Abnormal eye movement in patients with spinocerebellar ataxia type 3 (Machado-Joseph disease)
Author:
Affiliation:
1. Department of Oto-neurology, Tokyo Metropolitan Neurological Hospital
2. Medical Corporation Saikeikai
Publisher
Japan Society of Equilibrium Research
Subject
Clinical Neurology,Otorhinolaryngology
Reference24 articles.
1. 1) Nakano KK, Dawson DM, Spence A: Machado disease; a hereditary ataxia in Portuguese emigrants to Massachusetts. Neurology 22: 49-55, 1972
2. 2) Lima L, Coutinho P: Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorean Portuguese family. Neurology 30: 319-322, 1980
3. 3) Spinella GM, Sheridan PH: Research initiatives on Machado-Joseph disease: national institute of neurological disorders and stroke workshop summary. Neurology 42: 2048-2051, 1992
4. 4) Coutinho P, Andrade C: Autosomal dominant system degeneration in Portuguese families of the Azores Islands: a new genetic disorder involving cerebellar, pyramidal, extrapyramidal, and spinal cord motor functions. Neurology 28: 703-709, 1978
5. 5) Healton EB, Brust JCM, Kerr DL, et al.: Presumably Azorean disease in a presumably non-Portuguese family. Neurology 30: 1084-1089, 1980
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1. Spinocerebellar Degeneration (SCD);Equilibrium Research;2023-08-31
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