遗传性共济失调：对五例有共同祖先病例的病理学研究。 - Suppr

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超能文献

Hereditary ataxia: a pathologic study of five cases of common ancestry.

作者信息

SCHUT J W, HAYMAKER W

出版信息

J Neuropathol Clin Neurol. 1951 Jul;1(3):183-213.

PMID:24541014

Abstract

摘要

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Hereditary ataxia: a pathologic study of five cases of common ancestry.遗传性共济失调：对五例有共同祖先病例的病理学研究。

J Neuropathol Clin Neurol. 1951 Jul;1(3):183-213.

Hereditary ataxia; a survey of certain clinical, pathologic and genetic features with linkage data on five additional hereditary factors.遗传性共济失调；对某些临床、病理和遗传特征以及五个额外遗传因素的连锁数据的调查。

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Hereditary primary lateral sclerosis and progressive nonfluent aphasia.遗传性原发性侧索硬化伴进行性非流利性失语。

J Neurol. 2019 May;266(5):1079-1090. doi: 10.1007/s00415-019-09235-x. Epub 2019 Mar 5.

The Genetic Basis of the Hereditary Ataxias.遗传性共济失调的遗传基础。

J R Coll Physicians Lond. 1969 Oct;4(1):88-92.

Reduction of protein kinase A-mediated phosphorylation of ATXN1-S776 in Purkinje cells delays onset of Ataxia in a SCA1 mouse model.蛋白激酶 A 介导的 ATXN1-S776 磷酸化减少可延迟 SCA1 小鼠模型中小脑浦肯野细胞的发病。

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[The problem of combined systematrophies of the central nervous system].

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The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis.CAG/聚谷氨酰胺重复序列疾病：基因产物与分子发病机制

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Clinical aspects of CAG repeat diseases.CAG重复序列疾病的临床方面。

Brain Pathol. 1997 Jul;7(3):881-900. doi: 10.1111/j.1750-3639.1997.tb00892.x.

Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype.由1型脊髓小脑共济失调（SCA-1）突变引起的橄榄体脑桥小脑萎缩的结构和免疫细胞化学特征定义了一种独特的表型。

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Linkage between late onset, dominant spinocerebellar ataxia and HLA.迟发性显性脊髓小脑共济失调与人类白细胞抗原之间的连锁关系。

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Regression of cerebellar syndrome with long-term administration of 5-HTP or the combination 5-HTP-benserazide.长期服用5-羟色氨酸（5-HTP）或5-羟色氨酸与苄丝肼的组合后小脑综合征的消退。

Ital J Neurol Sci. 1984 Sep;5(3):253-66. doi: 10.1007/BF02043955.

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