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Quoted phrase not found in phrase index: "Jerky ocular pursuit movements"
Page 1
Neurovisual profile in children affected by Angelman syndrome.
Galli J, Loi E, Strobio C, Micheletti S, Martelli P, Merabet LB, Pasini N, Semeraro F, Fazzi E; AS Collaborative Group. Galli J, et al. Brain Dev. 2023 Feb;45(2):117-125. doi: 10.1016/j.braindev.2022.10.003. Epub 2022 Nov 4. Brain Dev. 2023. PMID: 36344336
RESULTS: All children had visual impairments mainly characterized by refractive errors, ocular fundus changes, strabismus, discontinuous/jerky smooth pursuit and altered saccadic movements, and/or reduced visual acuity. ...Moreover, subjects with a chr …
RESULTS: All children had visual impairments mainly characterized by refractive errors, ocular fundus changes, strabismus, discontinu …
Oculomotor abnormalities in Friedreich's ataxia.
Kirkham TH, Guitton D, Katsarkas A, Kline LB, Andermann E. Kirkham TH, et al. Can J Neurol Sci. 1979 May;6(2):167-72. doi: 10.1017/s0317167100119584. Can J Neurol Sci. 1979. PMID: 487305
The defects comprised square wave jerks, jerky pursuit with inability to maintain eccentric gaze resulting in gaze paretic nystagmus and rebound nystagmus. There was failure to suppress by fixation the vestibulo-ocular reflex. The slow phase velocity of calor …
The defects comprised square wave jerks, jerky pursuit with inability to maintain eccentric gaze resulting in gaze paretic nys …
Joubert's syndrome: new cases and review of clinicopathologic correlation.
Sztriha L, Al-Gazali LI, Aithala GR, Nork M. Sztriha L, et al. Pediatr Neurol. 1999 Apr;20(4):274-81. doi: 10.1016/s0887-8994(98)00154-4. Pediatr Neurol. 1999. PMID: 10328276
All patients had severe developmental delay, hypotonia, impairment of smooth visual pursuit, and saccadic eye movements. Six had jerky eye movements and ptosis was observed in two patients and retinal dystrophy in one. ...Abnormal cerebellar-brainstem …
All patients had severe developmental delay, hypotonia, impairment of smooth visual pursuit, and saccadic eye movements. Six h …
Spinocerebellar ataxia type 17: extension of phenotype with putaminal rim hyperintensity on magnetic resonance imaging.
Loy CT, Sweeney MG, Davis MB, Wills AJ, Sawle GV, Lees AJ, Tabrizi SJ. Loy CT, et al. Mov Disord. 2005 Nov;20(11):1521-3. doi: 10.1002/mds.20529. Mov Disord. 2005. PMID: 16037935
We report on a 50-year-old woman who presented with an 8-year history of involuntary movements, unsteadiness, and cognitive decline. Examination revealed multidomain cognitive deficits, jerky ocular pursuit movements, hypometric saccades, gaze i …
We report on a 50-year-old woman who presented with an 8-year history of involuntary movements, unsteadiness, and cognitive decline. …