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Progressive supranuclear palsy
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Medical condition of the brain
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atypical progressive supranuclear palsy syndrome
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12
Prevalence of heterozygous mutations in Niemann-Pick type C genes in a cohort of progressive supranuclear palsy
scientific article published on 18 August 2020
Atypical progressive supranuclear palsy with corticospinal tract degeneration
scientific article
Clinical and neuropathologic features of progressive supranuclear palsy with severe pallido-nigro-luysial degeneration and axonal dystrophy
article
Looking into the prediagnostic phase of progressive supranuclear palsy
scientific article published on 15 April 2020
Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration
scientific article
Divergent brain gene expression patterns associate with distinct cell-specific tau neuropathology traits in progressive supranuclear palsy
article
Cognitive decline on the Repeatable Battery for the Assessment of Neuropsychological Status in progressive supranuclear palsy
scientific article published on 27 September 2019
Cognitive deficits in progressive supranuclear palsy on the Repeatable Battery for the Assessment of Neuropsychological Status
scientific article published on 04 February 2019
A clinicopathological study of vascular progressive supranuclear palsy: a multi-infarct disorder presenting as progressive supranuclear palsy
scientific article
Diagnostic accuracy of progressive supranuclear palsy in the Society for Progressive Supranuclear Palsy brain bank
scientific article
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Progressive supranuclear palsy (PSP) is a late-onset neurodegenerative disease involving the gradual deterioration and death of specific volumes of the brain, linked to 4-repeat tau pathology. The condition leads to symptoms including loss of balance, slowing of movement, difficulty moving the eyes, and cognitive impairment. PSP may be mistaken...

Instance of
designated intractable/rare disease
Rare disease
class of disease
Subclass of
Movement disorder
eye degenerative disease
Disease
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