The development of symmetrical OKN in infants: Quantification based on OKN acuity for nasalward versus temporalward motion

Vision Research

Volumn 40, Issue 4, 2000, Pages 445-453

  Lewis, Terri L ^a   Maurer, Daphne ^a   Chung, Joanna Y Y ^a   Holmes Shannon, Rebecca ^a   Van Schaik, Charmaine S ^a  

^a MCMASTER UNIVERSITY   (Canada)

Author keywords

Acuity; Development; Infant vision; Monocular optokinetic nystagmus asymmetries; Optokinetic nystagmus; Spatial frequency

Indexed keywords

AGE; ARTICLE; CONTROLLED STUDY; EYE DEVELOPMENT; EYE MOVEMENT; HUMAN; HUMAN EXPERIMENT; INFANT; NORMAL HUMAN; OPTOKINETIC NYSTAGMUS; PATHOGENESIS; PRESCHOOL CHILD; PRIORITY JOURNAL; SPATIAL FREQUENCY DISCRIMINATION; VISUAL ACUITY;

CHILD DEVELOPMENT; CHILD, PRESCHOOL; HUMANS; INFANT; NYSTAGMUS, OPTOKINETIC; VISION, MONOCULAR; VISUAL CORTEX; VISUAL PATHWAYS;

EID: 0033989591     PISSN: 00426989     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0042-6989(99)00190-X     Document Type: Article

References (59)

