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

Research output: Contribution to journalArticle

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 languageEnglish
Pages (from-to)25-38
Number of pages14
JournalNeuropathology and Applied Neurobiology
Volume38
Issue number1
Early online date6 Jan 2012
DOIs
Publication statusPublished - Feb 2012

Fingerprint

TDP-43 Proteinopathies
Frontotemporal Lobar Degeneration
DNA-Binding Proteins
Neuropathology

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

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). / Armstrong, Richard A.; Carter, D.; Cairns, N.J.

In: Neuropathology and Applied Neurobiology, Vol. 38, No. 1, 02.2012, p. 25-38.

Research output: Contribution to journalArticle

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