Functional Consequences of Oculomotor Disorders in Hereditary Cerebellar Ataxias
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s12311-012-0433-z.pdf
Reference40 articles.
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3. Klostermann W, Zühlke C, Heide W, et al. Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1. J Neurol. 1997;244:105–11.
4. Buttner N, Geschwind D, Jen JC, et al. Oculomotor phenotypes in autosomal dominant ataxias. Arch Neurol. 1998;55:1353–7.
5. Rivaud-Pechoux S, Dürr A, Gaymard B, et al. Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I. Ann Neurol. 1998;43:297–302.
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