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眼动系统控制模型与小脑:假说机制。

Ocular Motor System Control Models and the Cerebellum: Hypothetical Mechanisms.

机构信息

From the Daroff-Dell'Osso Ocular Motility Laboratory, Louis Stokes Cleveland Department of Veterans Affairs Medical Center and CASE Medical School; and the Department of Neurology, Case Western Reserve University and University Hospitals Case Medical Center, 10701 East Boulevard, Cleveland, OH, 44106, USA.

出版信息

Cerebellum. 2019 Jun;18(3):605-614. doi: 10.1007/s12311-018-1001-y.

DOI:10.1007/s12311-018-1001-y
PMID:30617628
Abstract

To review our studies and "top-down" models of saccadic intrusions and infantile nystagmus syndrome with the aim of hypothesizing areas of cerebellar connections controlling parts of the ocular motor subsystems involved in both types of function and dysfunction. The methods of eye-movement recording and modeling are described in detail in the cited references. Saccadic intrusions, such as square-wave jerks and square-wave oscillations, can be simulated by a single malfunction, whereas staircase saccadic intrusions required two independent malfunctions. The major infantile nystagmus syndrome waveforms are traceable to a failure to calibrate the damping ratio of the smooth pursuit system. The use of a behavioral ocular motor system model demonstrated how putative cerebellar dysfunctions could accurately simulate both the oscillations and the ocular motor responses seen in patients with both saccadic and pursuit disorders.

摘要

回顾我们关于扫视性闯入和婴儿型眼球震颤综合征的研究和“自上而下”模型,旨在假设控制与这两种功能和功能障碍相关的眼动子系统的小脑连接区域。眼球运动记录和建模的方法在引用的参考文献中详细描述。扫视性闯入,如方波急跳和方波摆动,可以通过单个故障来模拟,而阶梯式扫视性闯入则需要两个独立的故障。主要的婴儿型眼球震颤综合征波形可归因于未能校准平滑追踪系统的阻尼比。行为性眼动系统模型的应用表明,假定的小脑功能障碍如何能够准确地模拟在扫视和追踪障碍患者中看到的眼球运动反应和眼动性闯入。

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1
Ocular Motor System Control Models and the Cerebellum: Hypothetical Mechanisms.眼动系统控制模型与小脑:假说机制。
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2
Saccadic intrusions: review and update.扫视闯入:综述与更新。
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"Inverse latent" macro square-wave jerks and macro saccadic oscillations.“反向潜伏性” 宏观方波急跳和宏观眼球震颤
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引用本文的文献

1
Nystagmus only with fixation in the light: a rare central sign due to cerebellar malfunction.仅在光照下出现眼球震颤伴固定:罕见的因小脑功能障碍引起的中枢性体征。
J Neurol. 2022 Jul;269(7):3879-3890. doi: 10.1007/s00415-022-11108-9. Epub 2022 Apr 9.

本文引用的文献

1
Effects of topical brinzolamide on infantile nystagmus syndrome waveforms: eyedrops for nystagmus.局部布林佐胺对婴儿眼球震颤综合征波形的影响:用于眼球震颤的滴眼液。
J Neuroophthalmol. 2011 Sep;31(3):228-33. doi: 10.1097/WNO.0b013e318223d0a9.
2
Being "slow to see" is a dynamic visual function consequence of infantile nystagmus syndrome: model predictions and patient data identify stimulus timing as its cause.“视物迟缓”是婴儿型眼球震颤综合征的一种动态视觉功能后果:模型预测和患者数据表明刺激时机是其成因。
Vision Res. 2007 May;47(11):1550-60. doi: 10.1016/j.visres.2007.01.008. Epub 2007 Feb 27.
3
"Staircase" saccadic intrusions plus transient yoking and neural integrator failure associated with cerebellar hypoplasia: a model simulation.
“阶梯式”扫视侵入加短暂性联动及与小脑发育不全相关的神经整合功能障碍:模型模拟
Semin Ophthalmol. 2006 Oct-Dec;21(4):229-43. doi: 10.1080/08820530601006767.
4
Congenital nystagmus: hypotheses for its genesis and complex waveforms within a behavioral ocular motor system model.先天性眼球震颤:行为性眼动系统模型中其发生机制及复杂波形的假说
J Vis. 2004 Jul 27;4(7):604-25. doi: 10.1167/4.7.7.
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A hypothetical fixation system capable of extending foveation in congenital nystagmus.一种能够在先天性眼球震颤中延长注视的假想固定系统。
Ann N Y Acad Sci. 2002 Apr;956:608-10. doi: 10.1111/j.1749-6632.2002.tb02896.x.
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Neuropathology of Joubert syndrome.乔伯综合征的神经病理学
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Ocular and oculomotor signs in Joubert syndrome.乔伯综合征的眼部和眼球运动体征。
J Child Neurol. 1999 Oct;14(10):621-7. doi: 10.1177/088307389901401001.
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A new surgery for congenital nystagmus: effects of tenotomy on an achiasmatic canine and the role of extraocular proprioception.一种治疗先天性眼球震颤的新手术:腱切断术对无交叉犬的影响及眼外本体感觉的作用
J AAPOS. 1999 Jun;3(3):166-82. doi: 10.1016/s1091-8531(99)70063-7.
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The congenital and see-saw nystagmus in the prototypical achiasma of canines: comparison to the human achiasmatic prototype.犬类典型无交叉视神经中先天性和跷跷板样眼球震颤:与人类无交叉视神经原型的比较。
Vision Res. 1998 Jun;38(11):1629-41. doi: 10.1016/s0042-6989(97)00337-4.
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Myasthenia gravis: analog computer model.重症肌无力:模拟计算机模型
Exp Neurol. 1980 May;68(2):378-89. doi: 10.1016/0014-4886(80)90093-x.