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

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Authors

  • 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).

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  • A quantitative study of the neuropathology

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

    Accepted author manuscript, 307 KB, PDF-document

Details

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

Bibliographic 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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