Background: Frontotemporal dementia (FTD) describes a cluster of neurocognitive
syndromes that present with impairment of executive functioning, changes in behavior, and …

Frontotemporal dementia (FTD) is a heterogeneous clinical syndrome characterized by
frontotemporal lobar degeneration (FTLD). Neuropathologically, FTLD is characterized by …

Frontotemporal dementia (FTD) is an increasingly recognized cause of dementia. This
review discusses the different FTD clinical syndromes and frontotemporal lobar …

Frontotemporal lobar degeneration (FTLD) is a heterogeneous disease entity encompassing
a wide variety of histopathological features and genetic backgrounds. The last two decades …

Recent advances in the genetics of neurodegenerative diseases have substantially
improved our knowledge about the genetic causes of frontotemporal lobar degeneration …

Background Frontotemporal dementia is the second most common cause of presenile
dementia and is a clinically, genetically and pathologically heterogeneous syndrome. The …

The last decade marked a turning point in the knowledge of frontotemporal lobar
degenerations (FTLD). Major discoveries were made with the identification of TDP-43 and …

Frontotemporal dementia (FTD) encompasses a heterogeneous group of clinical syndromes
marked by progressive neurodegeneration in frontal and temporal brain regions. FTD …

In this review, the authors outline a clinical approach to frontotemporal lobar degeneration
(FTLD), a term coined to describe a pathology associated with atrophy of the frontal and …

Frontotemporal lobar degeneration (FTLD) comprises a heterogenous group of fatal
neurodegenerative diseases and, to date, no validated diagnostic or prognostic biomarkers …