We report a case of frontotemporal dementia caused by a novel MAPT mutation (Q351R) with a remarkably long amnestic presentation mimicking familial Alzheimer’s disease. Longitudinal clinical, neuropsychological and imaging data provide convergent evidence for predominantly bilateral anterior medial temporal lobe involvement consistent with previously established neuroanatomical signatures of MAPT mutations. This case supports the notion that the neural network affected in MAPT mutations is determined to a large extent by the underlying molecular pathology. We discuss the diagnostic significance of anomia in the context of atypical amnesia and the impact of impaired episodic and semantic memory systems on autobiographical memory
Familial Alzheimer’s disease (FAD) is considered a pathological model for sporadic Alzheimer’s dise...
The recently discovered hexanucleotide repeat expansion, C9ORF72, has been shown to be among the mos...
SummaryBackgroundFrontotemporal dementia is a highly heritable neurodegenerative disorder. In about ...
We report a case of frontotemporal dementia caused by a novel MAPT mutation (Q351R) with a remarkabl...
BACKGROUND AND OBJECTIVE: Mutations in the MAPT gene cause frontotemporal dementia (FTD). Most previ...
BACKGROUND AND OBJECTIVE: Mutations in the MAPT gene cause frontotemporal dementia (FTD). Most previ...
INTRODUCTION: A third of frontotemporal dementia (FTD) is caused by an autosomal-dominant genetic ...
Background and Objective: Mutations in the MAPT gene cause frontotemporal dementia (FTD). Most previ...
We have previously reported the initial clinical and imaging findings of a woman with a novel MAPT Q...
Background: The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotemporal de...
Background: The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotemporal...
Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American A...
Although executive dysfunction is the characteristic cognitive marker of behavioral variant frontote...
BACKGROUND: Frontotemporal dementia is a highly heritable neurodegenerative disorder. In about a thi...
Abstract Background The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotem...
Familial Alzheimer’s disease (FAD) is considered a pathological model for sporadic Alzheimer’s dise...
The recently discovered hexanucleotide repeat expansion, C9ORF72, has been shown to be among the mos...
SummaryBackgroundFrontotemporal dementia is a highly heritable neurodegenerative disorder. In about ...
We report a case of frontotemporal dementia caused by a novel MAPT mutation (Q351R) with a remarkabl...
BACKGROUND AND OBJECTIVE: Mutations in the MAPT gene cause frontotemporal dementia (FTD). Most previ...
BACKGROUND AND OBJECTIVE: Mutations in the MAPT gene cause frontotemporal dementia (FTD). Most previ...
INTRODUCTION: A third of frontotemporal dementia (FTD) is caused by an autosomal-dominant genetic ...
Background and Objective: Mutations in the MAPT gene cause frontotemporal dementia (FTD). Most previ...
We have previously reported the initial clinical and imaging findings of a woman with a novel MAPT Q...
Background: The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotemporal de...
Background: The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotemporal...
Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American A...
Although executive dysfunction is the characteristic cognitive marker of behavioral variant frontote...
BACKGROUND: Frontotemporal dementia is a highly heritable neurodegenerative disorder. In about a thi...
Abstract Background The MAPT c.1216C > T (p.Arg406Trp; R406W) mutation is a known cause of frontotem...
Familial Alzheimer’s disease (FAD) is considered a pathological model for sporadic Alzheimer’s dise...
The recently discovered hexanucleotide repeat expansion, C9ORF72, has been shown to be among the mos...
SummaryBackgroundFrontotemporal dementia is a highly heritable neurodegenerative disorder. In about ...