References

References

• Ades H. W. A secondary acoustic area in the cerebral cortex of the cat. J. Neurophysiol. 1943; 6: 59–63
   Google Scholar
• Ades H. W. Midbrain auditory mechanisms in cats. J. Neurophysiol. 1944; 7: 415–424
   Google Scholar
• Ades H. W., Brookhart J. M. The central auditory pathway. J. Neurophysiol. 1950; 13: 189–205
   PubMed Web of Science ®Google Scholar
• Ades H. W., Mettleb F. A., Culler E. A. Effect of lesions in the medial geniculate bodies upon hearing in the cat. Am. J. Physiol. 1939; 125: 15–23
   Google Scholar
• Adrian E. D. Discharge frequencies in the cerebral and cerebellar cortex. J. Physiol. 1935; 82: 32–33
   Google Scholar
• Adrian E. D., Matthews B. H. C. The interpretation of potential waves in the cortex. J. Physiol. 1934; 81: 440–471
   PubMedGoogle Scholar
• Baknes W. T., Magoun H. W., Ranson S. W. The ascending auditory pathway in the brainstem of the monkey. J. comp. Neurol. 1943; 79: 129–152
   Google Scholar
• Bernhabd C. G., Taverner D., Widén L. Differences in the action of tubocurarin and strychnine on the spinal reflex excitability of the cat. Brit. J. Pharmacol. 1951; 6: 551–559
   Google Scholar
• Bishop G. H., o'leary J. L. Potentials near geniculate synapses. J. cell. comp. Physiol. 1942; 19: 315–331
   Google Scholar
• Bocca E. Notes on the innervation of the cochlea. Arch. Otolaryng. 1952; 55: 188–205
   Google Scholar
• Bornschein H., Gebnandt B. E. Selective removal of the nerve discharge component from the cochlear potential during anoxia. Acta Physiol. Scand. 1950; 21: 82–89
   Google Scholar
• Bremer F., Dow R. S. The cerebral acoustic area of the cat. A combined oscillographic and cytoarchitectonic study. J. Neurophysiol. 1939; 2: 308–318
   Google Scholar
• Bremee F. Analyse oscillographique des réponses sensorielles des écorces cérébrale et cérébelleuse. Rev. Neurol. 1952; 87: 65–92
   Google Scholar
• Bremee F. Les aires auditives de l'ecorce cérébrale. Imprimerie de Montligeon. 1952
   Google Scholar
• Bremee F. Some problems in neurophysiology. The Athlone Press, London 1953
   Google Scholar
• Bremer F., Gebnandt B. E. A micro‐electrode analysis of the acoustic response and the strychnine convulsive patterns of the cerebellum. Acta Physiol. Scand. 1954; 30: 120–136
   Google Scholar
• Brodal A., Jansen J. The ponto‐cerebellar projection in the rabbit and cat. J. comp. Neurol. 1945–46; 83–84; 31–118
   Google Scholar
• Brodal A., Tobvik A. Cerebellar projection of paramedian reticular nucleus of medulla oblongata in cat. J. Neurophysiol. 1954; 17: 484–495
   Google Scholar
• Brookhart J. M., Mobuzzi G., Snideb R. S. Spike discharges of single units in the cerebellar cortex. J. Neurophysiol. 1950; 13: 465–486
   Google Scholar
• Brookhart J. M., Mobuzzi G., Snideb R. S. Origin of cerebellar waves. J. Neurophysiol. 1951; 14: 181–190
   Google Scholar
• Cajal S., Ramòn Y. Histologie du système nerveux de l'homme et des vertébrés. Maloine, Paris 1909
   Google Scholar
• Hsiang‐Tung Chang. An observation on the effect of strychnine on local cortical potentials. J. Neurophysiol. 1951; 14: 22–28
   Google Scholar
• Hsiang‐Tung Chang. Dendritic potential of cortical neurons produced by direct electrical stimulation of the cerebral cortex. J. Neurophysiol. 1951; 14: 1–21
   Google Scholar
• Hsiang‐Tung Chang. Cortical response to stimulation of medullar pyramid in rabbit. J. Neurophysiol. 1955; 18: 332–352
   Google Scholar
