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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.
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
Lewy body disease is a contributor to logopenic progressive aphasia phenotype
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
