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Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Heritability and genetic variance of dementia with Lewy bodies
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
Exome sequencing reveals VCP mutations as a cause of familial ALS
Cerebrospinal fluid biomarker signature in Alzheimer's disease neuroimaging initiative subjects
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy
Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein
Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
TDP-43 pathologic lesions and clinical phenotype in frontotemporal lobar degeneration with ubiquitin-positive inclusions
