Progressive supranuclear palsy: diagnosis, pathology, and therapy.

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Progressive supranuclear palsy: what do we know about it?

Progressive supranuclear palsy (PSP) is a progressive tauopathy characterized by supranuclear ophthalmoplegia, pseudobulbar palsy, dysarthria, axial rigidity, frontal lobe dysfunction, and dementia. The typical pathology includes neuronal loss, gliosis and microtubule-associated protein tau (MAPT)-positive inclusions in neurons and glial cells, primarily in basal ganglia, brainstem and cerebell...

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Progressive supranuclear palsy: clinical features, pathophysiology and management.

Progressive supranuclear palsy (PSP) is a degenerative condition of unknown aetiology that produces an akinetic-rigid form of parkinsonism characterised by early falls and abnormalities of extraocular movements. Mean age of onset is approximately 63 years, and mean survival from symptom onset is 9 years. Men are much more frequently affected than women. The classic clinical finding is supranucl...

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SHORT REPORT Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsy

Background: Most magnetic resonance imaging (MRI) studies of progressive supranuclear palsy (PSP) are crosssectional and lack post mortem confirmation of the diagnosis. MRI features described previously in PSP correspond to regions of pathological involvement demonstrated in separate studies, but serial MRI with pathological follow up has not been undertaken. Objective: To investigate whether r...

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Pathological substrate for regional distribution of increased atrophy rates in progressive supranuclear palsy.

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عنوان ژورنال:
  • Journal of neural transmission. Supplementum

دوره 42  شماره 

صفحات  -

تاریخ انتشار 1994