• Combs M. C. Electro‐anatomical study of cerebellar localisation. Stimulation of various afferents. J. Neurophysiol. 1954; 17: 123–143
   Google Scholar
• Davies P. W. Effect of chloretone and negative spike response of cerebral cortex. Fed. Proc. 1952; 11: 30
   Google Scholar
• Davis H. The psychological phenomena of audition. Handbook of General Exp. Psychol. Clark Univ. Press, Worcester, Mass 1934; 962–998
   Google Scholar
• Davis H. Biophysics and physiology of the inner ear. Physiol. Rev. 1957; 37: 1–49
   PubMed Web of Science ®Google Scholar
• Dow R. S. Cerebellar action potentials in response to stimulation of various afferent connections. J. Neurophysiol. 1939; 2: 543–555
   Google Scholar
• Dow R. S. Cerebellar action potentials in response to stimulation of the cerebral cortex in monkeys and cats. J. Neurophysiol. 1942; 5: 121–136
   Google Scholar
• Dow R. S. Action potentials of cerebellar cortex in response to local electrical stimulation. J. Neurophysiol. 1949; 12: 245–256
   Google Scholar
• Evarts E. V. Effect of ablation prestriate cortex on auditory‐visual association in monkey. J. Neurophysiol. 1952; 15: 191–200
   Google Scholar
• Evarts E. V. Effect of auditory cortex ablation on auditory‐visual association in monkey. J. Neurophysiol. 1952; 15: 435–441
   Google Scholar
• Fernandez C. The innervation of the cochlea (Guinea Pig). Laryngoscope 1951; 61: 1152–1172
   PubMed Web of Science ®Google Scholar
• Forbes A. Problems of synaptic function. J. Neurophysiol. 1939; 2: 465–472
   Google Scholar
• Galambos R., Davis H. Inhibition of activity in single auditory nerve fibres by acoustic stimulation. J. Neurophysiol. 1944; 7: 287–303
   Google Scholar
• Galambos R., Davis H. Action potentials from single auditory nerve fibres. Science 1948; 108: 5, 513
   Google Scholar
• Galambos R., Rose J. E. Microelectrode studies on medial geniculate body of cat. I. Thalamic region activated by click stimuli. J. Neurophysiol. 1952; 15: 343–357
   Google Scholar
• Galambos R., Rose J. E. II. Response to clicks. J. Neurophysiol. 1952; 15: 359–380
   PubMed Web of Science ®Google Scholar
• Galambos R., Rose J. E. III. Response to pure tones. J. Neurophysiol. 1952; 15: 381–400
   PubMed Web of Science ®Google Scholar
• Galambos R., Rosenblith W. A. Brain stem response to acoustic stimuli. Electroenceph. Clin. Neurophysiol. 1949; 1: 254
   Google Scholar
• Galambos R., Rosenblith W. A., Rosenzweig M. R. Physiological evidence for a cochleo‐cochlear pathway in the cat. Experientia 1950; 6: 438–440
   Google Scholar
• Galambos R. Neural mechanism of audition. Physiol. Rev. 1954; 34: 497–528
   PubMed Web of Science ®Google Scholar
• Galambos R. Suppression of auditory nerve activity by stimulation of efferent fibres to the cochlea. Fed. Proc. 1955; 14: 53
   Google Scholar
• Galambos R. Suppression of auditory nerve activity by stimulation of efferent fibres to cochlea. J. Neurophysiol. 1956; 19: 424–437
   PubMed Web of Science ®Google Scholar
• Gernandt B. E. Hearing. Ann. Rev. Physiol. 1952; 14: 433–452
   Google Scholar
• Hallpike C. S., Rawdon‐Smith A. F. The Wever and Bray phenomen—a summary of the data concerning the origin of the cochlear effect. Ann. Otol. 1937; 46: 976–990
   Google Scholar
• Hampson J. L. Relationships between cat cerebral and cerebellar cortices. J. Neurophysiol. 1949; 12: 37–50
   PubMedGoogle Scholar
