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Ultrastructural features of intracellular lipid in normal human muscle.

作者信息

Prineas J, Ng R C

出版信息

Neurology. 1967 Nov;17(11):1092-8. doi: 10.1212/wnl.17.11.1092.

DOI:10.1212/wnl.17.11.1092
PMID:4167616
Abstract
摘要

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引用本文的文献

1
Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.伴有细胞色素c氧化酶和肉碱缺乏的致死性脂质贮积性肌病。对长期冷冻肌肉中细胞色素c氧化酶的细胞化学-精细结构联合鉴定的贡献。
Virchows Arch A Pathol Anat Histopathol. 1983;399(1):11-23. doi: 10.1007/BF00666215.
2
Ultrastructural study of globular inclusions in human skeletal muscle mitochondria.人类骨骼肌线粒体中球状包涵体的超微结构研究
Acta Neuropathol. 1980;52(1):35-40. doi: 10.1007/BF00687226.
3
[Ultrastructural changes of muscle fibers in progressive muscular dystrophy of Duchenne type].
[杜兴氏型进行性肌营养不良中肌纤维的超微结构变化]
Acta Neuropathol. 1971;18(2):173-89. doi: 10.1007/BF00687605.
4
[Mitochondrial anomalies with peculiar distribution in a muscular dystrophy with pelvic onset (author's transl)].
Acta Neuropathol. 1974;30(4):295-303. doi: 10.1007/BF00697012.
5
Morphological features in a neutral lipid storage disease.一种中性脂质贮积病的形态学特征。
J Clin Pathol. 1975 Sep;28(9):701-10. doi: 10.1136/jcp.28.9.701.