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Morphologic features of hypermetabolic mitochondrial disease. A light microscopic, histochemical and electron microscopic study.

作者信息

Afifi A K, Ibrahim M Z, Bergman R A, Haydar N A, Mire J, Bahuth N, Kaylani F

出版信息

J Neurol Sci. 1972 Mar;15(3):271-90. doi: 10.1016/0022-510x(72)90070-6.

DOI:10.1016/0022-510x(72)90070-6
PMID:5014093
Abstract
摘要

相似文献

1
Morphologic features of hypermetabolic mitochondrial disease. A light microscopic, histochemical and electron microscopic study.
J Neurol Sci. 1972 Mar;15(3):271-90. doi: 10.1016/0022-510x(72)90070-6.
2
Severe hypermetabolism with primary abnormality of skeletal muscle mitochondria.伴有骨骼肌线粒体原发性异常的严重高代谢
Ann Intern Med. 1971 Apr;74(4):548-58. doi: 10.7326/0003-4819-74-4-548.
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A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy.电子显微镜在检测杜氏型肌营养不良症携带者中的潜在作用。
J Neurol Neurosurg Psychiatry. 1973 Aug;36(4):643-50. doi: 10.1136/jnnp.36.4.643.
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Acromegaly: histochemical and electron microscopic changes in deltoid and intercostal muscle.肢端肥大症：三角肌和肋间肌的组织化学及电子显微镜下的变化
Neurology. 1974 Jun;24(6):589-93. doi: 10.1212/wnl.24.6.589.
5
Familial "mitochondrial" myopathy. A myopathy associated with disordered oxidative metabolism in muscle fibres. 1. Clinical, electrophysiological and pathological findings.家族性“线粒体”肌病。一种与肌纤维氧化代谢紊乱相关的肌病。1. 临床、电生理及病理表现。
J Neurol Sci. 1972 Jul;16(3):343-70. doi: 10.1016/0022-510x(72)90197-9.
6
Some observations on the etiology of the fulminant hyperthermia-stress syndrome.关于暴发性高热-应激综合征病因的一些观察
Perspect Biol Med. 1976 Autumn;20(1):120-30. doi: 10.1353/pbm.1976.0061.
7
Experimental ischemic myopathy.
J Neurol Sci. 1974 Sep;23(1):129-61. doi: 10.1016/0022-510x(74)90148-8.
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Rod (nemaline) bodies in the skeletal muscle of an acute schizophrenic patient.
Neurology. 1973 Jul;23(7):769-80. doi: 10.1212/wnl.23.7.769.
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[Histological, histocytochemical and electron microscope studies on myotonic dystrophy].
No To Shinkei. 1968 Apr;20(4):337-48.
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[Electron microscopic studies on the skeletal muscles in progressive muscular dystrophy. 2. (with special reference to preclinical stages and carriers)].
Nihon Seikeigeka Gakkai Zasshi. 1970 Jul;44(7):493-502.

引用本文的文献

1
Megamitochondria formation - physiology and pathology.巨型线粒体的形成——生理学与病理学
J Cell Mol Med. 2002 Oct-Dec;6(4):497-538. doi: 10.1111/j.1582-4934.2002.tb00452.x.
2
Thyrotoxic myopathy. Pathomorphological observations of human material and experimentally induced thyrotoxicosis in rats.甲状腺毒症性肌病。人体材料及大鼠实验性甲状腺毒症的病理形态学观察。
Acta Neuropathol. 1981;53(3):237-48. doi: 10.1007/BF00688027.
3
The histochemical characterization of the coupling state of skeletal muscle mitochondria.骨骼肌线粒体偶联状态的组织化学特征
Histochemistry. 1980;69(3):217-32. doi: 10.1007/BF00489769.
4
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.
5
A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophy.电子显微镜在检测杜氏型肌营养不良症携带者中的潜在作用。
J Neurol Neurosurg Psychiatry. 1973 Aug;36(4):643-50. doi: 10.1136/jnnp.36.4.643.
6
[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.
7
[Sudanophilic (mitochondria) myopathy (author's transl)].嗜苏丹性（线粒体）肌病（作者译）
Z Neurol. 1974 Apr 4;206(4):309-26.
8
The biochemical basis of mitochondrial diseases.线粒体疾病的生化基础。
J Bioenerg Biomembr. 1988 Apr;20(2):161-91. doi: 10.1007/BF00768393.
9
Alteration in skeletal muscle mitochondria of cold-acclimated rats: association with enhanced metabolic response to noradrenaline.冷适应大鼠骨骼肌线粒体的改变：与去甲肾上腺素增强的代谢反应相关。
J Bioenerg Biomembr. 1977 Feb;9(1):41-63. doi: 10.1007/BF00745042.
10
Skeletal muscle pathology in chronic heart block.慢性心脏传导阻滞中的骨骼肌病理学
J Clin Pathol. 1977 May;30(5):467-72. doi: 10.1136/jcp.30.5.467.