Frontotemporal dementia (FTD) is the second most common young-onset dementia and is
clinically characterised by progressive behavioural change, executive dysfunction and …

The landscape of frontotemporal dementia (FTD) has evolved remarkably in recent years
and is barely recognizable from two decades ago. Knowledge of the clinical …

Frontotemporal dementias are a clinically, neuroanatomically, and pathologically diverse
group of diseases that collectively constitute an important cause of young-onset dementia …

Frontotemporal dementia (FTD) is a genetically and pathologically heterogeneous disorder
characterized by personality changes, language impairment, and deficits of executive …

Abstract Frontotemporal Lobar Degeneration (FTLD) is a clinically, pathologically and
genetically heterogeneous group of disorders that affect principally the frontal and temporal …

Abstract Purpose of Review: This article reviews the common behavioral and cognitive
features of frontotemporal dementia (FTD) and related disorders as well as the …

In the past century, particularly the last decade, there has been enormous progress in our
understanding of frontotemporal dementia, a non‐Alzheimer's type dementia. Large …

Frontotemporal dementia (FTD) is a clinical syndrome with a heterogeneous molecular
basis. Familial FTD has been linked to mutations in several genes, including those encoding …

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 clinical syndrome with a heterogeneous molecular
basis. The neuropathology associated with most FTD is characterized by abnormal cellular …