Results 151 to 160 of about 47,802 (187)
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Psychiatric Clinics of North America, 2015
Frontotemporal dementia (FTD) is a heterogeneous group of hereditary and sporadic neurodegenerative disorders affecting frontotemporal areas. FTD, a leading cause of young-onset dementia, is often initially mistaken for primary psychiatric disorders.
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Frontotemporal dementia (FTD) is a heterogeneous group of hereditary and sporadic neurodegenerative disorders affecting frontotemporal areas. FTD, a leading cause of young-onset dementia, is often initially mistaken for primary psychiatric disorders.
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Frontotemporal Dementia and Mania
American Journal of Psychiatry, 2007“Ms. V,” a 60-year-old college-educated woman, was brought by her daughter to the emergency department at a teaching hospital for the evaluation of heart palpitations. Ms. V had personality changes and mood swings with aggressive verbal and physical behaviors that had progressively worsened over the past year.
Joshua D, Woolley +5 more
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Neuroimaging in frontotemporal dementia
International Review of Psychiatry, 2013The term frontotemporal dementia (FTD) refers to a group of neurodegenerative disorders that are associated with atrophy of the frontal and temporal lobes, and present clinically with impairments of behaviour or language. Three main subtypes are described, behavioural variant FTD (bvFTD) and two subtypes of the language presentation (known as primary ...
Jonathan D, Rohrer, Howard J, Rosen
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Continuum
This article discusses frontotemporal dementia (FTD) syndromes using a simplified framework of three core syndromes, including details on their pathology and unique genetic variations.FTD includes at least seven major clinical syndromes. The three core syndromes are behavioral variant FTD and two forms of progressive aphasia, commonly referred to as ...
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This article discusses frontotemporal dementia (FTD) syndromes using a simplified framework of three core syndromes, including details on their pathology and unique genetic variations.FTD includes at least seven major clinical syndromes. The three core syndromes are behavioral variant FTD and two forms of progressive aphasia, commonly referred to as ...
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Neuroinflammation in frontotemporal dementia
Nature Reviews Neurology, 2019Frontotemporal dementia (FTD) refers to a group of progressive neurodegenerative disorders with different pathological signatures, genetic variability and complex disease mechanisms, for which no effective treatments exist. Despite advances in understanding the underlying pathology of FTD, sensitive and specific fluid biomarkers for this disease are ...
Fiona Bright +10 more
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Survival in frontotemporal dementia
Neurology, 2003To establish survival in patients with pathologically confirmed frontotemporal dementia (FTD) and to determine whether clinical or pathologic subtype affects prognosis.The authors reviewed the presenting clinical features of 61 patients with dementia and pathologically confirmed FTD studied in Sydney (n = 31) and Cambridge (n = 30) over a 10-year ...
J R, Hodges +4 more
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The genetics of frontotemporal dementia
2008Publisher Summary This chapter emphasizes that frontotemporal dementia (FTD) is the second most common form of primary degenerative dementia after Alzheimer's disease (AD). The onset of the disease is most commonly in middle age between 45 and 65 years.
Pickering-Brown, Stuart, Hutton, Michael
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Psychosis in Frontotemporal Dementia
Journal of Alzheimer's Disease, 2014Frontotemporal dementia (FTD) is a neurodegenerative disorder, associated with a progressive decline in behavior caused by focal degeneration of the frontal lobes. Psychosis was an underestimated symptom of FTD, however, recent genetic research has revealed a high prevalence of psychosis in certain genetic groups.
Shunichiro, Shinagawa +6 more
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Depression in Frontotemporal Dementia
Psychosomatics, 2009The authors describe mood abnormalities seen in a case series of patients with frontotemporal dementia (FTD).Authors provide a structured review of outpatient and inpatient charts of FTD patients.Three distinct depressive syndromes were identified: The first corresponds to DSM-IV major depression.
David M, Blass, Peter V, Rabins
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