Pathologic diagnoses in frontotemporal lobar degeneration (FTLD) include tau-positive
FTLD and tau-negative FTLD. Two variants of tau-negative FTLD are FTLD with motor …

Background: Frontotemporal lobar degeneration (FTLD) is a clinically, genetically, and
pathologically heterogeneous neurodegenerative disorder. Two subtypes commonly …

The term frontotemporal lobar degeneration (FTLD) refers to a group of progressive brain
diseases, which preferentially involve the frontal and temporal lobes. Depending on the …

A clinically and pathologically heterogeneous type of frontotemporal lobar degeneration has
abnormal tau pathology in neurons and glia (FTLD-tau). Familial FTLD-tau is usually due to …

Objective: To assess the ability of the current diagnostic criteria for frontotemporal lobar
degeneration (FTLD) to differentiate FTLD from AD. Methods: Thirty cases with autopsy …

Frontotemporal lobar degeneration (FTLD) comprises two main classes of
neurodegenerative diseases characterized by neuronal/glial proteinaceous inclusions (ie …

Frontotemporal dementias are neurodegenerative diseases in which symptoms of frontal
and/or temporal lobe disease are the first signs of the illness, and as the diseases progress …

Frontotemporal lobar degeneration (FTLD) is generally recognised as a disorder with
presenile onset (that is before 65 years of age) with only occasional cases presenting later …

Background: Frontotemporal lobar degeneration (FTLD) is a common cause of non-
Alzheimer dementia, but its natural history and the factors related to mortality in affected …

We set out to determine the frequency of the different pathologies underlying frontotemporal
degeneration (FTD) in our brain bank series, by reviewing all cases of pathologically …