Therapeutic Interventions in the Primary Hereditary Ataxias
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology
Link
http://link.springer.com/content/pdf/10.1007/s11940-010-0075-8.pdf
Reference55 articles.
1. Finsterer J: Ataxias with autosomal, X-chromosomal or maternal inheritance. Can J Neurol Sci 2009, 36:409–428. This is an excellent recent review of the inherited ataxias, most notable for its thoroughness and numerous useful summary tables. The author also presents an interesting synthesized classification of ataxias based on phenotypic groups.
2. Bürk K, Mälzig U, Wolf S, et al.: Comparison of three clinical rating scales in Friedreich ataxia (FRDA). Mov Disord 2009, 24:1779–1784.
3. Friedman LS, Farmer JM, Perlman S, et al.: Measuring the rate of progression in Friedreich ataxia: implications for clinical trial design. Mov Disord 2010, 25:426–432. The natural history of Friedreich’s ataxia is being studied prospectively by a multicenter collaborative research team in the United States, and this report outlines the 2-year data from a cohort of 236 patients. Such data are crucial for designing future treatment trials.
4. Schmitz-Hübsch T, Coudert M, Bauer P, et al.: Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms. Neurology 2008, 71:982–989. This paper explores the covariance of disease factors on disease severity, and found that SCA6 tends to act differently than SCA1, 2, and 3.
5. Perlman SL: Cerebellar ataxia. Curr Treat Options Neurol 2000, 2:215–224.
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