Hereditary Deafness in the Cat: An Electron Microscopic Study of the Spiral Ganglion

References

• Adamo N. J., Daigneault E. A. Ultrastructural features of neurons and nerve fibers in the spiral ganglia of cats. J Neurocytol 1973; 2: 91
   PubMedGoogle Scholar
• Ades H. W., Trahiotis C., Kokko-Cunningham A., Averbuch A. Comparison of hearing thresholds and morphological changes in the chinchilla after exposure to 4 kHz tones. Acta Otolaryngol (Stockh) 1974; 78: 192
   PubMed Web of Science ®Google Scholar
• Alexander G., Tandler J. Untersuchungen an kongenital tauben Hunden, Katzen und an Jungen kongenital tauber Katzen. Arch f Ohrenheilk 1905; 66: 161
   Google Scholar
• Awataguchi S., Nishimura T., Kon I., Ishida M., Yamamoto N. Submicroscopic studies on the spiral ganglion in guinea pigs. II. The transfiguration of the fine structures of the spiral ganglion exposed to the acoustic stimulation. Hirosaki Med J 1965; 17: 20
   Google Scholar
• Balentine J. D. Pathology of experimental spinal cord trauma. II. Ultrastructure of axons and myelin. Lab Invest 1978; 39: 254
   PubMed Web of Science ®Google Scholar
• Barron K. D., Dentinger M. P., Nelson L. R., Mincy J. E. Ultrastructure of axonal reaction in red nucleus of cat. J Neuropathol Exp Neurol 1975; 34: 222
   PubMedGoogle Scholar
• Bosher S. K., Hallpike C. S. Observations on the histological features, development and pathogenesis of the inner ear degeneration of the deaf white cat. Proc Roy Soc (Biol) 1965; 162: 147
   PubMed Web of Science ®Google Scholar
• Duchen L. W., Scaravilli F. Quantitative and electron microscopic studies of sensory ganglion cells of the Sprawling mouse. J Neurocytol 1977; 6: 465
   PubMedGoogle Scholar
• Elverland H. H., Mair I. W. S., Pedersen E. The primary afferent neurons in the hereditarily deaf white cat. INSERM 1977; 68: 67
   Google Scholar
• Engström H., Ades H. W., Anderson A. Structural Pattern of the Organ of Corti. Almqvist & Wik-sell, Stockholm 1966
   Google Scholar
• Fuentes C., Raymond J. Chromatolyse irréversible et dégénérescence rétrograde dans le ganglion vestibulaire. J Neurol Sci 1972; 17: 69
   PubMedGoogle Scholar
• Guillery R. W. Light- and electron-microscopical studies of normal and degenerating axons. Contemporary Research Methods in Neuroanatomy, W. J. H. Nauta, S. O. E. Ebbesson. Springer-Verlag, Berlin 1970; 77
   Google Scholar
• Gulley R. L., Wenthold R. J., Neises G. R. Change in the synapses of spiral ganglion cells in the rostral anteroventral cochlear nucleus of the waltzing guinea pig following hair cell loss. Brain Res 1978; 158: 279
   PubMedGoogle Scholar
• Howe H. A. The reaction of the cochlear nerve to destruction of its end organs: a study on deaf albino cats. J Comp Neurol 1935; 62: 73
   Google Scholar
• Jones E. G., Rockel A. J. Observations on complex vesicles, neurofilamentous hyperplasia and increased electron density during terminal degeneration in the inferior colliculus. J Comp Neurol 1972; 147: 93
   Google Scholar
• Kellerhals B., Engström H., Ades H. W. Die Morphologie des Ganglion spirale cochleae. Acta Otolaryngol (Stockh) 1967; 1, Suppl. 226
   PubMedGoogle Scholar
• Kerr A., Schuknecht H. F. The spiral ganglion in profound deafness. Acta Otolaryngol (Stockh) 1968; 65: 586
   PubMedGoogle Scholar
• Koch T., Schultz P., Williams R., Lampert P. Giant axonal neuropathy: a childhood disorder of microfilaments. Ann Neurol 1977; 1: 438
   PubMedGoogle Scholar
• Lim D. J. Ultrastructural cochlear changes following acoustic hyperstimulation and ototoxicity. Ann Otol Rhinol Laryngol 1976; 85: 740
   PubMed Web of Science ®Google Scholar
• Lindsay J. R. Profound childhood deafness. Ann Otol Rhinol Laryngol 1973; 82: 1, Suppl. 5
   Web of Science ®Google Scholar
• Mair I. W. S. Hereditary deafness in the white cat. Acta Otolaryngol (Stockh) 1973; 1, Suppl. 314
   Google Scholar
• Mair I. W. S., Elverland H. H. Hereditary deafness in the cat. An electron microscopic study of the stria vascularis and Reissner's membrane. Arch Oto-Rhino-Laryngol 1977; 217: 199
