A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP)-Reference-Cited by-同舟云学术

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

Published:2012-01-06 Issue:1 Volume:38 Page:25-38
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:

Author:

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

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2011.01188.x/fullpdf

Reference54 articles.

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4. Cortical ubiquitin positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study;Kovari;Acta Neuropathol,2004

5. TDP-43 familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions;Cairns;Am J Pathol,2007

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