Investigation of the role of miRNA variants in neurodegenerative brain diseases
Source
Frontiers in genetics - ISSN 1664-8021-16 (2025) p. 1-10
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia
Source
The American journal of human genetics - ISSN 0002-9297-111:7 (2024) p. 1316-1329
Subclinical epileptiform activity in the Alzheimer continuum : association with disease, cognition and detection method
Source
Alzheimer's research & therapy - ISSN 1758-9193-16:1 (2024) p. 1-20
TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism
Source
Alzheimer's & dementia - ISSN 1552-5260-19:7 (2023) p. 2805-2815
Patients carrying the mutation p.R406W in MAPT present with non-conforming phenotypic spectrum
Source
Brain - ISSN 0006-8950-146:4 (2023) p. 1624-1636