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


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).

Publication DOI: https://doi.org/10.1111/j.1365-2990.2011.01188.x
Divisions: Life & Health Sciences > Ophthalmic Research Group
Life & Health Sciences > Vision, Hearing and Language
Life & Health Sciences
Life & Health Sciences > Optometry
Life & Health Sciences > Clinical and Systems Neuroscience
Additional Information: The definitive version is available at wileyonlinelibrary.com © Journal, the British Neuropathological Society and Blackwell Publishing
Uncontrolled Keywords: density,frontotemporal lobar degeneration with transactive response, DNA-binding protein of 43 kDa,proteinopathy,neuronal cytoplasmic inclusions,neuronal intranuclear inclusion,Clinical Neurology,Pathology and Forensic Medicine,Neurology,Histology,Physiology (medical)
Full Text Link: http://onlineli ... 1188.x/abstract
Related URLs: http://www.scop ... tnerID=8YFLogxK (Scopus URL)
PURE Output Type: Article
Published Date: 2012-02
Published Online Date: 2012-01-06
Authors: Armstrong, Richard A. ( 0000-0002-5046-3199)
Carter, D.
Cairns, N.J.



Version: Accepted Version

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