However, other patients presented broad types of pathology, including pure nigral degeneration without any inclusions, MSA-like-synucleinopathy, PSP-like tauopathy, frontotemporal lobar degeneration with ubiquitin-positive-inclusions, and coexistence with TDP-43-positive inclusions. This evidence concerns the gene TARDBP and supranuclear palsy, progressive, 1.