Associated Papers
ANXA11 Mutations in the FTD Spectrum: A Novel Finding in a Patient With Semantic Variant Primary Progressive Aphasia.
Meng Y et al.
European Journal of Neurology, 2025
40345169 (PubMed )
Supplement: ENE-32-e70187-s001.docx
Disparate and shared transcriptomic signatures associated with cortical atrophy in genetic behavioral variant frontotemporal degeneration.
Shen T et al.
Molecular Neurodegeneration, 2025
39920674 (PubMed )
Supplement: 13024_2025_806_MOESM1_ESM.pdf
Case report: TMEM106B haplotype alters penetrance of GRN mutation in frontotemporal dementia family.
Perneel J et al.
Frontiers in Neurology, 2023
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.
Moore KM et al.
The Lancet. Neurology, 2020
31810826 (PubMed )
Supplement: NIHMS1067362-supplement-Supplement.pdf
Frontotemporal dementia spectrum: first genetic screen in a Greek cohort.
Ramos EM et al.
Neurobiology of Aging, 2019
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