Suppr超能文献

[先天性肌病的临床特征与鉴别诊断]

[Clinical characteristics and differential diagnosis of congenital myopathies].

作者信息

Saĭkova L A, Lobzin V S

出版信息

Zh Nevropatol Psikhiatr Im S S Korsakova. 1988;88(3):3-6.

PMID:3381610
Abstract

Sixteen patients with congenital myopathies with the onset of the disease in early childhood were examined. All patients were subjected to morphological investigation of biopsy samples of muscle tissue, using histochemical methods for the determination of the activity of redox and glycolysis enzymes. A clinical polymorphism of these forms of myodystrophies and the presence of nondifferentiated variants were established. The distribution of the activities of oxidation and glycolysis enzymes was histochemically different.

摘要

对16例在幼儿期发病的先天性肌病患者进行了检查。所有患者均对肌肉组织活检样本进行了形态学研究,采用组织化学方法测定氧化还原酶和糖酵解酶的活性。确定了这些形式的肌营养不良症的临床多态性以及未分化变体的存在。氧化酶和糖酵解酶活性的分布在组织化学上有所不同。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验