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. and Cairns, N.J. (2012). A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP). Neuropathology and Applied Neurobiology, 38 (1), pp. 25-38.

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).

Publication DOI:	https://doi.org/10.1111/j.1365-2990.2011.01188.x
Divisions:	Life & Health Sciences > Ophthalmic Research Group Life & Health Sciences Life & Health Sciences > Optometry
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://onlinelibrary.wiley.com/doi/10.1111/j.1365-2990.2011.01188.x/abstract
Related URLs:	http://www.scopus.com/inward/record.url?scp=84855509969&partnerID=8YFLogxK (Scopus URL)
Published Date:	2012-02
Authors:	Armstrong, Richard A. ( 0000-0002-5046-3199) Carter, D. Cairns, N.J.

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