Results 181 to 190 of about 16,223 (208)
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The neuropathology of progressive supranuclear palsy

1994
The macroscopical, histological, ultrastructural and immunocytochemical features of progressive supranuclear palsy (PSP) are reviewed. Recent investigations have revealed important differences in the distribution, ultrastructure and immunocytochemical profile of neurofibrillary tangles in PSP and in Alzheimer's disease.
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Update on progressive supranuclear palsy

Current Neurology and Neuroscience Reports, 2004
A better understanding of the challenges in the diagnosis of progressive supranuclear palsy (PSP), the most common atypical parkinsonian neurodegenerative disorder, has led to improving its diagnostic accuracy. Similarly, a better understanding of the role of tau mutations, mitochondrial complex I inhibitors, oxidative injury, and inflammation in ...
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The Epidemiology of Progressive Supranuclear Palsy

2008
Publisher Summary This chapter describes that the incidence of progressive supranuclear palsy (PSP) is approximately 1 per 100,000 and the prevalence is approximately 5 per 100,000. Most patients ascertained by such community-based surveys were not previously diagnosed as having PSP, testament to the low sensitivity to the diagnosis on the part of ...
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Progressive Supranuclear Palsy: an Update

Current Neurology and Neuroscience Reports, 2018
Progressive supranuclear palsy (PSP) is a 4R tau neuropathologic entity. While historically defined by the presence of a vertical supranuclear gaze palsy and falls in the first symptomatic year, clinicopathologic studies identify alternate presenting phenotypes.
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[Sleep in progressive supranuclear palsy].

Rivista di patologia nervosa e mentale, 1982
Nocturnal sleep was poligraphycally recorded in three male patients aged 54-67, with progressive supranuclear palsy (PSP). All patients suffered from insomnia. In case 1 REM sleep was markedly reduced and spindles were less numerous than in normal subjects.
Massetani R   +4 more
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Neuropathology of Progressive Supranuclear Palsy

2008
Publisher Summary This chapter describes progressive supranuclear palsy (PSP) as an atypical parkinsonian disorder associated with progressive axial rigidity, vertical gaze palsy, dysarthria, and dysphagia. A frontal lobe syndrome and subcortical dementia are present in some cases.
openaire   +2 more sources

Clinical Conditions “Suggestive of Progressive Supranuclear Palsy”—Diagnostic Performance

Movement Disorders, 2020
John Van Swieten   +2 more
exaly  

Prediagnostic Progressive Supranuclear Palsy – Insights from the UK Biobank

Parkinsonism and Related Disorders, 2022
James Rowe   +2 more
exaly  

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