Frontotemporal lobar degeneration (FTLD) represents a group of clinically,
neuropathologically and genetically heterogeneous disorders with plenty of overlaps …

The pattern and degree of brain atrophy in frontotemporal dementia (FTD) has the potential
for use as an aid in the diagnosis of this disorder and its differentiation from other …

Frontotemporal dementia is clinically and neuropathologically heterogeneous, but
neuroinflammation, atrophy and cognitive impairment occur in all of its principal syndromes …

Frontotemporal dementia (FTD) represents a spectrum of non-Alzheimer's degenerative
conditions associated with focal atrophy of the frontal and/or temporal lobes. Frontal and …

Objective: To compare patterns of brain atrophy in fronto-temporal dementia (FTD) and
Alzheimer's disease (AD) since atrophy in individual areas may not be sufficiently specific as …

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

OBJECTIVES The loss of the neurons in layer 3, one of the groups of cortical neurons most
vulnerable in various degenerative brain diseases, results in axonal degeneration leading to …

Few studies have assessed whether the patterns of neuropsychological impairment in
patients with different frontotemporal lobar degeneration (FTLD) subtypes remain distinct …

Progressive nonfluent aphasia (PNFA) is a clinical syndrome characterized by motor speech
impairment and agrammatism, with relative sparing of single word comprehension and …

Marked brain atrophy occurs in frontotemporal dementia (FTD) yet substantial variation
between cases is seen. Recently, a four-level staging scheme which reflects increasing …