• Henneman E., Cooke P., Snider R. S. Cerebellar projections to the cerebral cortex in cat and monkey. Am. J. Physiol. 1948; 155: 443
   Google Scholar
• Hind J. E. An electrophysiological determination of tonotopic organisation in auditory cortex of cat. J. Neurophysiol. 1953; 16: 475–489
   Google Scholar
• Kemp E. H., Robinson E. H. Electric responses of the brain stem to bilateral auditory stimulation. Am. J. Physiol. 1937; 120: 316–322
   Google Scholar
• Kemp E. H., Coppée G. E., Robinson E. H. Electric responses of the brain stem to unilateral auditory stimulation. Am. J. Physiol. 1937; 120: 304–315
   Google Scholar
• Kryter K. A., Ades H. W. Studies on the function of the higher acoustic nervous centers in the cat. Am. J. Psychol. 1943; 56: 501–536
   Google Scholar
• Levi‐Montalcini R. The development of the acoustic‐vestibular centers in the chick embryo in the absence of the afferent root fibres and of descending fibre tracts. J. comp. Neurol. 1949; 91: 209–234
   PubMed Web of Science ®Google Scholar
• Lipman E. A. Acoustic function of the temporal cortex of the dog. Am. J. Psychol. 1949; 62: 215–227
   Google Scholar
• Lorente de Nó. Anatomy of the eighth nerve. Laryngoscope 1933; 43: 1–16
   Google Scholar
• Lorente de Nó. Anatomy of the eighth nerve. Laryngoscope 1933; 43: 327–350
   Google Scholar
• Lorente de Nó. Synaptic delay of motoneurons. Am. J. Physiol. 1935; 111: 272–282
   Google Scholar
• Lorente de Nó. A study of nerve physiology. Stud. Rockefeller Inst. Med. Res. 1947; Vol. 131–132
   Google Scholar
• Lorente de Nó. Conduction of impulses in the neurons of the oculomotor nucleus. 1953, Ciba Foundation Symp., the Spinal Cord. 132–179
   Google Scholar
• Magoun H. W. An ascending reticular activating system in the brain stem. Arch. Neurol. Psychiat. 1952; 67: 145–154
   PubMedGoogle Scholar
• Mettler F. A., et al. Acoustic value of the several components of the auditory pathway. Brain 1934; 57: 475–483
   Google Scholar
• Meyer D. R., Woolsey C. C. Effects of localised cortical destruction on auditory discriminative conditioning in cat. J. Neurophysiol. 1952; 15: 149–162
   Google Scholar
• Monnier M. Topographische Tafeln des Hirnstammes der Katze fur experimental‐physiologische Untersuchungen. Helv. Physiol. Acta 1943; 1: 437–449
   Google Scholar
• Portmann M. Les fibres nerveuses efferent cochleaires. Imprimerie‐librarie. Bordeaux 1952
   Google Scholar
• Pribham K. H., Rosner B. S., Rosenblith W. A. Electrical responses to acoustic clicks in monkey: Extent of neocortex activated. J. Neurophysiol. 1954; 17: 336–344
   Google Scholar
• Raab D. H., Ades A. W. Cortical and midbrain mediation of a conditioned discrimination of acoustic intensities. Am. J. Psychol. 1946; 59: 59–83
   PubMed Web of Science ®Google Scholar
• Rasmussen A. T. Studies of the VIIIth cranial nerve of man. Laryngoscope 1940; 50: 67–83
   Google Scholar
• Rasmussen G. L. The olivary peduncle and other fiber projections of the superior olivary complex. J. comp. Neurol. 1945–46; 83–84; 141–220
   Google Scholar
• Rasmussen G. L. Recurrent or ‘feed back’ connections of the auditory system of the cat. Anat. Rec. 1953; 115: 361
   Google Scholar
• Rasmussen G. L. Further observations of the efferent cochlear bundle. J. comp. Neurol. 1953; 99: 61–74
   PubMed Web of Science ®Google Scholar
• Rose J. E. The cellular structure of the auditory region of the cat. J. comp. Neurol. 1949; 91: 409–428
   PubMed Web of Science ®Google Scholar