   PubMedGoogle Scholar
• Mair I. W. S., Elverland H. H., Laukii E. Development of early auditory-evoked responses in the cat. Audiology 1978; 17: 469
   PubMedGoogle Scholar
• Merck W., Riede U. N., Löhle E., Cürten I. Eine ultrastrukturell-morphometrische Analyse des Ganglion spirale cochleae des Meerschweinchens. Arch Oto-Rhino-Laryngol 1977; 214: 303
   PubMedGoogle Scholar
• Pujol R., Rebillard M., Rebillard G. Primary neural disorders in the deaf white cat cochlea. Acta Otolaryngol (Stockh) 1977; 83: 59
   PubMed Web of Science ®Google Scholar
• Raisman G., Matthews M. R. Degeneration and regeneration of synapses. The Structure and Function of Nervous Tissue, G. H. Bourne. Academic Press, New York and London 1972; vol. IV: 61
   Google Scholar
• Rosenbluth J. The fine structure of acoustic ganglia in the rat. J Cell Biol 1962; 12: 329
   PubMed Web of Science ®Google Scholar
• Rosenbluth J., Palay S. L. The fine structure of nerve cell bodies and their myelin sheaths in the eighth nerve ganglion of the goldfish. J Biophys Biochem Cytol 1961; 9: 853
   PubMedGoogle Scholar
• Ross M. D., Burkel W. Multipolar neurons in the spiral ganglion of the rat. Acta Otolaryngol (Stockh) 1973; 76: 381
   PubMed Web of Science ®Google Scholar
• Rossi G., Robecchi M. G., Penna M. Effects of acoustic trauma on Corti's ganglion. Acta Otolaryngol (Stockh) 1976; 81: 270
   PubMed Web of Science ®Google Scholar
• Schindler R. A., Björkroth B. Traumatic intra-cochlear electrode implantation. Laryngoscope 1979; 89: 752
   PubMedGoogle Scholar
• Schuknecht H. F. Lesions of the organ of Corti. Trans Am Acad Ophthalmol Otolaryngol 1953; 57: 366
   PubMedGoogle Scholar
• Smith C. A., Rasmussen G. L. Degeneration in the efferent nerve endings in the cochlea after axonal section. J Cell Bio 1965; 126: 63
   Google Scholar
• Spoendlin H. Degeneration behaviour of the coch-lear nerve. Arch Ohr-Nas-Kehlk Heilk 1971; 200: 275
   PubMedGoogle Scholar
• Spoendlin H. Neuroanatomy of the cochlea. Facts and Models in Hearing, E. Zwicker, E. Terhardt. Springer-Verlag, Berlin 1974; 18
   Google Scholar
• Spoendlin H. Retrograde degeneration of the cochlear nerve. Acta Orolaryngol (Stockh) 1975; 79: 266
   PubMed Web of Science ®Google Scholar
• Spoendlin H. The afferent innervation of the cochlea. Evoked Acrivity in the Audirory Nervous System, R. F. Naunton, C. Fernandez. Academic Press, New York 1978; 21
   Google Scholar
• Spoendlin H. Neural connections of the outer haircell system. Acta. Ofolaryngol (Stockh) 1979; 87: 381
   PubMed Web of Science ®Google Scholar
• Spoendlin H., Brun J.-P. The block-surface technique for evaluation of cochlear pathology. Arch Oto-Rhino-Laryngol 1974; 208: 137
   PubMedGoogle Scholar
• Spoendlin H., Gacek R. R. Electronmicroscopic study of the efferent and afferent innervation of the organ of Corti in the cat. Ann Otol Rhinol Laryngol 1963; 72: 660
   PubMed Web of Science ®Google Scholar
• Spoendlin H., Suter R. Regeneration in the eighth nerve. Acta Otolaryngol (Stockh) 1976; 81: 228
   PubMed Web of Science ®Google Scholar
• Thomsen E. The ultrastructure of the spiral ganglion in the guinea pig. Acta. Otolaryngol (Stockh) 1967; 442, Suppl. 224
   Google Scholar
• Torvik A. Phagocytosis of nerve cells during retrograde degeneration. J Neuroparh Exp Neurol 1972; 31: 132
   PubMedGoogle Scholar
• Ward W. D., Duvall A. J. Behavioural and ultra-structural correlates of acoustic trauma. Ann Otol Rhinol Laryngol 1971; 80: 881
   PubMed Web of Science ®Google Scholar
• Wright C. G. Neural damage in the guinea pig cochlea after noise exposure. Acta Otolaryngol (Stockh) 1976; 82: 82
   PubMed Web of Science ®Google Scholar
• Ylikoski J. Correlative studies on the cochlear pathology and hearing loss in guinea-pigs after intoxication with ototoxic antibiotics. Acta Orolaryngol (Stockh) 1974; 1, Suppl. 326
   Google Scholar