References
- Abrahams V. C., Rose P. K. Projections of extraocular, neck muscle, and retinal afferent* to superior colliculus in the cat: their connections to cells of origin of tectospinal tract. J. Neurophvsiol 1975; W: 10–18
- Bach-Y-Rita P. Properties of stretch receptors in cat extraocular muscles. J. Physiol 1966; 186: 663–688
- Batini C., Buisseret P., Kado R. T. Extraocular proprioceptive and trigeminal projections to the Purkinje cells of the cerebellar cortex. Arch. Hal. Biol 1974; 7/2: 1–17
- Buisseret P., Maffei L. Extraocular proprioceptive projections to the visual cortex. Exp. Brain Res 1977; 28: 421–425
- Collins C. C. Orbital mechanics. The Control of Eve Movement, P. Bach-y-Rita, C. C. Collins, J. E. Hyde. Academic Press Inc., New York/London 1971; 283–326
- Cooper S., Fillenz M. Afferent discharges in response to stretch from the extraocular muscles of the cat and monkey and the innervation of these muscles. J. Physio 1955; 27: 400–4l3
- Donaldson I. M.L. Responses in cat suprasylvian cortex (Clare Bishop Area) to stretch of extraocular muscles. J Physiol 1979; 2: 60–61
- Donaldson I. M.L., Dixon R. A. Excitation of units in the lateral geniculate and contiguous nuclei of the cat by stretch of extrinsic ocular muscle. Exp. Brain Res 1980; W: 245–255
- Donaldson I. M.L., Long A. C. Suppression of visual responses in the cat superior couiculus following stretch of extraocular muscles. J. Physiol 1977; 272: 94–95
- Donaldson I. M.L., Long A. C. Interactions between extraocular proprioceptive and visual signals in the superior coUiculus of the cat. J. Physiol 1980; 2W: 85–110
- Enomoto H. Projections of extraocular muscle afferents to visual cortex in the cat. I. Cell tvoes in visual cortex responsible for afferent impulses evoked bv oculomotor nerve stimulation. Acta Soc. Ophlhal Jpn 1982; 86: 687–694
- Fuchs A. F., Kornhuber H. H. Extraocular muscle afferents to the cerebellum of the cat. J. Phvsiol 1969; 200: 713–722
- Ikeda H. Visual acuity, its development and amblyopia. J roy. Soc. Med 1980; 73: 546–555
- Ikeda H., Tremain K. E. The development of spatial resolving power of LGN cells and its susceptibility to blur and strabismus. Arch. Hal. Biol 1978; 116: 375–384
- Ikeda H., Tremain K. E. Amblyopia occurs in retinal ganglion cells in cats reared with convergent squint without alternating fixation. Exp. Brain Res 1979; 35: 559–582
- Ikeda H., Wright M. J. Retinotopic distribution, visual latency and orientation tuning of “sustained” and ‘transient’ cortical neurones in area 17 of the cat. Exp. Brain Res 1975; 22: 385–398
- Maekawa K., Kimura M. Mossy fiber projections to the cerebellar flocculus from the extraocular muscle afferents. Brain Res 1980; 191: 313–325
- Maier A., Desant1s M., Eldred E. The occurrence of muscle spindles in extraocular muscles of various vertebrates. J. Morphol 1974; 143: 397–408
- Nikara T., Bishop P. O., Pettigrew J. D. Analysis of retinal correspondence by studying receptive fields of binocular single units in cat striate cortex. Exp. Brain Res 1968; 6: 353–372
- Noda H., Freeman R. B., Creutzfeldt O. D. Neuronal correlates of eye movements in the visual cortex of the cat. Science 1972; 75: 66l–664
- Rose P. K., Abrahams V. C. Effect of passive eye movements on unit discharge in the superior coUiculus of the cat. Brain Res 1975; 97: 95–106
- Tomlinson R. D., Schwarz D. W.F. Response of oculomotor neurons to eye muscle stretch. Canad. J. Phvsiol. Pharmacol 1977; 55: 568–573