Results 11 to 20 of about 50,646 (233)
Detecting frontotemporal dementia syndromes using MRI biomarkers
Background: Diagnosing frontotemporal dementia may be challenging. New methods for analysis of regional brain atrophy patterns on magnetic resonance imaging (MRI) could add to the diagnostic assessment.
Marie Bruun +16 more
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A frontotemporal dementia-like case after high-altitude climbing
Background We report a case who developed long-term neuropsychiatric sequelae similar to frontotemporal dementia after suffering a "high altitude sickness" while climbing a high mountain without taking precautions against acute hypoxia. Case presentation
Cemile Hazan Tunalı +2 more
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The behavioral variant of frontotemporal dementia is usually a sporadic and progressive neurodegenerative disorder. Here, we report the subacute onset of a frontotemporal dementia phenotype with a treatable etiology.
Kyan Younes +3 more
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Introduction Apraxia is common in neurodegenerative dementias but underrepresented in clinical workup for differential diagnoses. Methods Praxis‐profiles were assessed with the Dementia Apraxia Test in 93 patients with early stages of biologically ...
Andreas Johnen +4 more
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A case of familial frontotemporal dementia caused by a progranulin gene mutation
After Alzheimer’s disease, Frontotemporal dementia (FTD) is the most common cause of early-onset dementia. Several genetic mutations have been identified in familial FTD, with mutations in progranulin (GRN) accounting for approximately 20–25% of familial
Lauryn Currens +7 more
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Phenocopy syndrome of frontotemporal dementia
Introduction Frontotemporal dementia (FTD) is a group of neurodegenerative disorders characterized by behavioral or language changes with progressive executive dysfunction. It´s subdivided into two variants, the behavioral and language variants.
D. Martins +3 more
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Treatment of Frontotemporal Dementia [PDF]
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
The phenotypes of the behavioral variant of frontotemporal dementia and the corticobasal syndrome present considerable clinical and anatomical overlap.
Fernanda Tovar-Moll +7 more
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Frontotemporal Dementias [PDF]
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
Frontotemporal Dementia: A Clinical Review
Frontotemporal dementia is a disease in which atrophic changes occur in the frontal lobes and frontal temporal lobes of the brain. Frontotemporal dementias are a clinically, neuroanatomically and pathologically diverse group of diseases that ...
Michał Dacka +9 more
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