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
Robert Rusina, Gabor G Kovacs, Jindřich Fiala, Jakub Hort, Petr Ridzoň, Iva Holmerová, Thomas Ströbel, Radoslav MatějVolume:
11
Language:
english
DOI:
10.1186/1471-2377-11-50
Date:
December, 2011
File:
PDF, 4.33 MB
english, 2011