Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration (Q38391502)

2 September 2017

Clinicopathological and genetic correlates of frontotemporal lobar degeneration and corticobasal degeneration (English)

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frontotemporal lobar degeneration

2 September 2017

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corticobasal degeneration

inferred from title

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Mario Ezquerra

4

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José Luis Molinuevo

object named as

José Luis Molinuevo

7

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Eduardo Tolosa

5

object named as

Eduardo Tolosa

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2 September 2017

Albert Lladó

1

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2 September 2017

Raquel Sánchez-Valle

2

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2 September 2017

Maria Jesús Rey

3

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2 September 2017

Isidro Ferrer

6

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2 September 2017

Catalan collaborative Study Group for FTLD

8

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2 September 2017

25 March 2008

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2 September 2017

7

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inferred from page(s)

published in

Journal of Neurology

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2 September 2017

255

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2 September 2017

4

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2 September 2017

488-494

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https://scigraph.springernature.com/pub.10.1007/s00415-008-0565-8

2 September 2017

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cites work

alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease

1 reference

https://api.crossref.org/works/10.1007%2FS00415-008-0565-8

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-008-0565-8

The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-008-0565-8

Accuracy of the clinical diagnosis of corticobasal degeneration: a clinicopathologic study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-008-0565-8

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-008-0565-8

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

21 January 2018

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12 December 2020

Clinical and pathological characterization of progressive aphasia

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12 December 2020

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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12 December 2020

Association between the extended tau haplotype and frontotemporal dementia.

1 reference

12 December 2020

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

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12 December 2020

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

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12 December 2020

Clinicopathological correlates in frontotemporal dementia

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12 December 2020

The genetic and pathological classification of familial frontotemporal dementia.

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12 December 2020

Ubiquitin-negative mini-pick-like bodies in the dentate gyrus in p301l tauopathy

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12 December 2020

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

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12 December 2020

Frequency of tau mutations in familial and sporadic frontotemporal dementia and other tauopathies

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12 December 2020

Primary progressive aphasia as the initial manifestation of corticobasal degeneration and unusual tauopathies.

1 reference

12 December 2020

Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

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12 December 2020

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

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12 December 2020

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

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12 December 2020

A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.

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12 December 2020

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

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12 December 2020

Atypical progressive supranuclear palsy with corticospinal tract degeneration.

1 reference

12 December 2020

10.1007/S00415-008-0565-8

Identifiers

DOI

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Dimensions Publication ID

2 September 2017

1032769502

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Fatcat ID

release_q5bs3udaanfctln37zi67zece4

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Fatcat

https://api.fatcat.wiki/v0/release/q5bs3udaanfctln37zi67zece4

24 November 2022

mapped directly with Wikidata item

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