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Huntington's chorea. Deficiency of gamma-aminobutyric acid in brain.

作者信息

Perry T L, Hansen S, Kloster M

出版信息

N Engl J Med. 1973 Feb 15;288(7):337-42. doi: 10.1056/NEJM197302152880703.

DOI:10.1056/NEJM197302152880703
PMID:4345566
Abstract
摘要

相似文献

1
Huntington's chorea. Deficiency of gamma-aminobutyric acid in brain.亨廷顿舞蹈病。大脑中γ-氨基丁酸缺乏。
N Engl J Med. 1973 Feb 15;288(7):337-42. doi: 10.1056/NEJM197302152880703.
2
Evidence for descending pallido-nigral GABA-containing neurons.下行含γ-氨基丁酸的苍白球-黑质神经元的证据。
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3
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Choline acetylase and glutamic acid decarboxylase in Huntington's chorea. A preliminary study.亨廷顿舞蹈病中的胆碱乙酰化酶和谷氨酸脱羧酶。一项初步研究。
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5
[The role of dopamine in the physiology and pathology of the basal ganglia].[多巴胺在基底神经节生理和病理中的作用]
Zh Nevropatol Psikhiatr Im S S Korsakova. 1972;72(4):595-603.
6
Application of principles of steady-state kinetics to the estimation of gamma-aminobutyric acid turnover rate in nuclei of rat brain.稳态动力学原理在大鼠脑细胞核中γ-氨基丁酸周转率估算中的应用。
J Pharmacol Exp Ther. 1977 Feb;200(2):277-84.
7
Cannabinoid (CB(1)), GABA(A) and GABA(B) receptor subunit changes in the globus pallidus in Huntington's disease.亨廷顿舞蹈病患者苍白球中大麻素(CB(1))、γ-氨基丁酸A(GABA(A))和γ-氨基丁酸B(GABA(B))受体亚基的变化
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Reduced glutamic-acid-decarboxylase activity of post-mortem brain in Huntington's chorea.亨廷顿舞蹈病患者死后大脑中谷氨酸脱羧酶活性降低。
Lancet. 1973 May 19;1(7812):1090-2. doi: 10.1016/s0140-6736(73)90398-x.
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Brain dopamine and the syndromes of Parkinson and Huntington. Clinical, morphological and neurochemical correlations.脑多巴胺与帕金森综合征和亨廷顿综合征。临床、形态学及神经化学相关性
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Huntington's chorea. Post-mortem measurement of glutamic acid decarboxylase, choline acetyltransferase and dopamine in basal ganglia.亨廷顿舞蹈症。基底神经节中谷氨酸脱羧酶、胆碱乙酰转移酶和多巴胺的尸检测量
Brain. 1974 Sep;97(3):457-72. doi: 10.1093/brain/97.1.457.

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亨廷顿舞蹈病中阳离子-氯离子协同转运体功能障碍导致纹状体氯离子调节异常及γ-氨基丁酸能信号受损
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Nervenarzt. 2022 Feb;93(2):179-190. doi: 10.1007/s00115-021-01224-8. Epub 2021 Nov 11.
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Insights into GABAergic system alteration in Huntington's disease.对亨廷顿病中 GABA 能系统改变的深入了解。
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Huntington's disease: the coming of age.亨廷顿舞蹈症:走向成熟
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