Associated Papers
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.
Pottier C et al.
Nature Communications, 2025
40280976 (PubMed )
Supplement: 41467_2025_59216_MOESM3_ESM.xlsx › SD26
Clinical and neuroanatomical characterization of the semantic behavioral variant of frontotemporal dementia in a multicenter Italian cohort.
Ghirelli A et al.
Journal of Neurology, 2024
38597943 (PubMed )
Supplement: 415_2024_12338_MOESM1_ESM.docx
A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease.
Tacik P et al.
Journal of Neuropathology and Experimental Neurology, 2015
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