degeneration

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Related to Frontotemporal lobar degeneration: Frontotemporal dementia, frontal lobe dementia
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Sample autopsy signout for Example 4, hippocampal sclerosis and TAR DNA-binding protein 43 kDa (TDP-43) in late-onset frontotemporal lobar degeneration (FTLD).
Frontotemporal lobar degeneration is a brain disorder that typically leads to dementia and sometimes occurs in tandem with ALS.
The Stereotypy Rating Inventory for frontotemporal lobar degeneration.
Frontotemporal lobar degeneration is a diagnostic term that encompasses multiple distinct forms of this dementia syndrome, with the three major subtypes being frontotemporal dementia, semantic dementia, and primary progressive aphasia.
TDP-43: the relationship between protein aggregation and neurodegeneration in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.
Alzheimer's disease and frontotemporal lobar degeneration (FTLD) are two of the most prevalent forms of neurodegenerative disorders.
The study tested physicians' ability to distinguish between AD and frontotemporal lobar degeneration (FTLD), the third most common cause of degenerative dementia, using a three-dimensional imaging technique called fludeoxyglucose F18 (FDG-PET) scanning.
Victor Villemagne of the Austin Hospital, Melbourne, used florbetaben PET imaging in 26 Alzheimer's patients, 11 with frontotemporal lobar degeneration (FTLD), 6 with Lewy body dementia (LBD), and 26 healthy controls.