Apply the Hirano or Japanese criteria when diagnosing MELAS.
作者信息
Finsterer Josef, Mehri Sounira
机构信息
Neurology & Neurophysiology Center, Vienna, Austria.
Biochemistry Laboratory, LR12ES05 "Nutrition-Functional Foods and Vascular Health", Faculty of Medicine, Monastir, Tunisia.
出版信息
Ann Med Surg (Lond). 2022 Nov 17;84:104965. doi: 10.1016/j.amsu.2022.104965. eCollection 2022 Dec.
Abstract
摘要
相似文献
1
Apply the Hirano or Japanese criteria when diagnosing MELAS.诊断线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）时应用平野或日本标准。
Ann Med Surg (Lond). 2022 Nov 17;84:104965. doi: 10.1016/j.amsu.2022.104965. eCollection 2022 Dec.
2
Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).线粒体肌病、脑病、乳酸酸中毒和卒中样发作（MELAS）的单肌纤维分析
Ann Neurol. 1994 Apr;35(4):413-9. doi: 10.1002/ana.410350407.
3
Patients with MELAS with negative myopathology for characteristic ragged-red fibers.肌肉病理检查未见特征性破碎红纤维的 MELAS 患者。
J Neurol Sci. 2020 Jan 15;408:116499. doi: 10.1016/j.jns.2019.116499. Epub 2019 Oct 15.
4
Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).血管中线粒体DNA增加以及线粒体肌病、脑病、乳酸性酸中毒和卒中样发作（MELAS）中的破碎红纤维。
Ann Neurol. 1993 Mar;33(3):275-80. doi: 10.1002/ana.410330308.
5
MELAS syndrome with rare manifestations misdiagnosed as vasculitis in the absence of lactic acidosis: A case report.无乳酸酸中毒表现罕见的线粒体脑肌病伴乳酸血症和卒中样发作综合征被误诊为血管炎：一例报告
Ann Med Surg (Lond). 2022 Aug 27;81:104483. doi: 10.1016/j.amsu.2022.104483. eCollection 2022 Sep.
6
When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?何时应诊断为线粒体肌病、脑病、乳酸酸中毒和卒中样发作（MELAS）？
Arq Neuropsiquiatr. 2015 Nov;73(11):959-67. doi: 10.1590/0004-282X20150154.
7
A comment on a case report about perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode.关于一例伴有类中风发作的神经元核内包涵体病灌注异常病例报告的评论
Cereb Circ Cogn Behav. 2023 Jan 30;4:100160. doi: 10.1016/j.cccb.2023.100160. eCollection 2023.
8
Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes.线粒体肌病、脑病、乳酸酸中毒和卒中样发作中的线粒体DNA突变与肌肉病理改变
Muscle Nerve Suppl. 1995;3:S113-8. doi: 10.1002/mus.880181423.
9
[Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].[线粒体脑肌病、乳酸酸中毒和卒中样发作/肌阵挛性癫痫伴破碎红纤维/由线粒体DNA 8344A>G突变引起的 Leigh重叠综合征]
Beijing Da Xue Xue Bao Yi Xue Ban. 2020 Oct 18;52(5):851-855. doi: 10.19723/j.issn.1671-167X.2020.05.009.
10
Acute hearing loss in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).一名患有线粒体肌病、脑病、乳酸性酸中毒和卒中样发作（MELAS）的患者出现急性听力丧失。
Acta Neurol Taiwan. 2007 Sep;16(3):168-72.
本文引用的文献
1
MELAS syndrome with rare manifestations misdiagnosed as vasculitis in the absence of lactic acidosis: A case report.无乳酸酸中毒表现罕见的线粒体脑肌病伴乳酸血症和卒中样发作综合征被误诊为血管炎：一例报告
Ann Med Surg (Lond). 2022 Aug 27;81:104483. doi: 10.1016/j.amsu.2022.104483. eCollection 2022 Sep.
2
Metabolic stroke or stroke-like lesion: Peculiarities of a phenomenon.代谢性卒中或类卒中病变：一种现象的特点
J Neurol Sci. 2020 May 15;412:116726. doi: 10.1016/j.jns.2020.116726. Epub 2020 Feb 7.
3
Renal involvement in MELAS syndrome - a series of 5 cases and review of the literature.线粒体脑肌病伴乳酸血症和卒中样发作综合征的肾脏受累——5例病例系列及文献复习
Clin Nephrol. 2013 Dec;80(6):456-63. doi: 10.5414/CN107063.
4
MELAS: a nationwide prospective cohort study of 96 patients in Japan.线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）：日本一项针对96例患者的全国性前瞻性队列研究。
Biochim Biophys Acta. 2012 May;1820(5):619-24. doi: 10.1016/j.bbagen.2011.03.015. Epub 2011 Apr 2.
5
Melas: an original case and clinical criteria for diagnosis.线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）：1例原始病例及诊断临床标准
Neuromuscul Disord. 1992;2(2):125-35. doi: 10.1016/0960-8966(92)90045-8.
Zotero 插件