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

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

Frontotemporal dementia (FTD) encompasses several clinical syndromes that involve a
progressive change in behavior and/or language; it is more common than Alzheimer's …

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 …

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

This article examines the evolution in understanding of frontotemporal dementia (FTD)
during the last four decades. A central theme is the recognition of heterogeneity. Originally …

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

The term frontotemporal dementia (FTD) describes a clinically, genetically and
pathologically diverse group of neurodegenerative disorders. Symptoms of FTD can present …

Work done over the past decade has led to a molecular understanding of frontotemporal
lobar degeneration (FTLD), a deadly disease that afflicts patients in mid‐life. It is a common …

Frontotemporal dementia (FTD) is a clinical syndrome with a heterogeneous molecular
basis. The past decade has seen the discovery of several new FTD‐causing genetic …