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Olivopontocerebellar atrophy (Menzel Type)
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Familial ataxia with extreme difference in age of clinical onset
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Olivopontocerebellar atrophy: A review of 117 cases
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Cerebellar and brainstem hypometabolism in olivopontocerebellar atrophy detected with positron emission tomography
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A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy
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R.C. Duvoisin, A. Plaitakis. Raven Press, New York
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[10] Wadia, N.H. (1984) A variety of olivopontocerebellar atrophy distinguished by slow eye movements and peripheral neuropathy. In the olivopontocerebellar atrophies. In: R.C. Duvoisin, A. Plaitakis. Raven Press, New York, pp. 149-177.
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Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy
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Morphological changes of olivopontocerebellar atrophy in computed tomography and comments on its pathogenesis
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R.C. Duvoisin and A. Plaitakis. Raven Press, New York
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[12] Huang, Y.P., Plaitakis, A. (1984) Morphological changes of olivopontocerebellar atrophy in computed tomography and comments on its pathogenesis. In: R.C. Duvoisin and A. Plaitakis, The olivopontocerebellar atrophies. Raven Press, New York, pp. 39-85.
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Computerized tomography and auditory evoked potentials: Use in the diagnosis of olivopontocerebellar degeneration
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The trinucleotide repeat expansion of chromosome 6p (SCA 1) in autosomal dominant cerebellar ataxias
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