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Works
11
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
Lethal recessive myelin toxicity of prion protein lacking its central domain
Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies
Induction of tau pathology by intracerebral infusion of amyloid-beta -containing brain extract and by amyloid-beta deposition in APP x Tau transgenic mice
The propagation of prion-like protein inclusions in neurodegenerative diseases
Argyrophilic grain disease.
Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease
Transmission and spreading of tauopathy in transgenic mouse brain
Loss of hypocretin (orexin) neurons with traumatic brain injury
The molecular basis of frontotemporal dementia