1. Abadai R.V., Howard I.P., Ohmi M., Howard T., Lee E.E., Wright M.J. The rise time and steady-state gain of the human optokinetic response (OKR). Investigative Ophthalmology and Visual Science. 35:1994;2035. (abstract).
2. Abadai R.V., Pantazidou M. Monocular optokinetic nystagmus in humans with age-related maculopathy. British Journal of Ophthalmology. S1:1997;123-129.
3. Abadi R.V., Pascal E. The effects of simultaneous central and peripheral field motion on the optokinetic response. Vision Research. 31:1991;2219-2225.
4. Atkinson J. Development of optokinetic nystagmus in the human infant and monkey infant: an analogue to development in kittens. Freeman R.D. Developmental neurobiology of vision. 1979;277-287 Plenum, New York.
5. Atkinson J., Braddick O. Development of optokinetic nystagmus in infants: an indicator of cortical binocularity? Fisher D.G., Monty R.A., Senders J.W. Eye movements: cognition and visual perception. 1981;53-64 Erlbaum, Hillsdale, NJ.
6. Braddick O. Motion processing: where is the nave-temporal asymmetry? Current Biology. 6:1996;250-253.
7. Braddick O., Atkinson J., Hood B. Striate cortex, extrastriate cortex, and colliculus: some new approaches. Vital-Durand F., Atkinson J., Braddick O.J. Infant vision. 1996;203-220 Oxford University Press, Oxford.
8. Braddick O., Mercuri E., Atkinson J., Wattem-Bell J. Basis of the nave-temporal asymmetry in infants VEPs to grating displacements. Investigative Ophthalmology and Visual Science. 39:1998;S884.
9. Braun J.J., Gault F.P. Monocular and binocular control of horizontal optokinetic nystagmus in cats and rabbits. Journal of Comparative and Physiological Psychology. 69:1969;12-16.
10. Brown R.J., Wilson J.R., Norcia A.M., Boothe R.G. Development of directional motion symmetry in the monocular visually evoked potential of infant monkeys. Vision Research. 38:1998;1253-1263.
11. Chugani H. Development of regional brain glucose metabolism in relation to behavior and plasticity. Dawson G., Fisher K. Human behavior and the developing brain. 1994;153-175 Guilford Press, New York.
12. Cohen B., Matsuo V., Raphan T. Quantitative analysis of the velocity characteristics of optokinetic nystagmus and optokinetic after-nystagmus. Journal of Physiology (London). 270:1977;321-344.
13. Cohen B., Reisine H., Yokota J.I., Raphan T. The nucleus of the optic tract. Its function in gaze stabilization and control of visual-vestibular interaction. Annals of the New York Academy of Science. 656:1992;277-296.
14. Cohen B., Schiff D., Buettner J. Contribution of the nucleus of the optic tract to optokinetic nystagmus and optokinetic after nystagmus in the monkey: clinical implications. Cohen B., Bodis-Wollner I. Vision and the brain. 1990;233-255 Raven, New York.
15. Harris L.R., Leporé F., Guillemot J.P., Cynader M. Abolition of optokinetic nystagmus in the cat. Science. 210:1980;91-92.
16. Harris L.R., Lewis T.L., Maurer D. Brain stem and cortical contributions to the generation of horizontal optokinetic eye movements in humans. Visual Neuroscience. 10:1993;247-259.
17. Hatta S., Kumagami T., Qian J., Thorton M., Smith E.L. III, Chino Y.M. Nasotemporal directional bias of V1 neurons in young infant monkeys. Investigative Ophthalmology and Visual Science. 39:1998;2259-2267.
18. Hoffmann K.-P. Cortical versus subcortical contributions to the optokinetic reflex in the cat. Lennerstrand G., Keller E.L. Functional basis of ocular motility disorders. 1982;303-310 Pergamon, New York.
19. Hoffmann K.-P. Visual inputs relevant for the optokinetic nystagmus in mammals. Progress in Brain Research. 64:1986;75-84.
20. Hoffmann K.-P. Functional organization in the optokinetic system of mammals. Rahman H. Progress in zoology: neuronal plasticity and brain function. 1989;261-271 Fisher, New York.
21. Hoffmann K.-P., Distler C., Erickson R. Functional projections from striate cortex and superior temporal sulcus to the nucleus of the optic tract (NOT) and dorsal terminal nucleus of the accessory optic tract (DTN) of macaque monkeys. Journal of Comparative Neurology. 313:1991;707-724.
22. Hoffmann K.-P., Distler C., Erickson R.G., Mader W. Physiological and anatomical identification of the nucleus of the optic tract and dorsal terminal nucleus of the accessory optic tract in monkeys. Experimental Brain Research. 69:1988;635-644.
23. Howard I.P., Ohmi M. The efficiency of the central and peripheral retina in driving human optokinetic nystagmus. Vision Research. 24:1984;969-976.
24. Howell D.C. Statistical methods for psychology. 2nd edn:1987;Duxbury Press, Boston.
25. Huttenlocher P.R. Synaptogenesis in human cerebral cortex. Dawson G., Fischer K. Human behavior and the developing brain. 1994;137-152 Guilford Press, New York.
26. Kato I., Harada K., Hasegawa T., Igarashi T., Koike Y., Kawasaki T. Role of the nucleus of the optic tract in monkeys in relation to optokinetic nystagmus. Brain Research. 364:1986;12-22.
27. Kirk R.E. Experimental design. 2nd edn:1982;Wadsworth, Belmont.
28. Krementizer J.P., Vaughan H.G., Kurtzberg D., Dowling K. Smooth-pursuit eye movements in the newborn infant. Child Development. 50:1979;442-448.
29. Lewis T.L., Maurer D. The development of the temporal and nasal visual fields during infancy. Vision Research. 32:1992;903-911.
30. Lewis T.L., Maurer D., Brent H.P. The development of visual resolution in infants and toddlers tested monocularly with optokinetic nystagmus. Clinical Vision Sciences. 5:1990;231-241.
