A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)

Richard A. Armstrong; D. Carter; N.J. Cairns

doi:10.1111/j.1365-2990.2011.01188.x

A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)

Richard A. Armstrong, D. Carter, N.J. Cairns

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Abstract

To further characterize the neuropathology of the heterogeneous molecular disorder frontotemporal lobar degeneration (FTLD) with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy (FTLD-TDP).

Original language	English
Pages (from-to)	25-38
Number of pages	14
Journal	Neuropathology and Applied Neurobiology
Volume	38
Issue number	1
Early online date	6 Jan 2012
DOIs	https://doi.org/10.1111/j.1365-2990.2011.01188.x
Publication status	Published - Feb 2012

Bibliographical note

The definitive version is available at wileyonlinelibrary.com
© Journal, the British Neuropathological Society and Blackwell Publishing

Keywords

density
frontotemporal lobar degeneration with transactive response
DNA-binding protein of 43 kDa
proteinopathy
neuronal cytoplasmic inclusions
neuronal intranuclear inclusion

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10.1111/j.1365-2990.2011.01188.x

A quantitative study of the neuropathology
The definitive version is available at wileyonlinelibrary.com © Journal, the British Neuropathological Society and Blackwell Publishing
Accepted author manuscript, 307 KB

http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2990.2011.01188.x/abstract

Cite this

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A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)

Abstract

Bibliographical note

Keywords

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