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A case of afferent neuropathy and deafness

Published online by Cambridge University Press:  29 June 2007

C. S. Hallpike
Affiliation:
Formerly Aural Physician and Director, Otological Research Unit, Medical Research Council, National Hospital, Queen Square, London, WC1 3BG.
D. G. F. Harrdiman
Affiliation:
Neuropathology Laboratory, General Infirmary, Leeds, LSI 3EX.
C. E. C. Wells
Affiliation:
Department of Neurology, University Hospital of Wales, Cardiff, CF4 4XW.

Abstract

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Type
Research Article
Copyright
Copyright © JLO (1984) Limited 1980

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References

REFERENCES

Blackwood, W. (1952) Biopsy technique in the diagnosis of peripheral neuropathies (especially hereditary and sensory neuropathy). Proceedings of the 1st International Congress of Neuropathology, Rome, 3, 415424.Google Scholar
Bogaert, L. Van, and Martin, L. (1974) Optic and cochleovestibular degenerations in the hereditaryataxias. I. Clinico-pathological and genetic aspects. Brain, 97, 1540.Google Scholar
Brain, Lord, and Wilkinson, M. (1965) Subacute cerebellar degeneration associated with neoplasms. Brain, 88, 465478.Google Scholar
Croft, P. B., Henson, R. A., Urich, H., and Wilkinson, P. C. (1965) Sensory neuropathy with bronchial carcinoma: a study of four cases showing serological abnormalities. Brain, 88, 501514.CrossRefGoogle ScholarPubMed
Denny-Brown, D. (1948) Primary sensory neuropathy with muscular changes associated with carcinoma. Journal of Neurology, Neurosurgery and Psychiatry, 11, 7387.CrossRefGoogle ScholarPubMed
Denny-Brown, D. (1951) Hereditary sensory radicular neuropathy. Journal of Neurology, Neurosurgery and Psychiatry, 14, 237252.CrossRefGoogle ScholarPubMed
Goldstein, N. P., Gibilisco, J. A., and Rushton, J. G. (1963) Trigeminal neuropathy and neuritis. A study of etiology with emphasis on dental causes. Journal of the American Medical Association, 184, 458462.CrossRefGoogle ScholarPubMed
Greenfield, J. G. (1954) The spino-cerebellar degenerations, p. 28. Blackwell Scientific Publications, Oxford.Google Scholar
Hallpike, C. S. (1967) Observations on the structural basis of two rare varieties of hereditary deafness. Myotatic, Kinesthetic and vestibular mechanisms, pp. 285289. Edited by de Reuck, A. V. S. and Knight, J.Churchill, London.Google Scholar
Hallpike, C. S., and Rawdon-Smith, A. F. (1935) The origin of the Wever and Bray phenomenon. Journal of Physiology, 83, 243254.Google Scholar
Harris, W. (1935) Paroxysmal neuralgic tic as a sequel of trigeminal neuritis. British Medical Journal, 1, 11121114.CrossRefGoogle ScholarPubMed
Henson, R. A., Hoffman, H. L., and Urich, H. (1965) Encephalomyelitis with carcinoma. Brain, 88, 449464.CrossRefGoogle ScholarPubMed
Henson, R. A., Russell, D. S., and Wilkinson, M. (1954) Carcinomatous neuropathy and myopathy. A clinical and pathological study. Brain, 77, 82121.Google Scholar
Hicks, E. P. (1922) Hereditary perforating ulcer of the foot. Lancet, 1, 319321.Google Scholar
Horowitz, S. H. (1974) Isolated facial numbness. Clinical significance and relation to trigeminal neuropathy. Annals of Internal Medicine, 80, 4953.Google Scholar
Jefferson, G. (1955) The trigeminal neurinomas with some remarks on malignant invasion of the gasserian ganglion. Clinical Neurosurgery, 1, 1154.Google Scholar
McGill, T. (1976) Carcinomatous encephalomyelitis with auditory and vestibular manifestations. Annals of Otology, Rhinology and Laryngology, 85, 120126.Google Scholar
Ohta, M., Ellefson, R. D., Lambert, E. H., and Dyck, P. J. (1973) Hereditary sensory neuropathy, type II. Clinical, electrophysiologic, histologic, and biochemical studies of a Quebec kinship. Archives of Neurology, 29, 2337.CrossRefGoogle Scholar
Olive, I., and Svien, H. J. (1957) Neurofibromas of the fifth cranial nerve. Journal of Neurosurgery, 14, 484504.CrossRefGoogle ScholarPubMed
Russell, D. S. (1961) Encephalomyelitis and ‘carcinomatous neuropathy’. Encephalitides, pp. 131135. Edited by Van Bogaert, L.Radermecker, J.Hozay, J. and Lowenthal, A.Elsevier, Amsterdam.Google Scholar
Spillane, J. D., and Wells, C. E. C. (1959) Isolated trigeminal neuropathy. A report of 16 cases. Brain, 82, 391416.CrossRefGoogle ScholarPubMed
Spoendlin, H. (1974) Optic and cochleovestibular degenerations in hereditary ataxias. II. Temporal bone pathology in two cases of Friedreich's ataxia with vestibulo-cochlear disorders. Brain, 97, 4148.Google Scholar
Stammers, F. A. R. (1930) A study of tumours and inflammations of the Gasserian ganglion. British Journal of Surgery, 18, 125153.Google Scholar
Subotić, R. (1976) Journal of Laryngology and Otology, 90, 174181.Google Scholar
Urich, H. (1976) Diseases of peripheral nerves. Greenfield's Neuropathology, chapter 16, pp. 688770. 3rd edition by Blackwood, W. and Corsellis, J. A. N.Arnold London.Google Scholar
Wilkinson, P. C., and Zeromski, J. (1965) Immunofluorescent detection of antibodies against neurones in sensory carcinomatous neuropathy. Brain, 88, 529538.Google Scholar
Wittmaack, J. (1911) Über sekundäre Degenerationen im inneren Ohre nach Akustikusstrangverletzungen. Verhandlungen der deutschen otologischen Gesellschaft, 20, 289295.Google Scholar