Results 231 to 240 of about 34,277 (277)

Diffusion tensor imaging of sequential neuropathological patterns in progressive supranuclear palsy. [PDF]

open access: yesFront Aging Neurosci
Bârlescu LA   +8 more
europepmc   +1 more source

Data-driven modelling of tau pathology reveals distinct progressive supranuclear palsy subtypes

open access: yes
Cullinane PW   +25 more
europepmc   +1 more source

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 ...
Loretta, Mazorra, Mary P, Cadogan
core   +8 more sources

Progressive supranuclear palsy

Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova, 2021
Progressive supranuclear palsy (PSP) is a heterogeneous progressive neurodegenerative disease characterized by onset after 50 years old, Parkinson's syndrome, early development of postural instability, absence or transient reaction to levodopa drugs, neuropsychological disorders, dysphagia and dysarthria and eye movement disorders.
N V, Fedorova   +3 more
openaire   +3 more sources

Progressive Supranuclear Palsy

Archives of Neurology, 1982
To the Editor.— I appreciated the letter to the editor "Progressive Supranuclear Palsy Despite Normal Eye Movements" by Dr Nuwer (Archives1981;38:784). In the case reported by Dr Nuwer, the diagnosis was supported by electronystagmography, which showed typical changes, and pneumoencephalography, which demonstrated pontine and midbrain atrophy ...
G W, Hynd, F J, Pirozzolo, G J, Maletta
  +7 more sources

PROGRESSIVE SUPRANUCLEAR PALSY

Age and Ageing, 1977
In 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
openaire   +2 more sources

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