多核肌病——一例与肌纤维“多核”变性相关的先天性非进行性肌病 - Suppr | 超能文献

[Multicore myopathy--a case of congenital non-progressive myopathy associated with "multicore" degeneration of muscle fibers].

作者信息

Tanimura R, Suzuki Y, Segawa M, Fukuyama Y

出版信息

Rinsho Shinkeigaku. 1974 Jul 1;14(7):613-22.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

[Multicore myopathy--a case of congenital non-progressive myopathy associated with "multicore" degeneration of muscle fibers].多核肌病——一例与肌纤维“多核”变性相关的先天性非进行性肌病

Rinsho Shinkeigaku. 1974 Jul 1;14(7):613-22.

2

[Centronuclear (myotubular) myopathy: a case report].[中央核（肌管）性肌病：一例报告]

Rev Hosp Clin Fac Med Sao Paulo. 1992 Sep-Oct;47(5):237-9.

3

Multicore disease. A recently recognized congenital myopathy associated with multifocal degeneration of muscle fibers.多核病。一种最近被认识到的先天性肌病，与肌纤维的多灶性变性相关。

Mayo Clin Proc. 1971 Oct;46(10):666-81.

4

Congenital non-progressive myopathy, associated with scoliosis--clinical, histological, histochemical and electron microscopic studies of seven cases.

Nihon Seikeigeka Gakkai Zasshi. 1980 Apr;54(4):381-402.

5

Quantitative histopathology in congenital myopathies.先天性肌病的定量组织病理学

Riv Neurol. 1987 Jul-Aug;57(4):261-8.

6

Congenital myopathies with "diagnostic" pathological features.具有“诊断性”病理特征的先天性肌病

J Med. 1987;18(2):93-107.

7

[Multicore disease].[多核疾病]

Rinsho Shinkeigaku. 1973 Apr;13(4):221-7.

8

A novel congenital myopathy with apoptotic changes.一种伴有凋亡改变的新型先天性肌病。

Ann Neurol. 2000 Apr;47(4):531-6.

9

[Congenital non-progressive myopathy with central axis (central core disease)].[伴有中央轴索的先天性非进行性肌病（中央核心病）]

Arch Fr Pediatr. 1971 Jan;28(1):65-82.

10

[Congenital myopathies. 9 case reports and general review].

Union Med Can. 1980 Feb;109(2):256-76.

引用本文的文献

1

Minicore myopathy.

Klin Wochenschr. 1982 Nov 2;60(21):1351-5. doi: 10.1007/BF01716214.

2

Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter.中央轴空病：父女肌肉活检组织化学及超微结构研究

J Neurol. 1978 Apr 14;218(1):55-62. doi: 10.1007/BF00314719.