Imaging and fluid biomarkers in frontotemporal dementia
LH Meeter, LD Kaat, JD Rohrer… - Nature Reviews …, 2017 - nature.com
Frontotemporal dementia (FTD), the second most common type of presenile dementia, is a
heterogeneous neurodegenerative disease characterized by progressive behavioural …
heterogeneous neurodegenerative disease characterized by progressive behavioural …
Speech and language impairments in behavioral variant frontotemporal dementia: a systematic review
A Geraudie, P Battista, AM García, IE Allen… - Neuroscience & …, 2021 - Elsevier
Although behavioral variant frontotemporal dementia (bvFTD) is classically defined by
behavioral and socio-emotional changes, impairments often extend to other cognitive …
behavioral and socio-emotional changes, impairments often extend to other cognitive …
Distribution of dipeptide repeat proteins in cellular models and C9orf72 mutation cases suggests link to transcriptional silencing
MH Schludi, S May, FA Grässer, K Rentzsch… - Acta …, 2015 - Springer
A massive expansion of a GGGGCC repeat upstream of the C9orf72 coding region is the
most common known cause of amyotrophic lateral sclerosis and frontotemporal dementia …
most common known cause of amyotrophic lateral sclerosis and frontotemporal dementia …
Harmonization of brain diffusion MRI: concepts and methods
MS Pinto, R Paolella, T Billiet, P Van Dyck… - Frontiers in …, 2020 - frontiersin.org
MRI diffusion data suffers from significant inter-and intra-site variability, which hinders multi-
site and/or longitudinal diffusion studies. This variability may arise from a range of factors …
site and/or longitudinal diffusion studies. This variability may arise from a range of factors …
Genetics of frontotemporal dementia
DA Olszewska, R Lonergan, EM Fallon… - Current neurology and …, 2016 - Springer
Frontotemporal dementia (FTD) is the second most common cause of dementia following
Alzheimer's disease (AD). Between 20 and 50% of cases are familial. Mutations in MAPT …
Alzheimer's disease (AD). Between 20 and 50% of cases are familial. Mutations in MAPT …
[HTML][HTML] Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers
Hexanucleotide repeat expansions in C9ORF72 are the most common known genetic cause
of familial and sporadic frontotemporal dementia and amyotrophic lateral sclerosis. Previous …
of familial and sporadic frontotemporal dementia and amyotrophic lateral sclerosis. Previous …
Apathy and impulsivity in frontotemporal lobar degeneration syndromes
CJ Lansdall, ITS Coyle-Gilchrist, PS Jones… - Brain, 2017 - academic.oup.com
Apathy and impulsivity are common and disabling consequences of frontotemporal lobar
degeneration. They cause substantial carer distress, but their aetiology remains elusive …
degeneration. They cause substantial carer distress, but their aetiology remains elusive …
Diffusion magnetic resonance imaging-based biomarkers for neurodegenerative diseases
K Kamagata, C Andica, A Kato, Y Saito… - International Journal of …, 2021 - mdpi.com
There has been an increasing prevalence of neurodegenerative diseases with the rapid
increase in aging societies worldwide. Biomarkers that can be used to detect pathological …
increase in aging societies worldwide. Biomarkers that can be used to detect pathological …
Neuroimaging in dementia
AM Staffaroni, FM Elahi, D McDermott… - Seminars in …, 2017 - thieme-connect.com
Although the diagnosis of dementia still is primarily based on clinical criteria, neuroimaging
is playing an increasingly important role. This is in large part due to advances in techniques …
is playing an increasingly important role. This is in large part due to advances in techniques …
Neurofilament light chain as a biomarker, and correlation with magnetic resonance imaging in diagnosis of CNS-related disorders
The search for diagnostic and prognostic biomarkers for neurodegenerative conditions is of
high importance, since these disorders may present difficulties in differential diagnosis …
high importance, since these disorders may present difficulties in differential diagnosis …