Background Frontotemporal dementia is a highly heritable neurodegenerative disorder. In
about a third of patients, the disease is caused by autosomal dominant genetic mutations …

Background Frontotemporal dementia is a heterogenous neurodegenerative disorder, with
about a third of cases being genetic. Most of this genetic component is accounted for by …

Several micro (mi) RNA are deregulated in brain, cerebrospinal fluid (CSF), and serum/plasma
from patients with Alzheimer's disease (AD). The aim of the study was to profile …

Frontotemporal dementia (FTD) is a highly heritable condition with multiple genetic causes.
In this study, similarities and differences of gray matter (GM) atrophy patterns were assessed …

Background and Objectives The goal of this work was to investigate the natural history and
outcomes after treatment for spontaneous amyloid-related imaging abnormalities (ARIA)-like …

Background Neurofilament light chain (NfL) is a promising blood biomarker in genetic
frontotemporal dementia, with elevated concentrations in symptomatic carriers of mutations in GRN…

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 or …

The early differential diagnosis of Parkinson's disease (PD) and atypical Parkinsonian
syndromes (APS), including corticobasal degeneration (CBD) and progressive supranuclear …

Alzheimer’s disease (AD) is the most common cause of neurodegenerative dementia, whilst
Parkinson’s disease (PD) is a neurodegenerative movement disorder. These two …

Small extracellular vesicles (EVs) are able to pass from the central nervous system (CNS)
into peripheral blood and contain molecule markers of their parental origin. The aim of our …