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A Systematic Review of Apathy and Depression in Progressive Supranuclear Palsy
Journal of Geriatric Psychiatry and Neurology, 2021Depression and apathy can be significant problems in progressive supranuclear palsy (PSP). Using PRISMA guidelines, this systematic review examined prevalence estimates for depression and apathy in PSP, and, how different methods of definition may ...
Joshua Flavell, P. Nestor
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PROGRESSIVE SUPRANUCLEAR PALSY
Age and Ageing, 1977In the past four years, four patients with progressive supranuclear palsy have presented to the Department of Geriatric Medicine, Oxford, under the care of one of us (RAG). They were all females whose symptoms began in the sixth or seventh decade. They died from three to six years after the onset of symptoms. All had neuropathological studies which are
J A, Dalziel, R A, Griffiths
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Progressive Supranuclear Palsy
Science of Aging Knowledge Environment, 2004In this case study, we describe the symptoms, neurological examination, clinical course, and neuropathology of a patient with progressive supranuclear palsy (PSP). PSP is a relatively uncommon neurodegenerative disorder with many features similar to those of Parkinson's disease .
Michael, Pourfar, Jean-Paul, Vonsattel
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Progressive supranuclear palsy
2007![Graphic][1] A typical PSP patient. Note the marked reduction in facial expression and frontalis overactivity. Progressive supranuclear palsy (PSP) is a neurodegenerative disease, classified pathologically as a tauopathy, which all neurologists encounter from time to time.
Burn D, Lees A
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Progressive Supranuclear Palsy
The Neurologist, 2008Progressive supranuclear palsy (PSP) is the second most common cause of parkinsonism after Parkinson's disease (PD). The classic syndrome of PSP is widely recognized by neurologists as a combination of down gaze palsy with progressive rigidity and imbalance leading to falls.
Michael, Lubarsky, Jorge L, Juncos
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Four-Repeat Tau Seeding in the Skin of Patients With Progressive Supranuclear Palsy.
JAMA NeurologyThis study discusses 4-repeat tau seeding in the skin of patients with progressive supranuclear palsy.
Iván Martínez-Valbuena +4 more
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Progressive Supranuclear Palsy
Archives of Neurology, 1973Thirty-one electroencephalograms from 12 patients with progressive supranuclear palsy (PSP) were examined. Four patients had initially abnormal records. Five other patients had initially normal records, but all developed abnormalities during the follow-up period. Three of 12 patients had normal records; each of them had only one record taken.
P C, Su, E S, Goldensohn
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Progressive supranuclear palsy
Nursing Standard, 2013Progressive supranuclear palsy (PSP), or Steele-Richardson-Olszewski syndrome, is a rare, progressive neurodegenerative condition with cognitive and motor involvement. Diagnosis can be challenging as some people do not display the classic symptoms of the condition and there are no specific investigations to confirm diagnosis.
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Progressive supranuclear Palsy
Archiv f�r Psychiatrie und Nervenkrankheiten, 1971Es wird uber eine Beobachtung von „progressive supranuclear palsy“ berichtet, bei der die Erkrankung etwa mit 12 Jahren begann, uber 23 Jahre hin langsam progressiv verlief und die klinisch im wesentlichen durch eine parkinsonistische Symptomatik ausgezeichnet war. Anatomisch fand sich neben einer schweren Degeneration der S.
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PROGRESSIVE SUPRANUCLEAR PALSY
Medical Clinics of North America, 1999Richardson observed an unusual clinical syndrome in the 1950s, which he later designated progressive supranuclear palsy (PSP). Over the past 25 years, although knowledge of this disorder has gradually improved, its cause is still unknown, pathogenesis is unclear, and there is still no definitive treatment for this disorder.
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