Objective To report the clinical manifestation and genetic characteristics of a patient having
frontotemporal dementia (FTD) with abnormal behavior and unstable walking. Methods The …

Background: Amyotrophic lateral sclerosis/frontotemporal dementia (ALS/FTD) includes a
large spectrum of neurodegenerative disorders. Objective: To identify the relationship of …

The clinical spectrum of frontotemporal lobar degeneration (FTLD) is characterized by
personality changes, language impairment, and executive function deficits. About 40% of …

Background: Behavioral variant frontotemporal dementia (bvFTD) typically involves subtle
changes in personality that can delay a timely diagnosis. Objective: Here, we report the case …

Background Behavioral variant frontotemporal dementia (bvFTD) is a clinically
heterogeneous syndrome with high heredity. However, the frequencies of mutations …

Frontotemporal lobar degeneration (FTLD) refers to a clinically, pathologically, and
genetically heterogeneous group of dementias that arises from the degeneration of the …

Background Frontotemporal dementia (FTD) is the second most common cause of early‐
onset neurodegenerative dementia. Up to 40% of FTD cases are inherited. Mutations in …

Background Methods The GRN mutations, especially of the loss of function type, are
causative of frontotemporal dementia (FTD). However, several GRN variants can be found in …

Background: During the twentieth century, frontotemporal dementia (FTD) was often
misdiagnosed, confused with Alzheimer's disease or psychiatric disorders, jeopardizing care …

The spectrum of GRN frontotemporal dementia (GRN-FTD) includes the behavioral variant
(bvFTD), primary progressive aphasia (PPA; further subcategorized as progressive …