Cerebellar ataxia

Author:

Perlman Susan L.

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical)

Reference60 articles.

1. Mosely ML, Benzow KA, Schut LJ, et al.: Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology 1998, 51:1666–1671. This report demonstrates the power of the new molecular genetic diagnostic techniques and lays the groundwork for future gene-based therapies.

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3. Wexler ID, Hemalatha SG, McConnell J, et al.: Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutations. Neurology 1997, 49:1655–1661.

4. Steinberg D: Elucidation of the metabolic error in Refsum’s disease. Strategy and tactics. In The Inherited Ataxias. Edited by Kark RAP, Rosenberg RN, Schut LJ. New York: Raven Press; 1978:113–124.

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