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Progressive Supranuclear Palsy [PDF]

open access: yesParkinsonism & Related Disorders, 2012
Progressive supranuclear palsy (PSP) is a neurodegenerative tauopathy which can manifest clinically in a variety of syndromes. In this review, the classic and most common variant syndrome -PSP-Richardson's syndrome (PSP-RS) -is the focus, with the core clinical features, varying cognitive/motor/neuropsychiatric/sleep manifestations, neuropsychological ...
Hoelzle, James B
core   +10 more sources

Zolpidem in Progressive Supranuclear Palsy [PDF]

open access: yesCase Reports in Neurological Medicine, 2013
Progressive supranuclear palsy (PSP) is a progressive neurodegenerative disorder, characterized by motor symptoms, postural instability, personality changes, and cognitive impairment. There is no effective treatment for this disorder.
Sandip K. Dash
doaj   +4 more sources

Emerging Hypersexuality in a Patient With Progressive Supranuclear Palsy [PDF]

open access: yesBJPsych Open
Aims: Progressive supranuclear palsy (PSP) typically presents with a constellation of motor symptoms, most commonly with frequent falls and gait disturbances.
Pei Ling Lim, Boon Ceng Chai
doaj   +2 more sources

Genetics of Progressive Supranuclear Palsy [PDF]

open access: yesJournal of Movement Disorders, 2015
Progressive supranuclear palsy (PSP) is a neurodegenerative syndrome that is clinically characterized by progressive postural instability, supranuclear gaze palsy, parkinsonism and cognitive decline.
Sun Young Im   +2 more
doaj   +3 more sources

Clinical Approach to Progressive Supranuclear Palsy [PDF]

open access: yesJournal of Movement Disorders, 2016
Sixty years ago, Steele, Richardson and Olszewski designated progressive supranuclear palsy (PSP) as a new clinicopathological entity in their seminal paper. Since then, in addition to the classic Richardson’s syndrome (RS), different clinical phenotypic
Helen Ling
doaj   +5 more sources

Progressive supranuclear palsy [PDF]

open access: yesPostgraduate Medical Journal, 2000
Abstract Progressive supranuclear palsy (PSP) or Steele-Richardson-Olszewski syndrome is a neurodegenerative disease of middle and late age. It is under-diagnosed not only by general physicians but also by neurologists. The cause of PSP is not known.
Lyndon C. Wong, Becky R. Lowrey
  +8 more sources

Progressive supranuclear palsy [PDF]

open access: yesSeminars in Neurology, 2001
Unfortunately, no drug treatment has been shown to benefit patients with progressive supranuclear palsy (PSP) more than modestly or briefly. The multiplicity of neuronal systems and synaptic physiologies that degenerate in this disorder makes a neurotransmitter-specific approach, such as neurotransmitter replacement or reuptake inhibition, unlikely to ...
D B Ramsden, K Tawana
openaire   +8 more sources

Clinical Features of Patients With Progressive Supranuclear Palsy in an US Insurance Claims Database

open access: yesFrontiers in Neurology, 2021
Background: Progressive supranuclear palsy is a rare neurodegenerative movement disorder and little is known about its epidemiology.Objective: Estimate age-adjusted prevalence of progressive supranuclear palsy and describe antecedent diagnoses and ...
Emma Viscidi   +11 more
doaj   +1 more source

Umbilical cord blood stem cells transplantation in a patient with severe progressive supranuclear palsy: a case report

open access: yesJournal of Medical Case Reports, 2021
Background Progressive supranuclear palsy is a neurodegenerative condition that worsens over time. Given the lack of targeted treatments, patients with severe progressive supranuclear palsy have very low life expectancy.
Huiping Li   +7 more
doaj   +1 more source

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

open access: yes, 2020
Background: The Movement Disorder Society diagnostic criteria for progressive supranuclear palsy introduced the diagnostic certainty level “suggestive of progressive supranuclear palsy” for clinical conditions with subtle signs, suggestive of the disease.
Arzberger, T. (T.)   +19 more
core   +4 more sources

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