The neurophysiological effect of NMDA-R antagonism of frontotemporal lobar degeneration is conditional on individual GABA concentration [PDF]
There is a pressing need to accelerate therapeutic strategies against the syndromes caused by frontotemporal lobar degeneration, including symptomatic treatments.
Alistair Perry +10 more
doaj +2 more sources
There is extensive synaptic loss from frontotemporal lobar degeneration, in preclinical models and human in vivo and post mortem studies. Understanding the consequences of synaptic loss for network function is important to support translational models ...
David J. Whiteside +16 more
doaj +2 more sources
Signature laminar distributions of pathology in frontotemporal lobar degeneration [PDF]
Frontotemporal lobar degeneration (FTLD) with either tau (FTLD-tau) or TDP-43 (FTLD-TDP) inclusions are distinct proteinopathies that frequently cause similar frontotemporal dementia (FTD) clinical syndromes.
Daniel T. Ohm +15 more
openalex +2 more sources
Incidence of Syndromes Associated With Frontotemporal Lobar Degeneration in 9 European Countries [PDF]
This cohort study analyzes age- and sex-specific incidence rates of frontotemporal lobar degeneration–related disorders by phenotype across 9 European countries.
Giancarlo Logroscino +54 more
openalex +2 more sources
Clinical and Imaging Features of Sporadic and Genetic Frontotemporal Lobar Degeneration TDP‐43 A and B [PDF]
Objective Certain frontotemporal lobar degeneration subtypes, including TDP‐A and B, can either occur sporadically or in association with specific genetic mutations.
Sean Coulborn +17 more
doaj +2 more sources
Neuropathology of frontotemporal lobar degeneration: A review [PDF]
Frontotemporal lobar degeneration (FTLD) is the second most common cause of presenile dementia. Three main clinical variants are widely recognized within the FTLD spectrum: the behavioural variant of frontotemporal dementia (bvFTD), semantic dementia (SD)
Valéria Santoro Bahia +2 more
doaj +2 more sources
BackgroundMutations in granulin (PGRN) and tau (MAPT), and hexanucleotide repeat expansions near the C9orf72 genes are the most prevalent genetic causes of frontotemporal lobar degeneration.
Carmen Gasca-Salas +6 more
doaj +3 more sources
Longitudinal grey and white matter changes in frontotemporal dementia and Alzheimer's disease [PDF]
Behavioural variant frontotemporal dementia (bvFTD) and Alzheimer's disease (AD) dementia are characterised by progressive brain atrophy. Longitudinal MRI volumetry may help to characterise ongoing structural degeneration and support the differential ...
AF Fotenos +50 more
core +13 more sources
Frontotemporal lobar degeneration
This PrimeView highlights the mechanisms, diagnosis, epidemiology and management of frontotemporal lobar degeneration.
M. Grossman +11 more
semanticscholar +2 more sources
Response to: Clinical Imaging Features of Sporadic and Genetic Frontotemporal Lobar Degeneration TDP‐43 A and B [PDF]
Sergi Borrego‐Écija +3 more
doaj +2 more sources

