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 …
The genetics and neuropathology of frontotemporal lobar degeneration
A Sieben, T Van Langenhove, S Engelborghs… - Acta …, 2012 - Springer
Frontotemporal lobar degeneration (FTLD) is a heterogeneous group of disorders
characterized by disturbances of behavior and personality and different types of language …
characterized by disturbances of behavior and personality and different types of language …
Portuguese family with the co-occurrence of frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis phenotypes due to progranulin gene mutation
MR Almeida, MC Macário, L Ramos, I Baldeiras… - Neurobiology of …, 2016 - Elsevier
We and others have reported heterozygous progranulin mutations as an important cause of
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …
frontotemporal lobar degeneration (FTLD). It has been identified a complete progranulin …
Psychiatric symptoms in frontotemporal dementia: epidemiology, phenotypes, and differential diagnosis
D Galimberti, B Dell'Osso, AC Altamura, E Scarpini - Biological Psychiatry, 2015 - Elsevier
Frontotemporal dementia (FTD) is the most frequently occurring dementia in the presenile
population. Despite epidemiologic data showing that patients with FTD may have …
population. Despite epidemiologic data showing that patients with FTD may have …
Extracellular vesicles in Alzheimer's disease: friends or foes? Focus on aβ-vesicle interaction
P Joshi, L Benussi, R Furlan, R Ghidoni… - International journal of …, 2015 - mdpi.com
The intercellular transfer of amyloid-β (Aβ) and tau proteins has received increasing
attention in Alzheimer's disease (AD). Among other transfer modes, Aβ and tau …
attention in Alzheimer's disease (AD). Among other transfer modes, Aβ and tau …
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation
D Galimberti, C Fenoglio, M Serpente, C Villa… - Biological …, 2013 - Elsevier
Background A hexanucleotide repeat expansion in the first intron of C9ORF72 has been
shown to be responsible for a high number of familial cases of amyotrophic lateral sclerosis …
shown to be responsible for a high number of familial cases of amyotrophic lateral sclerosis …
Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration
J Goossens, M Bjerke, S Van Mossevelde… - Alzheimer's research & …, 2018 - Springer
Background We explored the diagnostic performance of cerebrospinal fluid (CSF)
biomarkers in allowing differentiation between frontotemporal lobar degeneration (FTLD) …
biomarkers in allowing differentiation between frontotemporal lobar degeneration (FTLD) …
Effect of the histone deacetylase inhibitor FRM-0334 on progranulin levels in patients with progranulin gene haploinsufficiency: a randomized clinical trial
PA Ljubenkov, L Edwards, L Iaccarino… - JAMA Network …, 2021 - jamanetwork.com
Importance Histone deacetylase inhibitors have been repeatedly shown to elevate
progranulin levels in preclinical models. This report describes the first randomized clinical …
progranulin levels in preclinical models. This report describes the first randomized clinical …
[HTML][HTML] CSF pro-orexin and amyloid-β38 expression in Alzheimer's disease and frontotemporal dementia
WE Heywood, J Hallqvist, AJ Heslegrave… - Neurobiology of …, 2018 - Elsevier
There is an unmet need for markers that can stratify different forms and subtypes of
dementia. Because of similarities in clinical presentation, it can be difficult to distinguish …
dementia. Because of similarities in clinical presentation, it can be difficult to distinguish …
Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentations
A Arighi, GG Fumagalli, F Jacini… - Journal of …, 2012 - content.iospress.com
A hexanucleotide repeat expansion in the first intron of C9ORF72 has been shown to be
responsible for a high number of familial cases of amyotrophic lateral sclerosis or …
responsible for a high number of familial cases of amyotrophic lateral sclerosis or …