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Frontotemporal dementia [PDF]

open access: yesBritish Journal of Psychiatry, 2002
BackgroundFrontotemporal dementia accounts for up to 20% of cases of dementia in the presenium, yet remains poorly recognised. Diagnostic criteria have been devised to aid clinical diagnosis.AimsTo provide an overview of clinical and pathological characteristics of frontotemporal dementia and its nosological status.MethodsThe review summarises ...
Snowden, Julie S.   +2 more
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Frontotemporal dementia [PDF]

open access: yesBMJ, 2013
Frontotemporal dementia (FTD) encompasses several clinical syndromes that involve a progressive change in behavior and/or language; it is more common than Alzheimer's disease in early-onset dementia under the age of 60 years. In the behavioral variant of FTD (bvFTD) patients have social and emotional changes with prominent disinhibition, apathy, lack ...
Warren, JD, Rohrer, JD, Rossor, MN
openaire   +7 more sources

Frontotemporal Dementia [PDF]

open access: yesNeurologic Clinics, 2017
Frontotemporal dementia (FTD) is a heterogeneous disorder with distinct clinical phenotypes associated with multiple neuropathologic entities. Presently, the term FTD encompasses clinical disorders that include changes in behavior, language, executive control, and often motor symptoms.
Olney, Nicholas T   +2 more
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Frontotemporal dementia [PDF]

open access: yesThe Lancet, 2015
Frontotemporal dementia is an umbrella clinical term that encompasses a group of neurodegenerative diseases characterised by progressive deficits in behaviour, executive function, or language. Frontotemporal dementia is a common type of dementia, particularly in patients younger than 65 years. The disease can mimic many psychiatric disorders because of
Bang, Jee   +2 more
openaire   +3 more sources

Frontotemporal Dementia [PDF]

open access: yesNeurologic Clinics, 2016
Frontotemporal dementia (FTD) is a not-uncommon explanation for progressive cognitive deficit in patients who often have a genetic susceptibility for such a neurodegenerative process. However, FTD does not seem to identify one particular pathogenetic mechanism but rather a spectrum of pathologies with particular predilection for the frontal and ...
Roger E, Kelley, Ramy, El-Khoury
openaire   +2 more sources

Frontotemporal Dementias: A Review [PDF]

open access: yesAnnals of General Psychiatry, 2007
Abstract Dementia is a clinical state characterized by loss of function in multiple cognitive domains. It is a costly disease in terms of both personal suffering and economic loss. Frontotemporal dementia (FTD) is the term now preferred over Picks disease to describe the spectrum of non-Alzheimers dementias characterized by focal atrophy of ...
Rehan Aziz   +3 more
openaire   +4 more sources

Frontotemporal Dementias [PDF]

open access: yesCONTINUUM: Lifelong Learning in Neurology, 2016
This article reviews the common behavioral and cognitive features of frontotemporal dementia (FTD) and related disorders as well as the distinguishing clinical, genetic, and pathologic features of the most common subtypes.Advances in clinical phenotyping, genetics, and biomarkers have enabled improved predictions of the specific underlying molecular ...
openaire   +2 more sources

Treatment of Frontotemporal Dementia [PDF]

open access: yesCurrent Treatment Options in Neurology, 2014
Frontotemporal dementia (FTD) encompasses a spectrum of neurodegenerative diseases with heterogeneous clinical presentations and two predominant types of underlying neuropathology. FTD typically comprises three distinct clinical syndromes: behavioral variant frontotemporal dementia (bvFTD), semantic variant primary progressive aphasia (svPPA), and ...
Tsai, Richard M, Boxer, Adam L
openaire   +4 more sources

Genetics of Frontotemporal Dementia [PDF]

open access: yesCurrent Neurology and Neuroscience Reports, 2016
Frontotemporal dementia (FTD) is the second most common cause of dementia following Alzheimer's disease (AD). Between 20 and 50% of cases are familial. Mutations in MAPT, GRN and C9orf72 are found in 60% of familial FTD cases. C9orf72 mutations are the most common and account for 25%. Rarer mutations (
Emer Fallon   +3 more
openaire   +6 more sources

Inheritance of Frontotemporal Dementia [PDF]

open access: yesArchives of Neurology, 1999
Previous studies of families with fronto-temporal dementia (FTD) support an autosomal dominant inheritance pattern, but most studies have described genetic transmission in individual families specifically selected for the presence of multiple affected individuals.To investigate the familial presentation and inheritance of FTD and related disorders ...
Tiffany W. Chow   +3 more
openaire   +3 more sources

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