-positive, TDP-43-negative inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

A harmonized classification system for FTLD-TDP pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Mutations in progranulin explain atypical phenotypes with variants in MAPT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Frontotemporal dementia due to C9ORF72 mutations: clinical and imaging features

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

21 January 2018

1 reference

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Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

21 January 2018

1 reference

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Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

An MND/ALS phenotype associated with C9orf72 repeat expansion: abundant p62-positive, TDP-43-negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-012-1050-0

10.1007/S00401-012-1050-0

21 January 2018

Identifiers

DOI

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10 February 2018

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10 February 2018