Results 11 to 20 of about 364,393 (335)
Cerebrospinal fluid biomarkers predict frontotemporal dementia trajectory [PDF]
The prognostic value of cerebrospinal fluid neurofilament light chain, total tau, phosphorylated tau181, and amyloid beta1‐42 was examined in frontotemporal dementia subtypes.
et al,, Fagan, Anne M, Jerome, Gina
core +3 more sources
The tailored activity program (TAP) to address behavioral disturbances in frontotemporal dementia: a feasibility and pilot study [PDF]
Purpose: To explore the feasibility of implementing the Tailored Activity Program with a cohort of people with frontotemporal dementia and their carers (dyads).
Allen CK+17 more
core +2 more sources
Dissociating memory networks in early Alzheimer's disease and frontotemporal lobar degeneration - a combined study of hypometabolism and atrophy [PDF]
Introduction: We aimed at dissociating the neural correlates of memory disorders in Alzheimer’s disease (AD) and frontotemporal lobar degeneration (FTLD).
Barthel, Henryk+9 more
core +14 more sources
Recently, there has been a growing research interest in utilizing the electroencephalogram (EEG) as a non-invasive diagnostic tool for neurodegenerative diseases.
Andreas Miltiadous+10 more
semanticscholar +1 more source
Regional Glymphatic Abnormality in Behavioral Variant Frontotemporal Dementia
Glymphatic function has not yet been explored in behavioral variant frontotemporal dementia (bvFTD). The spatial correlation between regional glymphatic function and bvFTD remains unknown.
Deming Jiang+9 more
semanticscholar +1 more source
Objectives This longitudinal study compared emerging plasma biomarkers for neurodegenerative disease between controls, patients with Alzheimer’s disease (AD), Lewy body dementia (LBD), frontotemporal dementia (FTD) and progressive supranuclear palsy (PSP)
Leonidas Chouliaras+12 more
semanticscholar +1 more source
Clinical heterogeneity in a family with flail arm syndrome and review of hnRNPA1‐related spectrum
Abstract Objective Flail arm syndrome (FAS) is one of the atypical subtypes of amyotrophic lateral sclerosis (ALS). Mutations in hnRNPA1 encoding heterogeneous nuclear ribonucleoprotein (hnRNP) A1 are a rare genetic cause of ALS. Herein, marked clinical heterogeneity of FAS in a pedigree with a known hnRNPA1 variant was described to raise early ...
Xiaochen Han+5 more
wiley +1 more source
Biomarker discovery and development for frontotemporal dementia and amyotrophic lateral sclerosis
Frontotemporal dementia refers to a group of neurodegenerative disorders characterized by behaviour and language alterations and focal brain atrophy. Amyotrophic lateral sclerosis is a rapidly progressing neurodegenerative disease characterized by loss ...
J. S. Katzeff+10 more
semanticscholar +1 more source
Dementia is the clinical syndrome characterized by progressive loss of cognitive and emotional abilities to a degree severe enough to interfere with daily functioning. Alzheimer’s disease (AD) is the most common neurogenerative disorder, making up 50–70%
Andreas Miltiadous+6 more
semanticscholar +1 more source
SPEECH AND LANGUAGE ABILITIES OF PERSONS WITH FRONTOTEMPORAL DEMENTIA [PDF]
The review outlines the importance of understanding speech and language difficulties that occur among the first symptoms of frontotemporal dementia, as well as the role of speech therapists in the management of people with frontotemporal dementia ...
Banović, Silva, Sinanović, Osman
core +3 more sources