伴有线粒体脑肌病、乳酸酸中毒和卒中样发作综合征（MELAS）的波动型磁共振成像 - Suppr

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超能文献

Fluctuating MR images with mitochondrial encephalopathy, lactic acidosis, stroke-like syndrome (MELAS).

作者信息

Abe K, Inui T, Hirono N, Mezaki T, Kobayashi Y, Kameyama M

机构信息

Department of Neurology, Sumitoma Hospital, Osaka.

出版信息

Neuroradiology. 1990;32(1):77. doi: 10.1007/BF00593950.

DOI:10.1007/BF00593950

PMID:2333140

Abstract

摘要

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Fluctuating MR images with mitochondrial encephalopathy, lactic acidosis, stroke-like syndrome (MELAS).伴有线粒体脑肌病、乳酸酸中毒和卒中样发作综合征（MELAS）的波动型磁共振成像

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Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes.基于从无任何肌病改变的活检肌肉中提取的线粒体DNA全序列诊断的成人起病的线粒体肌病、脑病、乳酸性酸中毒和卒中样脑病（MELAS）样脑病

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引用本文的文献

Comparison of conventional and diffusion-weighted MRI and proton MR spectroscopy in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like events.线粒体脑肌病、乳酸酸中毒和卒中样发作患者的常规MRI、扩散加权MRI及质子磁共振波谱分析比较

Neuroradiology. 2004 Feb;46(2):113-7. doi: 10.1007/s00234-003-1138-2. Epub 2003 Dec 12.

Mitochondrial encephalomyopathy: comparison of conventional MR imaging with diffusion-weighted and diffusion tensor imaging: case report.线粒体脑肌病：传统磁共振成像与扩散加权成像及扩散张量成像的比较：病例报告

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Reversible cortical oedema mimicking cortical dysplasia in mitochondrial disorder.线粒体疾病中类似皮质发育异常的可逆性皮质水肿

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本文引用的文献

Mitochondrial encephalomyopathy with lactate-pyruvate elevation and brain infarctions.

Neurology. 1984 Jan;34(1):72-7. doi: 10.1212/wnl.34.1.72.

Mitochondrial encephalomyopathy: fluctuating symptoms and CT.

Neurology. 1984 Nov;34(11):1456-60. doi: 10.1212/wnl.34.11.1456.

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.线粒体肌病、脑病、乳酸酸中毒和卒中样发作：一种独特的临床综合征。

Ann Neurol. 1984 Oct;16(4):481-8. doi: 10.1002/ana.410160409.

Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism.线粒体脑肌病：一组氧化代谢存在缺陷的神经肌肉疾病。

Isr J Med Sci. 1977 Feb;13(2):161-4.

Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia.

Arch Neurol. 1977 Mar;34(3):180-5. doi: 10.1001/archneur.1977.00500150066013.

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