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- W40332308 abstract "The sporadic degenerative ataxias and the autosomal dominantly inherited spinocerebellar ataxias (SCAs) are adult-onset progressive diseases in which ataxia is the prominent clinical manifestation. In most of these diseases, ataxia is the consequence of degeneration of the cerebellar cortex and its fiber connections. Patients with sporadic degenerative ataxias can be subdivided into patients with multiple system atrophy which is associated with widespread degeneration in the central nervous system and patients with a more benign clinical syndrome, named sporadic adult-onset ataxia of unknown etiology (SAOA). While the sporadic degenerative ataxias are diseases of unknown etiology, the SCAs are caused by dominant mutations of single genes." @default.
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- W40332308 date "2009-01-01" @default.
- W40332308 modified "2023-09-23" @default.
- W40332308 title "Sporadic Degenerative Ataxias and the Dominantly Inherited Spinocerebellar Ataxias" @default.
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- W40332308 doi "https://doi.org/10.1016/b978-008045046-9.00612-4" @default.
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