31. Lewis T.L., Maurer D., Brent H.P. The development of grating acuity in children treated for unilateral or bilateral congenital cataract. Investigative Ophthalmology and Visual Science. 36:1995;2080-2095.
32. Lewis T.L., Maurer D., Smith R.J., Haslip J.K. The development of symmetrical optokinetic nystagmus during infancy. Clinical Vision Sciences. 7:1992;211-218.
33. Mason A.J.S., Braddick O.J., Wattam-Bell J., Atkinson J. Directional motion asymmetry in infant VEPs - which direction? Investigative Ophthalmology and Visual Science. 39:1998;S1090.
34. Maurer D., Lewis T.L. Visual outcomes after infantile cataract. Simons K. Early visual development: normal and abnormal. Committee on Vision, Commission on Behavioral and Social Sciences and Education, National Research Council. 1993;454-484 Oxford University Press, Oxford.
35. Maurer D., Lewis T.L. Overt orienting toward peripheral stimuli: normal development and underlying mechanisms. Richards J.E. Cognitive neuroscience of attention: a developmental perspective. 1998;51-102 Erlbaum, Mahwah, NJ.
36. Montarolo P.G., Precht W., Strata P. Functional organization of the mechanism subserving the optokinetic nystagmus in the cat. Neuroscience. 6:1981;231-246.
37. Naegele J.R., Held R. The postnatal development of monocular optokinetic nystagmus in infants. Vision Research. 22:1982;341-346.
38. Naegele J.R., Held R. Development of optokinetic nystagmus and effects of abnormal visual experience during infancy. Jeannerod M., Hein A. Spatially oriented behavior. 1983;155-174 Springer-Verlag, New York.
39. Norcia A.M., Garcia H., Humphry R., Holmes A., Hamer R.D., Orel-Bixler D. Anomalous motion VEPs in infants and in infantile esotropia. Investigative Ophthalmology and Visual Science. 32:1991;436-439.
40. Pasik T., Pasik P. Optokinetic nystagmus: an unlearned response altered by section of chiasma and corpus callosum in monkeys. Nature. 203:1964;609-611.
41. Roy M.S., Lachapelle P., Leporé F. Maturation of the optokinetic nystagmus as a function of the speed of stimulation in fullterm and preterm infants. Clinical Vision Sciences. 4:1989;357-366.
42. Ryan T.A. Significance tests for multiple comparison of proportions, variances, and other statistics. Psychological Bulletin. 57:1960;318-328.
43. Schiff D., Cohen B., Raphan T. Nystagmus induced by stimulation of the nucleus of the optic tract in the monkey. Experimental Brain Research. 70:1988;1-14.
44. Schor C.M., Levi D.M. Disturbance of small-field horizontal and vertical optokinetic nystagmus in amblyopia. Investigative Ophthalmology and Visual Science. 19:1980;668-683.
45. Schor C., Narayan V. The influence of field size upon the spatial frequency response of optokinetic nystagmus. Vision Research. 21:1981;985-994.
46. Siegel S. Nonparametric statistics for the behavioral sciences. 1956;McGraw-Hill, New York.
47. Simpson J.I., Giolli R.A., Blanks R.H.I. The pretectal nuclear complex and the accessory optic system. Buttner-Ennever J.A. Neuroanatomy of the oculomotor system. 1988;335-364 Elsevier, New York.
48. Smith A.T., Harris L.R. Use of plaid patterns to distinguish the corticofugal and direct retinal inputs to the brainstem optokinetic nystagmus generator. Experimental Brain Research. 86:1991;324-332.
49. Strong N., Malach R., Lee P., Van Sluyters R.C. Horizontal optokinetic nystagmus in the cat: recovery from cortical lesions. Developmental Brain Research. 13:1984;179-192.
50. Teller D.Y., Succop A., Mar C. Infant eye movement asymmetries: stationary counterphase gratings elicit temporal-to-nasal optokinetic nystagmus in two-month-old infants under monocular test conditions. Vision Research. 33:1993;1859-1864.
51. van Die G.C., Collewijn H. Control of human optokinetic nystagmus by the central and peripheral retina: effects of partial visual field masking, scotopic vision and central retinal scotoma. Brain Research. 383:1986;185-194.
52. van Hof-van Duin J. Direction preference of optokinetic responses in monocularly tested normal kittens and light-deprived cats. Archives Italiennes de Biologie. 116:1978;471-477.
53. van Hof-van Duin J., Mohn G. Vision in the preterm infant. Prechtl H.F.R. Continuity of neural functions from prenatal to postnatal life. 1984;93-115 Lippincott, Philadelphia.
54. van Hof-van Duin J., Mohn G. The development of visual functions in preterm infants. Ergebaisse der Experimentellen Medizin. 46:1985;350-361.
55. van Hof-van Duin J., Mohn G. Visual field measurements, optokinetic nystagmus and the visual threatening response: normal and abnormal development. Documenta Ophthalmologica Proceedings Series. 45:1986;305-316.
56. Waespe W., Cohen B., Raphan T. Role of the flocculus in optokinetic nystagmus and visual-vestibular interaction: effects of flocculectomy. Experimental Brain Research. 50:1983;9-33.
57. Williams R.W., Chalupa L.M. Development of the retinal pathway to the pretectum of the cat. Neuroscience. 10:1983;1249-1267.
58. Zee D.S., Tusa R.J., Herdman S.J., Butler P.H., Gücer G. The acute and chronic effects of bilateral occipital lobectomy upon eye movements in monkey. Keller E.L., Zee D.S. Adaptive processes in visual and oculomotor systems. 1986;267-274 Pergamon, New York.
59. Zee D.S., Tusa R.J., Herdman S.J., Butler P.H., Gücer G. Effects of occipital lobectomy upon eye movements in the primate. Journal of Neurophysiology. 58:1987;883-907.