Associated Papers
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
Frequency of frontotemporal dementia-related gene variants in Turkey.
Artan S et al.
Neurobiology of Aging, 2021
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
Genetic predictors of survival in behavioral variant frontotemporal degeneration.
Caswell C et al.
Neurology, 2019
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
Chiang HH et al.
European Journal of Human Genetics : Ejhg, 2013
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