Comparison of family histories in FTLD subtypes and related tauopathies

295Citations
Citations of this article
266Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Pedigrees from 269 patients with frontotemporal lobar degeneration (FTLD), including frontotemporal dementia (FTD), FTD with ALS (FTD/ ALS), progressive nonfluent aphasia, semantic dementia (SD), corticobasal degeneration, and progressive supranuclear palsy were analyzed to determine the degree of heritability of these disorders. FTD/ALS was the most and SD the least heritable subtype. FTLD syndromes appear to have different etiologies and recurrence risks. Copyright © 2005 by AAN Enterprises, Inc.

Cite

CITATION STYLE

APA

Goldman, J. S., Farmer, J. M., Wood, E. M., Johnson, J. K., Boxer, A., Neuhaus, J., … Miller, B. L. (2005). Comparison of family histories in FTLD subtypes and related tauopathies. Neurology, 65(11), 1817–1819. https://doi.org/10.1212/01.wnl.0000187068.92184.63

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free