… characterize familial forms with unknown genetic defects. … the existence of autosomal dominant
forms with unknown genetic … We suggest that familial forms with unknown genetic defects …

… The term frontotemporal dementia ( FTD ) describes a clinically… clarifies the terminology of
frontotemporal dementia (FTD) and … This article is part of the Frontotemporal Dementia special …

… The familial form of frontotemporal lobar degenerations with an autosomal dominant mode
of transmission was observed by Torsten Sjögren [10]. The first insight into the molecular …

… associated with C9orf72 mutations, the most common genetic form of the disorder.
Furthermore, C9orf72 mutations have been associated with schizophrenia and bipolar disorder. …

… The stereotypic form of frontotemporal dementia occurs in association with marked striatal
changes and variable cortical involvement, often with the emphasis on temporal rather than …

Frontotemporal dementia (FTD) has undergone numerous changes in nomenclature and
categorization schemes since it was first described by Pick in 1892. Presently, FTD …

… Clinically, frontotemporal dementias characteristically strike … and genetically mediated forms
of frontotemporal dementia have … assessment of the frontotemporal dementias, motivated by …

Frontotemporal dementia (FTD) is a clinically and pathologically heterogeneous group of
non-Alzheimer dementias characterised collectively by relatively selective, progressive atrophy …

… , many patients with the frontal, or behavioural, form of FTD (fvFTD) present first to psychiatrists
and … Management in all forms of FTD is essentially symptomatic and ideally involves a …

… of microtubule-associated-protein-tau-based pathological features in some patients and
the discovery, in some familial cases, of mutations in the tau gene links FTD to other forms of …