Multiple system atrophies
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference58 articles.
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1. SPG11mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration;American Journal of Medical Genetics Part B: Neuropsychiatric Genetics;2009-10-05
2. Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter;Neuropathology;2005-12
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4. References;Metabolic and Degenerative Diseases of the Central Nervous System;1995
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