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Spinocerebellar ataxia type 11 in the Chinese Han population
Neurological Sciences, 10/07/09

Xu Q et al. – To investigate the frequency of SCA11 in Chinese SCA patients, the authors examined the TTBK2 gene in 68 unrelated probands diagnosed with dominantly inherited ataxia using the denaturing high–performance liquid chromatography method. All analyzed samples displayed the normal elution profile, which denoted that no disease–related mutation was identified. They provided the evidence that SCA11 is a rare form of ataxia in China.

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Physiologic Alterations in Ataxia
Archives of Neurology, 10/19/09 Relevance Score: 90%

Antioxidants and other pharmacological treatments for Friedreich ataxia
Cochrane Reviews, 10/09/09 Relevance Score: 89%

Extracerebellar MRI—Lesions in Ataxia Telangiectasia Go Along with Deficiency of the GH/IGF-1 Axis, Markedly Reduced Body Weight, High Ataxia Scores and Advanced Age
The Cerebellum, 11/12/09 Relevance Score: 88%

Isolated ataxia after pure left insular cortex infarction
Neurological Sciences, 10/20/09 Relevance Score: 88%

Cellular and Molecular Pathways Triggering Neurodegeneration in the Spinocerebellar Ataxias
The Cerebellum, 11/12/09 Relevance Score: 87%