TRIM25 mutation (p.C168*), coding for an E3 ubiquitin ligase, is a cause of early-onset autosomal dominant dementia with amyloid load and parkinsonism
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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
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Brain - ISSN 0006-8950-146:4 (2023) p. 1624-1636
Improved Alzheimer's disease versus frontotemporal lobar degeneration differential diagnosis combining EEG and neurochemical biomarkers : a pilot study
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Journal of Alzheimer's disease - ISSN 1387-2877-90:4 (2022) p. 1739-1747
How network-based approaches can complement gene identification studies in frontotemporal dementia
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Trends in genetics - ISSN 0168-9525-38:9 (2022) p. 944-955
Protein interaction network analysis reveals genetic enrichment of immune system genes in frontotemporal dementia
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Neurobiology of aging - ISSN 0197-4580-116 (2022) p. 67-79