FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

<p>Abstract</p> <p>Background</p> <p>Frontotemporal lobar degeneration with ubiquitin and TDP-43 positive neuronal inclusions represents a novel entity (FTLD-TDP) that may be associated with motor neuron disease (FTLD-MND); involvement of extrapyramidal and other system...

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Bibliographic Details
Main Authors: Holmerová Iva, Ridzoň Petr, Hort Jakub, Fiala Jindřich, Kovacs Gabor G, Rusina Robert, Ströbel Thomas, Matěj Radoslav
Format: Article
Language:English
Published: BMC 2011-05-01
Series:BMC Neurology
Online Access:http://www.biomedcentral.com/1471-2377/11/50

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http://www.biomedcentral.com/1471-2377/11/50

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