• Rose J. E., Woolsey C. N. The relations of thalamic connections, cellular structure and evocable electrical activity in the auditory region of the cat. J. comp. Neurol. 1949; 91: 441–446
   Google Scholar
• Rosenzweig M. R., Sutton D. Binaural interaction in lateral lemniscus of cat. J. Neurophysiol. 1958; 21: 17–23
   PubMed Web of Science ®Google Scholar
• Scheibel M., Scheibel A., Mollica A., Moruzzi G. Convergence and interaction of afferent impulses on single units of reticular formation. J. Neurophysiol. 1955; 18: 308–331
   Google Scholar
• Snider R. S. Tactile auditory and visual areas in the cerebellum. Arch. Neurol. Psychiat. 1948; 60: 325–326
   Google Scholar
• Snider R. S. Recent contributions to the anatomy and physiology of the cerebellum. Arch. Neurol. Psychiat. 1950; 64: 196–219
   PubMedGoogle Scholar
• Snider R. S., Stowell A. Receiving areas of the tactile, auditory, and visual systems in the cerebellum. J. Neurophysiol. 1944; 7: 331–358
   Google Scholar
• Stakzl T. E., Taylor C. W., Magoun H. W. Collateral afferent excitation of reticular formation of brain stem. J. Neurophysiol. 1951; 14: 479–496
   Google Scholar
• Stotleh W. A. An experimental study of the cells and connections of the superior olivary complex of the cat. J. comp. Neurol. 1953; 98: 401–423
   Google Scholar
• Tasaki I. Nerve impulses in individual auditory nerve fibers of guinea pig. J. Neurophysiol. 1954; 17: 97–121
   PubMed Web of Science ®Google Scholar
• Tasaki I., Davis H. Electric responses of individual nerve elements in cochlear nucleus to sound stimulation (guinea pig). J. Neurophysiol. 1955; 18: 151–158
   PubMed Web of Science ®Google Scholar
• Thurlow W. K., Gross N. B., Kemp E. H., Lowy K. Microelectrode studies of neural auditory activity of cat. I. Inferior colliculus. J. Neurophysiol. 1951; 14: 289–304
   PubMed Web of Science ®Google Scholar
• Thurlow W. K., Gross N. B. II. Medial geniculate body. J. Neurophysiol. 1951; 14: 409–422
   Google Scholar
• Tuntturi A. R. Physiological determination on the boundary of the acoustic area in the cerebral cortex of the dog. Am. J. Physiol. 1950; 160: 395–401
   Google Scholar
• Tuntturi A. R. A difference in the representation of auditory signals for the left and right ears in the iso‐frequency contours of the right middle ectosylvian auditory cortex of the dog. Am. J. Physiol. 1952; 168: 712–727
   Google Scholar
• Tuntturi A. R. Effects of lesions of the auditory and adjacent cortex on conditioned reflexes. Am. J. Physiol. 1955; 181: 225–229
   Google Scholar
• Walker A. E. The projection of the medial geniculate body to the cerebral cortex in macaque monkey. J. Anat. (Lond.) 1937; 71: 319–331
   Google Scholar
• Waller W. H. Topographical relations of cortical lesions to thalamic nuclei in the albino rat. J. comp. Neurol. 1934; 60: 237–269
   Web of Science ®Google Scholar
• Van Eyck M. Contribution à l'étude de l'electrophysiologie de l'appareil vestibulaire. Acta oto‐rhino‐laryng. Belg. 1952; 6: 5–66
   Google Scholar
• Whitfield J. C. Electrophysiology of the central auditory pathway. Brit. Med. Bull. 1956; 12: 105–109
   PubMed Web of Science ®Google Scholar
• Winkler C., Potter A. Anatomical guide to experimental researches on the cat's brain. Wersluys, Amsterdam 1914
   Google Scholar
• Woollard H. H., Harpman J. A. The connection of the inferior colliculus and of the dorsal nucleus of the lateral lemniscus. J. Anat. 1939/40; 74: 441–458
   Google Scholar