Results 181 to 190 of about 16,224 (212)
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Progressive supranuclear palsy on Guam
Acta Neuropathologica, 2001This is the first report demonstrating that progressive supranuclear palsy (PSP) exists on Guam. This 75-year-old Guamanian Chamorro patient with slight dementia and rigidity with restriction of ocular up gaze was diagnosed as parkinsonism-dementia complex (PDC) of Guam clinically.
M, Yamazaki +6 more
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Caregiving in progressive supranuclear palsy
Neurology, 1998Basic issues regarding factors influencing progressive supranuclear palsy (PSP) patient caregiver burden remain unresolved, including whether and how disease severity and duration influence caregiver burden.To examine the relation between PSP patient caregiver burden and disease severity, describe the time course of caregiver burden in relation to ...
B, Uttl +3 more
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Tremor in progressive supranuclear palsy
Acta Neurologica Scandinavica, 1989Reports of tremor in progressive supranuclear palsy (PSP) have been infrequent; some authors indicate that tremor is never seen in PSP. Five patients with PSP and tremor are presented. Our series of cases and those reviewed in the literature suggest that tremor occurs in 12-16% of PSP cases. The rest tremor observed in 3 of our cases differed from the "
E F, Masucci, J F, Kurtzke
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Genetics of progressive supranuclear palsy
2008Publisher Summary This chapter emphasizes that progressive supranuclear palsy (PSP) is the second most common form of degenerative parkinsonism and is characterized clinically by an akinetic-rigid syndrome, supranuclear gaze palsy, pseudobulbar signs, and cognitive decline of frontal lobe type.
Alan, Pittman +3 more
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The neuropathology of progressive supranuclear palsy
1994The 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, 2004A 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
2008Publisher 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, 2018Progressive 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, 1982Nocturnal 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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