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Genetic cerebellar ataxias.
Storey E. Storey E. Semin Neurol. 2014 Jul;34(3):280-92. doi: 10.1055/s-0034-1386766. Epub 2014 Sep 5. Semin Neurol. 2014. PMID: 25192506 Review.
Spinocerebellar ataxia type 20.
Storey E, Gardner RJ. Storey E, et al. Handb Clin Neurol. 2012;103:567-73. doi: 10.1016/B978-0-444-51892-7.00038-3. Handb Clin Neurol. 2012. PMID: 21827916 Review.
Role of proteolysis in polyglutamine disorders.
Tarlac V, Storey E. Tarlac V, et al. Among authors: storey e. J Neurosci Res. 2003 Nov 1;74(3):406-16. doi: 10.1002/jnr.10746. J Neurosci Res. 2003. PMID: 14598317 Review.
Spinocerebellar ataxia type 15.
Storey E, Gardner RJ. Storey E, et al. Handb Clin Neurol. 2012;103:561-5. doi: 10.1016/B978-0-444-51892-7.00037-1. Handb Clin Neurol. 2012. PMID: 21827915 Review.
A functional MRI study of motor dysfunction in Friedreich's ataxia.
Akhlaghi H, Corben L, Georgiou-Karistianis N, Bradshaw J, Delatycki MB, Storey E, Egan GF. Akhlaghi H, et al. Among authors: storey e. Brain Res. 2012 Aug 30;1471:138-54. doi: 10.1016/j.brainres.2012.06.035. Epub 2012 Jul 3. Brain Res. 2012. PMID: 22771856
Spinocerebellar ataxia type 20.
Storey E, Knight MA, Forrest SM, Gardner RJ. Storey E, et al. Cerebellum. 2005;4(1):55-7. doi: 10.1080/14734220410019048. Cerebellum. 2005. PMID: 15895561
391 results