Ratings
0
Nobody has rated this yet. Be the first!
Works
7
Population studies of sporadic cerebral amyloid angiopathy and dementia: a systematic review.
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis
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.
