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    <title>Wentzel, P.R.</title>
    <link>http://repub.eur.nl/res/aut/21244/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Ultrastructure of projections to the oculomotor nucleus and inferior olive from vestibular and cerebellar neurons involved in compensatory eye movements (Doctoral Thesis)</title>
      <link>http://repub.eur.nl/res/pub/17659/</link>
      <pubDate>1998-06-17T00:00:00Z</pubDate>
      <description>Early in the evolution of vertebrates eye movements were strictly primitive reflexes that
were predominantly controlled by vestibular and visual sensory stimuli. Later during
phylogeny, along with the development of the fovea of the retina, vertebrates acquired the
ability to make voluntary eye movements (BOttner and BUttner-Eonever, 1988). In short, five
types of eye movements can be distinguished. The first two are slow eye movements that
compensate for movements of the head and the visual surround; these are named the vestibuloocular
reflex (VOR) and the optokinetic reflex (OKR), respectively. Extended rotatory or
visual stimulation results in a so-called vestibular or optokinetic nystagmus with a slow
(compensatory) and a fast (reset) phase. The eye movements that operate predominantly under
voluntary control are saccades, smooth pursuit, and convergence. Saccadic eye movements are
fast conjugate eye movements which reset the eye position; smooth pursuit movements are
used to follow a small moving visual target; and convergence movements are slow
disconjugate eye movements enabling frontal-eyed animals to foveate near objects and establish
stereoscopic vision.</description>
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