(Q28306543)

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Progranulin and frontotemporal lobar degeneration

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title

Progranulin and frontotemporal lobar degeneration (English)

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main subject

frontotemporal lobar degeneration

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author

Stuart Pickering-Brown

object named as

Stuart M Pickering-Brown

series ordinal

1

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language of work or name

English

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publication date

July 2007

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published in

Acta Neuropathologica

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volume

114

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issue

1

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page(s)

39-47

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exact match

https://scigraph.springernature.com/pub.10.1007/s00401-007-0241-6

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cites work

Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.

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reference URL

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21 January 2018

Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.

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reference URL

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21 January 2018

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

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reference URL

https://api.crossref.org/works/10.1007%2FS00401-007-0241-6

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21 January 2018

Cellular localization of gene expression for progranulin

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reference URL

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retrieved

21 January 2018

Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia

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21 January 2018

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

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21 January 2018

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

Tau gene mutation K257T causes a tauopathy similar to Pick's disease

1 reference

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reference URL

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21 January 2018

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

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Familial aggregation in frontotemporal dementia.

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reference URL

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retrieved

21 January 2018

Identifiers

DOI

10.1007/S00401-007-0241-6

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Dimensions Publication ID

1028822560

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PubMed ID

17572900

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(Q28306543)

Progranulin and frontotemporal lobar degeneration

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