Figure 3.

FTLD-Tau. Inclusions in progressive supranuclear palsy (A,B), corticobasal degeneration (C), white matter tauopathy with globular glial inclusions (D), argyrophilic grain disease (E), and Pick’s disease (F). Progressive supranuclear palsy, corticobasal degeneration, white matter tauopathy with globular glial inclusions and argyrophilic grain disease are four-repeat tauopathies with abundant neuronal and glial tau filaments. Pick’s disease is a three-repeat tauopathy with abundant neuronal tau filaments. Scale bar, 50 µm.