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Photograph: Allstar People with FTD end up in prison in this way.
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FTD-iPSCs were fated to cortical neurons, the cells most affected in FTD.
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Frontal variant FTD is an unpredictable disease in terms of its biochemistry.
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Methods: Sixty-two patients with a clinical diagnosis of FTD participated in the study.
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Loss of language nevertheless remains the most noticeable symptom of FTD.
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Methods: Electronic databases were searched using terms related to frontotemporallobardegeneration and movement disorders.
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Mutations in the gene encoding PGRN give rise to shortage of PGRN and cause familial frontotemporallobardegeneration.
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Summary: This represents the first systematic review and meta-analysis of the occurrence of movement disorder phenomenology in genetic frontotemporallobardegeneration.
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These findings further highlight that plasma PGRN levels may not accurately predict clinical features or response to future frontotemporallobardegeneration therapies.
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Mutations in various RBPs cause several diseases of the central nervous system, including frontotemporallobardegeneration, amyotrophic lateral sclerosis and fragile X syndrome.
Usage of frontotemporal dementia in English
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Recent research on frontotemporaldementia highlights the potential value of these approaches.
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Results: The frontotemporaldementia subgroup represented approximately half of all FTLD diagnoses.
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Other diseases which may involve tau deposition include frontotemporaldementia and corticobasal degeneration.
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Neuroimaging features were consistent with the diagnosis of frontotemporaldementia.
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The authors conclude that PSEN1 mutations can be associated with clinical features of frontotemporaldementia.
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Objective: We studied the clinical value of the faux pas test to diagnose behavioral-variant frontotemporaldementia.
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Conclusions: Our results confirm that the FPT capture's specific cognitive impairments in patients with behavioral-variant frontotemporaldementia.
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Our findings suggest that interleukin-15 may be implicated in the pathophysiology of Alzheimer's disease and frontotemporaldementia.
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To date, no longitudinal neuroimaging study has tested this hypothesis in vivo in frontotemporaldementia spectrum disorders.
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These expansions are also a frequent cause of frontotemporaldementia, emphasizing the molecular overlap between ALS and FTD.
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Objective: To correlate baseline resting-state measures within the salience network and changes in behavior among patients with frontotemporaldementia.
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A spokesman for the Welsh-born comedian said: Terry has been diagnosed with primary progressive aphasia, a variant of frontotemporaldementia.
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It has also been associated with increased white matter changes in frontotemporaldementia and risk of cognitive impairment in ALS.
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Psychiatric phenomena also define phenotypes such as frontotemporaldementia and dementia with Lewy bodies, cause distress, and amplify dementia-related disabilities.
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Causes of dementia include Alzheimer's disease, cerebrovascular disease, and lesser known entities such as frontotemporaldementia or dementia with Lewy bodies.
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Presenting signs were consistent with the behavioural variant of frontotemporaldementia in 17 of 21 patients.