Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.-Reference-Cited by-同舟云学术

Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.

Published:1984-01-01 Issue:1 Volume:47 Page:21-25
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Baraitser M,Gooddy W,Halliday A M,Harding A E,Rudge P,Scaravilli F

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference15 articles.

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4. Progressive myoclonus epilepsy. A clinical and histopathological study;Koskiniemi, M.; Donner, M.; Majuri, H.; Haltia, M.; Norio, R.;Acta Neurol Scand,1974

5. Progressive myoclonus and epilepsy with dentatorubral degeneration;Bird, T.D.; Shaw, C.M.;J Neurol Neurosurg Psychiatry,1978

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1. A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot-Marie-Tooth disease;Clinical Genetics;2008-06-28

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3. Autosomal dominant cerebellar ataxia deafness and narcolepsy;Journal of the Neurological Sciences;1995-12

4. References;Metabolic and Degenerative Diseases of the Central Nervous System;1995

5. Reflex myoclonus in olivopontocerebellar atrophy.;Journal of Neurology, Neurosurgery & Psychiatry;1994-03-01