Ataxia and autonomic dysfunction as presenting symptoms in late-onset Alexander disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Reference9 articles.
1. PROGRESSIVE FIBRINOID DEGENERATION OF FIBRILLARY ASTROCYTES ASSOCIATED WITH MENTAL RETARDATION IN A HYDROCEPHALIC INFANT
2. αB-crystallin is expressed in non-lenticular tissues and accumulates in Alexander's disease brain
3. Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease
4. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease
5. Unusual variants of Alexander's disease
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. A case of adult onset of Alexander disease with nocturnal painless burns, autonomic dysfunction, and peripheral nerve impairment;Clinical Neurology and Neurosurgery;2021-01
2. Parkinsonism phenotype in a family with adult onset Alexander disease and a novel mutation of GFAP;Clinical Neurology and Neurosurgery;2020-08
3. A Novel Mutation in the Adult-Onset Alexander’s Disease GFAP Gene;Case Reports in Medicine;2019-01-10
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