Results 11 to 20 of about 24,976 (233)

Frontotemporal Lobar Degeneration and microRNAs [PDF]

Frontiers in Aging Neuroscience, 2016
Frontotemporal lobar degeneration (FTLD) includes a spectrum of disorders characterized by changes of personality and social behaviour and, often, a gradual and progressive language dysfunction.
Paola ePiscopo, DIEGO eALBANI, Anna Elisa eCastellano, Gianluigi eForloni, Annamaria eConfaloni   +4 more
doaj   +3 more sources

Delusions in frontotemporal lobar degeneration [PDF]

Journal of Neurology, 2009
We assessed the significance and nature of delusions in frontotemporal lobar degeneration (FTLD), an important cause of young-onset dementia with prominent neuropsychiatric features that remain incompletely characterised.
Alladi, Arciniegas, Bak, Ballard, Cairns, Catherine J. Mummery, Chan, Clement T. Loy, Elizabeth L. Sampson, Engelborghs, Geroldi, Gregory, Gregory, Hirono, Hodges, Howard, Jason D. Warren, Levy, Martin N. Rossor, McKhann, Mendez, Mendez, Neary, Nick C. Fox, Nitrini, Ogar, Rascovsky, Rohani Omar, Rosen, Scarmeas, Swartz, Tartaglia, Waddington   +32 more
core   +6 more sources

HnRNP Pathologies in Frontotemporal Lobar Degeneration

Cells, 2023
Frontotemporal dementia (FTD) is the second most common form of young-onset (
Xinwa Jiang, Ariana Gatt, Tammaryn Lashley   +2 more
doaj   +4 more sources

Frontotemporal lobar degeneration

Nature Reviews Disease Primers, 2023
Frontotemporal lobar degeneration (FTLD) is one of the most common causes of early-onset dementia and presents with early social-emotional-behavioural and/or language changes that can be accompanied by a pyramidal or extrapyramidal motor disorder. About 20-25% of individuals with FTLD are estimated to carry a mutation associated with a specific FTLD ...
Qutaiba Mahmoud
  +11 more sources

Genetics of frontotemporal lobar degeneration

Annals of Indian Academy of Neurology, 2010
Frontotemporal lobar degeneration (FTLD) is a highly heterogenous group of progressive neurodegenerative disorders characterized by atrophy of prefrontal and anterior temporal cortices.
Aswathy P, Jairani P, Mathuranath P
doaj   +3 more sources

Unpicking frontotemporal lobar degeneration [PDF]

Brain, 2011
Not so long ago, frontotemporal lobar degeneration (FTLD) seemed quite simple. Apart from rare variants of Alzheimer's disease and the occasional obscure neurodegenerative disease that could not be classified, FTLD was synonymous with Pick's disease, first described by Arnold Pick (1892) in a series of patients with ‘circumscribed atrophy’ and aphasia.
Love, Seth, Spillantini, Maria Grazia
openaire   +3 more sources

Frontotemporal Lobar Degeneration Without Lobar Atrophy [PDF]

Archives of Neurology, 2006
Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal inclusions (FTLD-U) is the most common form of frontotemporal dementia. Neuronal loss and gliosis in cornu ammonis 1 and the subiculum of the hippocampus are features of hippocampal sclerosis (HpScl), which occurs in many cases of FTLD-U.To determine if there were any ...
Keith A, Josephs, Jennifer L, Whitwell, Clifford R, Jack, Joseph E, Parisi, Dennis W, Dickson   +4 more
openaire   +2 more sources

Syndromes associated with frontotemporal lobar degeneration change response patterns on visual analogue scales

Scientific Reports, 2023
Self-report scales are widely used in cognitive neuroscience and psychology. However, they rest on the central assumption that respondents engage meaningfully.
Rebecca S. Williams, Natalie E. Adams, Laura E. Hughes, Matthew A. Rouse, Alexander G. Murley, Michelle Naessens, Duncan Street, Negin Holland, James B. Rowe   +8 more
doaj   +1 more source

Distinctive autophagy/mitophagy biomarker profiles in frontotemporal lobar degeneration and Alzheimer's disease. [PDF]

Acta Neuropathol Commun
Veverová K, Katonová A, Horáková H, Laczó J, Angelucci F, Hort J, Lautrup S, Fang EF, Vyhnálek M.   +8 more
europepmc   +3 more sources

WDR49-Positive Astrocytes Mark Severity of Neurodegeneration in Frontotemporal Lobar Degeneration and Alzheimer's Disease. [PDF]

Glia
Rajicic A, Giannini LAA, Gerrits E, van Buuren R, Melhem S, Slotman JA, Rozemuller AJM, Eggen BJL, van Swieten JC, Seelaar H.   +9 more
europepmc   +3 more sources