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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.
Comprehensive characterization and optimization of anti-LRRK2 (leucine-rich repeat kinase 2) monoclonal antibodies
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
