Results 211 to 220 of about 24,976 (233)

DNA methylation as a contributor to dysregulation of STX6 and other frontotemporal lobar degeneration genetic risk-associated loci

Rambarack N, Fodder K, Murthy M, Toomey C, de Silva R, Humphrey J, Raj T, Lashley T, Bettencourt C.   +8 more
europepmc   +1 more source

Familial frontotemporal lobar degeneration

, 2015
openaire   +1 more source

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Frontotemporal Lobar Degeneration

CNS Drugs, 2012
Frontotemporal Lobar Degeneration (FTLD) is an heterogeneous neurodegenerative disorder characterized by behaviour and language disturbances, associated with degeneration of the frontal and temporal lobes. Three different clinical presentations have been described, namely behavioural variant Frontotemporal Dementia (bvFTD), Semantic Dementia (SD) and ...
Enrico, Premi, Alessandro, Padovani, Barbara, Borroni   +2 more
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Frontotemporal lobar degeneration

2015
Main imaging findings: Patterns of atrophy (CT/MRI) or functional alterations (PET/SPECT) supporting clinical diagnosis of FTLD variants: bvFTD: bilateral, often asymmetrical involvement of frontal and anterior temporal structures; nfvPPA: left posterior fronto-insular damage; svPPA: anterior temporal lobe involvement, usually left ...
Filippi M, Agosta F
openaire   +3 more sources

Imaging Frontotemporal Lobar Degeneration

Current Neurology and Neuroscience Reports, 2014
The term frontotemporal lobar degeneration (FTLD) refers to a group of neurodegenerative disorders that target the frontal and temporal lobes. It accounts for approximately 10 % of pathologically confirmed dementias but has been demonstrated to be as prevalent as Alzheimer's disease in patients below the age of 65.
Janine, Diehl-Schmid, Oezguer A, Onur, Jens, Kuhn, Traugott, Gruppe, Alexander, Drzezga   +4 more
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From frontotemporal lobar degeneration pathology to frontotemporal lobar degeneration biomarkers

International Review of Psychiatry, 2013
Frontotemporal dementia (FTD) is an increasingly recognized cause of dementia. This review discusses the different FTD clinical syndromes and frontotemporal lobar degeneration (FTLD) pathological correlates as well as new genetic and proteomic findings that have added to our understanding of FTLD pathogenesis.
Chadwick M, Hales, William T, Hu
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Frontotemporal Lobar Degeneration

Okayama Igakkai Zasshi (Journal of Okayama Medical Association)
Abstract Frontotemporal lobar degeneration (FTLD) refers to the diverse neuropathologies that are the primary causes of frontotemporal dementias (FTD). FTD refers to a spectrum of progressive dementia syndromes that can be broadly grouped into behavioral (behavioral variant FTD), language (primary progressive aphasias), and motor (FTD ...
Angelina J. Polsinelli, Dale Korinek, Elizabeth K. Vernon, Sophia Wang   +3 more
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Frontotemporal Lobar Degeneration

Gerontology, 2001
Frontotemporal lobar degeneration is the second most common form of cortical dementia in the presenium after Alzheimer’s disease. Clinically, based on consensus guidelines, three distinct disease entities can be distinguished: frontotemporal dementia, semantic dementia and progressive nonfluent aphasia. Dementia of frontal type and motor neuron disease
M. Tolnay, A. Probst
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Frontotemporal Lobar Degeneration

2017
Frontotemporal dementia (FTD) is an uncommon but important form of degenerative disease characterized by clinical syndromes that result from degeneration of the frontal and temporal lobes. FTD is divided based on clinical presentation into behavioral variant FTD (bvFTD), semantic dementia, and progressive nonfluent/agrammatic aphasia.
Jonathan Graff-Radford, Keith A. Josephs
openaire   +1 more source