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

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

Frontotemporal dementia (FTD) is the second commonest cause of young onset dementia.
Our understanding of FTD and its related syndromes has advanced significantly in recent …

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 dementia (FTD) is a neurodegenerative disorder characterized by
progressive changes in behavior, personality, and language with involvement of the frontal …

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

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

Frontotemporal dementia (FTD) was one of the lesser known dementias until the recent
advancements revealing its genetic and pathological foundation. This common …

Today, frontotemporal dementia (FTD) remains one of the most common forms of early-onset
dementia, that is, before the age of 65, thus posing several diagnostic challenges to …