Frontotemporal dementia (FTD) is the second most common degenerative dementia after
Alzheimer's disease and its Lewy body variant. Clinical pathology can be subdivided in …

Hereditary frontotemporal dementia (FTD) is an autosomal dominant neurodegenerative
disorder that is associated with mutations in the tau gene and with the pathological …

Histological and immunohistochemical findings in 20 cases of frontotemporal dementias–8
cases of dementia of frontal lobe type (DFT), 7 cases of Pick's disease (PD), and 5 cases of …

A large Danish family has previously been reported in which autosomal dominant
frontotemporal dementia (FTD) is genetically linked to chromosome 3 (FTD-3). A mutation …

Ubiquitin-positive tau-negative inclusions were initially described in the rare form of
frontotemporal dementia (FTD) associated with motor neuron disease. However, recent …

Attempts at classification of fronto-temporal dementias have not yet been completely
successful. We report ten cases of sporadic fronto-temporal dementia (FTD) with ubiquitin …

Frontotemporal dementia (FTD) is an uncommon but important form of degenerative
disease. It may make up 50% of dementia cases presenting before age 60. The symptoms …

The most common histologic feature in patients with frontotemporal lobar degeneration
(FTLD) is intracellular brain inclusions of yet uncharacterized proteins that react with …

Objective: To describe the clinical features, neuropathology, and genetic studies in a family
with autosomal dominant frontotemporal dementia (FTD). Background: Clinical Pick's …

Background Frontotemporal lobar degeneration comprises a group of diseases with clinical
presentations and underlying histopathologies that overlap. Familial disease occurs in up to …