Frontotemporal dementia (FTD) is a prevalent neurodegenerative disease of heterogeneous
histopathology. Neuropathological subtypes are identified on the basis of the presence or …

Frontotemporal dementia (FTD) is the second commonest young-onset neurodegenerative
dementia. The canonical clinical syndromes are a behavioural variant (bvFTD) and two …

In 2006, two papers were published, each describing pathological heterogeneity in cases of
frontotemporal lobar degeneration (FTLD) with ubiquitin-positive, tau-negative inclusions …

The objective of this article is to study the accuracy of antemortem clinical diagnoses of
frontotemporal lobar degenerations (FTLDs). From brain autopsies performed on subjects …

Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders
characterized by disturbances of behavior and personality and different types of language …

Frontotemporal dementia (FTD) comprises a group of behavioral, language, and movement
disorders. On the basis of the nature of the characteristic protein inclusions, frontotemporal …

Objective The pathology of frontotemporal dementia, termed frontotemporal lobar
degeneration (FTLD), is characterized by distinct molecular classes of aggregated proteins …

Frontotemporal lobar degeneration (FTLD) refers to a focal, non-Alzheimer form of cerebral
degeneration that encompasses the distinct clinical syndromes of frontotemporal dementia …

There is increasing recognition of a clinical overlap between frontotemporal dementia (FTD)
and amyotrophic lateral sclerosis (ALS). Recent advances in our understanding of the …

The pathological distinctions between the various clinical and pathological manifestations of
frontotemporal lobar degeneration (FTLD) remain unclear. Using monoclonal antibodies …