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进行性肌阵挛癫痫患者的尿糖胺聚糖

Urinary glycosaminoglycans in patients with progressive myoclonus epilepsy.

作者信息

Federico A, D'Auria N

出版信息

J Neurol. 1979 Jan 5;220(4):291-5. doi: 10.1007/BF00314153.

DOI:10.1007/BF00314153
PMID:90138
Abstract

Urinary GAGs analysis in Progressive Myoclonus Epilepsy (PME) showed an accumulation of uronic acid in the fraction eluted by 1 M NaCl and 3 M NaCl. As analogous changes were found in other myoclonic and epileptic patients receiving large doses of anticonvulsant drugs, these alterations in the GAG urinary pattern were not considered a primary disturbance of PME.

摘要

进行性肌阵挛癫痫(PME)患者的尿糖胺聚糖(GAGs)分析显示,在被1 M氯化钠和3 M氯化钠洗脱的组分中存在糖醛酸积累。由于在接受大剂量抗惊厥药物治疗的其他肌阵挛和癫痫患者中也发现了类似变化,因此GAG尿模式的这些改变不被认为是PME的原发性紊乱。

相似文献

1
Urinary glycosaminoglycans in patients with progressive myoclonus epilepsy.进行性肌阵挛癫痫患者的尿糖胺聚糖
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2
Content and composition of urinary glycosaminoglycans in the patients with myoclonus epilepsy with and without Lafora bodies.伴有和不伴有Lafora小体的肌阵挛性癫痫患者尿糖胺聚糖的含量及组成
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本文引用的文献

1
Progressive myoclonus epilepsy without Lafora bodies.无Lafora小体的进行性肌阵挛癫痫
J Neurol Neurosurg Psychiatry. 1969 Apr;32(2):116-22. doi: 10.1136/jnnp.32.2.116.
2
Lafora's disease. An ultrastructural and histochemical study.
Acta Neuropathol. 1974;30(3):189-96. doi: 10.1007/BF00688920.
3
Mycolonus epilepsy with cherry-red spot in adult: a peculiar form of mucopolysaccharidosis. (A clinical genetic, chemical and ultrastructural study).成人伴有樱桃红斑的肌阵挛癫痫:一种特殊形式的黏多糖贮积症。(一项临床遗传学、化学及超微结构研究)
Acta Neurol (Napoli). 1973 Sep-Oct;28(5):542-9.
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Studies in myoclonus epilepsy (Lafora body form). I. Isolation and preliminary characterization of Lafora bodies in two cases.肌阵挛性癫痫(拉福拉小体形式)的研究。I. 两例拉福拉小体的分离及初步特征分析。
Arch Neurol. 1968 Jul;19(1):15-33. doi: 10.1001/archneur.1968.00480010033002.
5
Muscle in Lafora disease.拉福拉病中的肌肉。
Arch Neurol. 1974 Dec;31(6):396-406. doi: 10.1001/archneur.1974.00490420062007.
6
Myoclonus epilepsy with cerebellar Lafora bodies. Report of a case.伴有小脑拉福拉小体的肌阵挛性癫痫。病例报告。
J Neurol Neurosurg Psychiatry. 1976 Apr;39(4):357-61. doi: 10.1136/jnnp.39.4.357.
7
Findings in routine laboratory examination in progressive myoclonus epilepsy.进行性肌阵挛癫痫的常规实验室检查结果。
Acta Neurol Scand. 1975 Jan;51(1):12-20. doi: 10.1111/j.1600-0404.1975.tb01355.x.
8
Content and composition of urinary glycosaminoglycans in the patients with myoclonus epilepsy with and without Lafora bodies.伴有和不伴有Lafora小体的肌阵挛性癫痫患者尿糖胺聚糖的含量及组成
Acta Neurol Scand. 1977 Oct;56(4):291-8. doi: 10.1111/j.1600-0404.1977.tb01436.x.
9
Changes of brain glyco-conjugates in Unverricht-Lundborg's disease.翁韦里希特-伦德伯格病中脑糖缀合物的变化。
Acta Neurol (Napoli). 1978 Jan-Feb;33(1):58-62.
10
The excretion patterns of urinary glucosaminoglycans in a family with progressive familial myoclonus epilepsy.一个进行性家族性肌阵挛癫痫家族中尿糖胺聚糖的排泄模式。
Acta Neurol Scand. 1975 Sep;52(3):216-30. doi: 10.1111/j.1600-0404.1975.tb05776.x.