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引用本文的文献

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Follow-up of neurophysiological tests and CT in late-onset cerebellar ataxia and multiple system atrophy.迟发性小脑共济失调和多系统萎缩的神经生理学检查及CT随访
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CT in autosomal dominant and idiopathic cerebellar ataxia.常染色体显性遗传性和特发性小脑共济失调的CT表现
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Multiple system atrophy presenting as parkinsonism: clinical features and diagnostic criteria.表现为帕金森综合征的多系统萎缩:临床特征与诊断标准
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Electromyography and nerve conduction study in autosomal dominant olivopontocerebellar atrophy.常染色体显性遗传性橄榄体脑桥小脑萎缩的肌电图与神经传导研究
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Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophy.患有隐性橄榄体脑桥小脑萎缩的双胞胎中的肌腺苷酸脱氨酶缺乏症。
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橄榄体脑桥小脑变性的计算机断层扫描

Computed tomography of olivopontocerebellar degeneration.

作者信息

Savoiardo M, Bracchi M, Passerini A, Visciani A, Di Donato S, Cocchini F

出版信息

AJNR Am J Neuroradiol. 1983 May-Jun;4(3):509-12.

PMID:6410784
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8334901/
Abstract

Computed tomographic (CT) studies of 17 cases of olivopontocerebellar degeneration are reported. In all cases, atrophy of brainstem and cerebellum was found. Atrophy of the cerebellar hemispheres was equal to, or more marked than, atrophy of the vermis. Dilatation of lateral ventricles and cerebral sulci was often present. These findings, which are in agreement with the pathologic data, are compared with those reported in other cerebellar atrophic processes. Knowledge of the distribution of the atrophic changes is essential in attempting a differential diagnosis among the degenerative diseases involving the posterior fossa nervous structures.

摘要

报告了17例橄榄体脑桥小脑萎缩的计算机断层扫描(CT)研究。所有病例均发现脑干和小脑萎缩。小脑半球萎缩程度与蚓部萎缩相当或更明显。常出现侧脑室和脑沟增宽。这些与病理数据相符的发现与其他小脑萎缩性病变的报告结果进行了比较。了解萎缩性改变的分布对于鉴别涉及后颅窝神经结构的退行性疾病至关重要。