Development of Postrotatory Nystagmus Time Constants

References

• Änggård L. An electrophysiological study of the development of cochlear functions in the rabbit. Acta Otolaryngol (Stockh) 1965, Suppl. 203: 1
   Google Scholar
• Anniko M. Embryologic development in vivo and in vitro of the dark cell region of the mammalian crista ampullaris. Acta Otolaryngol (Stockh) 1980; 90: 106
   PubMed Web of Science ®Google Scholar
• Anniko M., Bagger-Sjöbäck D. Maturation of junctional complexes during embryonic and early postnatal development of inner ear secretory epithelia. Am J Otolaryngol 1982; 3: 242
   PubMed Web of Science ®Google Scholar
• Anniko M., Nordemar H. Formation of the cupular crista ampullaris: Development in vivo and in vitro. Am J Otolaryngol 1980; 3: 31
   Google Scholar
• Anniko M., Wroblewski R. Elemental composition of the developing inner ear. Ann Otol Rhinol Laryngol 1981; 90: 25
   PubMed Web of Science ®Google Scholar
• Anniko M., Sobin A., Wroblewski R. X-ray microanalysis of inner ear fluids in the embryonic and newborn guinea pig. Arch Otorhinolaryngol 1982; 234: 125
   PubMedGoogle Scholar
• Babin R. W., Ryu J. H., McCabe B. F. Second-order vestibular adaptation and cupular dynamics. Ann Otol 1980; 89: 262
   Google Scholar
• Babin R. W., Ryu J. H., McCabe B. F. Second-order neural responses after contralateral vestibular nerve sectioning. Am J Otolaryngol 1983; 4: 101
   PubMedGoogle Scholar
• Bast T. H., Anson B. J. The Temporal Bone and the Ear. C. C. Thomas, Springfield, Ill 1949
   Google Scholar
• Blanks R. H. I., Estes M. S., Markham C. H. Physiologic characteristics of vestibular first-order canal neurons in the cat. II. Response to constant angular acceleration. J Neurophysiol 1975; 38: 1250
   PubMed Web of Science ®Google Scholar
• Brument N., Pujol R., Sans A., Marty R. Maturation epitheliale des recepteurs dans l'oreille interne du chat. C R Soc Biol (Paris) 1969; 163: 688
   Google Scholar
• Collins W. E. Arousal and vestibular habituation. Vestibular System. Part 2. Psychophysics, Applied Aspects and General Interpretations, H. H. Kornhuber. Springer-Verlag, New York 1974; 361
   Google Scholar
• Cordero L., Clark D. L., Urrutia J. G. Post-rotatory nystagmus in the full term and premature infant. Int J Ped Otorhinolaryngol 1983; 5: 47
   PubMedGoogle Scholar
• Hallpike C. S., Hood J. D. The speed of the slow component of ocular nystagmus induced by angular acceleration of the head: Its experimental determination and application to the physical theory of the cupular mechanism. Proc Roy Soc (Biol) 1953; 141: 216
   PubMed Web of Science ®Google Scholar
• Heywood P., Pujol R., Hilding D. A. Development of the labyrinthine receptors in the guinea pig, cat and dog. Acta Otolaryngol (Stockh) 1976; 82: 359
   PubMed Web of Science ®Google Scholar
• Hoshino T. Scanning electron microscopic observation of the foetal labyrinthine vestibule. Acta Otolaryngol (Stockh) 1982; 93: 349
   PubMed Web of Science ®Google Scholar
• Jones G. M., Spells K. E. A theoretical and comparative study of the functional dependence of the semicircular canal upon its physical dimensions. Proc Roy Soc (Lond) 1963; 157: 403
   PubMed Web of Science ®Google Scholar
• Malcolm R. A quantitative study of vestibular adaptation in human. Fourth Symposium on the Role of the Vestibular Organs in Space Exploration. Pensacola, Fla. 1970; 369, NASA SP-187
   Google Scholar
• Malcolm R. Adaptation of the vestibulo-ocular system to rotation. Adv Oto-Rhino-Laryngol 1973; 19: 120
   PubMedGoogle Scholar
• Malcolm R., Melville-Jones G. A quantitative study of vestibular adaptation in humans. Acta Otolaryngol (Stockh) 1970; 70: 126
   PubMed Web of Science ®Google Scholar
• Markham C. H., Yagi T., Curthoys I. S. The contribution of the contralateral labyrinth to second order vestibular neuron activity in the cat. Brain Res 1977; 138: 99
   PubMed Web of Science ®Google Scholar
• Marquardt D. M. An algorithm for least squares estimation of nonlinear parameters. J Indust Appl Math 1963; 11: 431
   Web of Science ®Google Scholar
• Mikaelian D., Ruben R. J. Development of hearing in the normal CBA-J mouse. Correlation of physiological observations with behavioral responses and with cochlear anatomy. Acta Otolaryngol (Stockh) 1965; 59: 451
   Google Scholar
• Ornitz E. M., Atwell C. W., Walter D. O., Hartmann E. E., Kaplan A. R. The maturation of vestibular nystagmus in infancy and childhood. Acta Otolaryngol (Stockh) 1979; 88: 244
   PubMed Web of Science ®Google Scholar
• Robinson D. A. Models of oculomotor neural organization. The Control of Eye Movements, P. Bach-y-Rita, C. C. Collins. Academic Press, New York 1971
   Google Scholar
• Schmid R. M. Systems analysis of the vestibulo-ocular system. Fifth Symposium on the Role of Vestibular Organs in Space Exploration. Pensacola, Fla. 1970; 237, NASA SP-314
   Google Scholar
• Schmid R. M., Stefanelli M., Mira E. Mathematical modeling. A contribution to clinical vestibular analysis. Acta Otolaryngol (Stockh) 1971; 72: 292
   PubMed Web of Science ®Google Scholar
• Sills A. W., Honrubia V., Baloh R. W. Is the adaptation model a valid description of the vestibulo-ocular reflex?. Biol Cybernetics 1978; 30: 209
   PubMedGoogle Scholar
• Sills A. W., Honrubia V. A new method for determining impulsive time constants and their application to clinical data. Otorhinolaryngology 1978; 86: 81
   Google Scholar
• van Egmond A. A. J., Groen J. J., Jongkees L. B. W. The mechanics of the semicircular canal. J Physiol 1949; 110: 1
   PubMed Web of Science ®Google Scholar
• van Egmond A. A. J., Groen J. J., Jongkees L. B. W. The function of the vestibular organ. Pract ORL 1952; 14(Suppl. 2)
   Google Scholar
• Young L. R., Oman C. M. A model for vestibular adaptation to horizontal rotation. The Role of the Vestibular Organs in Space Exploration. Pensacola, Fla. 1970; 363, NASA SP-187
   Google Scholar