Results 71 to 80 of about 1,100,883 (182)

The phenotypic spectrum of progressive supranuclear palsy.

, 2016
Traditionally, the clinical picture of progressive supranuclear palsy (PSP) was defined by early postural instability with falls, supranuclear vertical gaze palsy, symmetric akinesia and rigidity, frontal and subcortical dementia, and pseudobulbar palsy,
Respondek, G;Höglinger, G U
core   +1 more source

Supranuclear Vertical Gaze Disorders

, 1978
Upward Gaze Palsy - easily overlooked. Bilateral: Parinaud\u27s Syndrome, Sylvian Aqueduct Syndrome.
Shirley H. Wray, MD, PhD, FRCP
core  

Clinical Correlation Between Vertical Gaze Palsy and Midbrain Volume in Progressive Supranuclear Palsy

, 2022
Background: Supranuclear vertical gaze palsies and slowed vertical saccades are characteristic clinic features of progressive supranuclear palsy (PSP).
Karen A. Buch; Marc A. Bouffard; Randy H. Kardon; Anne-Marie A. Wills; Claudio M. Privitera; Mansi Sharma; Shirley H. Wray
core  

How breathing disrupts vision: hyperventilation‐induced hypocapnia impairs oculomotor responses in resting humans

The Journal of Physiology, Volume 604, Issue 5, Page 2336-2354, 1 March 2026.
Abstract figure legend Hypocapnic hyperventilation reduced end‐tidal carbon dioxide partial pressure and middle cerebral artery mean velocity, and impaired oculomotor response by modulating visual fixation and anti‐saccadic control. Hyperventilation itself also impaired anti‐saccadic control.
Yusei Yoshimura, Tomoka Sagawa, Seiji Ono, Takeshi Nishiyasu, Naoto Fujii   +4 more
wiley   +1 more source

Parkinsonism: heterogeneity of a common neurological syndrome

Swiss Medical Weekly, 2011
Parkinsonism refers to a neurological syndrome embracing bradykinesia, muscle rigidity, tremor at rest and impaired postural reflexes, and involving a broad differential diagnosis.
G Kaegi
doaj   +1 more source

Apraxia in progressive nonfluent aphasia [PDF]

, 2010
The clinical and neuroanatomical correlates of specific apraxias in neurodegenerative disease are not well understood. Here we addressed this issue in progressive nonfluent aphasia (PNFA), a canonical subtype of frontotemporal lobar degeneration that has
Rohrer, J.D., Rossor, M.N., Warren, J.D.
core  

The Importance of Neuropathology in a Complex Movement Disorder with Primary Familial Brain Calcification

Movement Disorders, Volume 41, Issue 6, Page 1600-1601, June 2026.
Ida Gugler, Per Svenningsson, Inger Nennesmo, Martin Paucar   +3 more
wiley   +1 more source

RECOMMENDATIONS ON DIAGNOSTICS AND TACTICS OF MANAGEMENT OF NIEMANN-PICK DISEASE, TYPE C

Педиатрическая фармакология, 2012
Niemann–Pick disease, type C (NP-C), is a rare hereditary neurovisceral disease caused by mutations in either the NPC1 gene (in 95% of cases) or the NPC2 gene (ca.
L. M. Kuzenkova, L. S. Namazova-Baranova, A. K. Gevorkyan, T. V. Podkletnova, A. M. Mamedyarov   +4 more
doaj   +1 more source

Associations between neuropsychological profile and regional brain FDG uptake in progressive supranuclear palsy

Journal of Parkinson’s Disease
Background Progressive supranuclear palsy (PSP) is a rare neurodegenerative movement disorder clinically characterized by falls, axial rigidity, vertical supranuclear gaze palsy, bradykinesia, and cognitive decline. There is a relative lack of studies on
Johanna Doll-Lee, Martin Klietz, Stephan Greten, Bruno Kopp, Georg Berding, Matthias Brendel, Ida Wilkens, Sabrina Katzdobler, Johannes Levin, Adrian Danek, Sophia Rogozinski, Günter Höglinger, Monika Pötter-Nerger, Carsten Buhmann, Ralph Buchert, Florian Wegner,   +16 more
doaj   +1 more source

Quality of life in patients with progressive supranuclear palsy: a review of literature and implications for practice

Frontiers in Neurology
Progressive supranuclear palsy (PSP) is an atypical form of parkinsonism characterized by tauopathy, manifesting as oculomotor dysfunction, postural instability, akinesia, and cognitive/language impairments.
Michał Markiewicz, Natalia Madetko-Alster, Piotr Alster   +2 more
doaj   +1 more source