MELAS syndrome.
作者信息
Koga S J, Hodges M, Markin C, Gorman P
机构信息
Department of Medical Education, Providence Medical Center, Portland, USA.
出版信息
West J Med. 1995 Oct;163(4):379-81.
Abstract
摘要
相似文献
1
MELAS syndrome.线粒体脑肌病伴乳酸血症和卒中样发作综合征
West J Med. 1995 Oct;163(4):379-81.
2
[Cardiological manifestation of MELAS syndrome associated with mDNA mutation at position 3234].
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3
MELAS syndrome, diabetes and thyroid disease: the role of mitochondrial oxidative stress.
Clin Endocrinol (Oxf). 2009 Feb;70(2):340-1. doi: 10.1111/j.1365-2265.2008.03341.x. Epub 2008 Jul 7.
4
Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation.一名患有MELAS和线粒体DNA T14487C突变的患者出现迟发性线粒体疾病。
Chin Med J (Engl). 2019 Mar 20;132(6):716-718. doi: 10.1097/CM9.0000000000000139.
5
[MELAS syndrome associated with Klinefelter syndrome].[与克兰费尔特综合征相关的线粒体脑肌病伴乳酸血症和卒中样发作综合征]
Nihon Rinsho. 2002 Apr;60 Suppl 4:625-8.
6
[MELAS syndrome masquerading as herpes encephalitis: genetic diagnosis].[伪装成疱疹性脑炎的线粒体脑肌病伴乳酸血症和卒中样发作综合征：基因诊断]
Rev Neurol. 2001;33(2):148-50.
7
Population prevalence of the MELAS A3243G mutation.MELAS A3243G突变的人群患病率。
Mitochondrion. 2007 May;7(3):230-3. doi: 10.1016/j.mito.2006.12.004. Epub 2007 Jan 8.
8
Mitochondrial A3243G mutation with manifestation of acute dilated cardiomyopathy.线粒体A3243G突变伴急性扩张型心肌病表现
Circ Heart Fail. 2012 Jan;5(1):e1-3. doi: 10.1161/CIRCHEARTFAILURE.111.963900.
9
[MELAS-Leigh superposition syndrome: a case report].
Zhonghua Nei Ke Za Zhi. 2020 Feb 1;59(2):140-143. doi: 10.3760/cma.j.issn.0578-1426.2020.02.009.
10
Mortality, disability, and intensive care in patients with mitochondrial 3243A>G mutation.
Intensive Care Med. 2015 Aug;41(8):1493-5. doi: 10.1007/s00134-015-3879-x. Epub 2015 Jun 3.
引用本文的文献
1
Acute Management of Neurological Events in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome: A Case Report.线粒体脑肌病伴乳酸酸中毒及卒中样发作（MELAS）综合征神经事件的急性处理：一例报告
Cureus. 2025 May 12;17(5):e83959. doi: 10.7759/cureus.83959. eCollection 2025 May.
2
Long-Term Safety of Systemic Ozone Therapy in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS).线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）患者全身臭氧治疗的长期安全性
Cureus. 2023 Nov 4;15(11):e48261. doi: 10.7759/cureus.48261. eCollection 2023 Nov.
3
A Young Child with Recurrent Episodes of Headaches and Vision Loss: Diagnostic Clues?一名反复出现头痛和视力丧失症状的幼儿：诊断线索？
J Pediatr Neurosci. 2021 Jan-Mar;16(1):82-84. doi: 10.4103/jpn.JPN_91_20. Epub 2021 Jun 25.
4
MELAS syndrome associated with a new mitochondrial tRNA-Val gene mutation (m.1616A>G).与新的线粒体tRNA-Val基因突变（m.1616A>G）相关的线粒体脑肌病伴乳酸酸中毒及卒中样发作综合征
BMJ Case Rep. 2017 Sep 11;2017:bcr-2017-220934. doi: 10.1136/bcr-2017-220934.
本文引用的文献
1
2
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.糖尿病是tRNALeu（UUR）基因中线粒体DNA点突变的异质表型特征之一。
FEBS Lett. 1993 Apr 26;321(2-3):194-6. doi: 10.1016/0014-5793(93)80106-5.
3
The syndrome of mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes presenting without stroke.线粒体脑肌病、乳酸酸中毒及卒中样发作综合征（无卒中表现）
Arch Neurol. 1993 Mar;50(3):275-8. doi: 10.1001/archneur.1993.00540030041012.
4
A molecular basis for human hypersensitivity to aminoglycoside antibiotics.人类对氨基糖苷类抗生素超敏反应的分子基础。
Nucleic Acids Res. 1993 Sep 11;21(18):4174-9. doi: 10.1093/nar/21.18.4174.
5
Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.一名散发性氨基糖苷类耳毒性患者的线粒体核糖体RNA基因突变
Am J Otolaryngol. 1993 Nov-Dec;14(6):399-403. doi: 10.1016/0196-0709(93)90113-l.
6
Inborn errors of metabolism: a new purview of internal medicine.先天性代谢缺陷：内科医学的一个新领域。
Ann Intern Med. 1994 Feb 1;120(3):245-6. doi: 10.7326/0003-4819-120-3-199402010-00013.
7
A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA.一种与线粒体DNA突变相关的糖尿病亚型。
N Engl J Med. 1994 Apr 7;330(14):962-8. doi: 10.1056/NEJM199404073301403.
8
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.与抗生素诱导性和非综合征性耳聋相关的线粒体核糖体RNA突变
Nat Genet. 1993 Jul;4(3):289-94. doi: 10.1038/ng0793-289.
9
Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.伴有破碎红纤维（线粒体异常）的肌阵挛性癫痫：疾病实体还是综合征？两例病例的光镜和电镜研究及文献复习
J Neurol Sci. 1980 Jul;47(1):117-33. doi: 10.1016/0022-510x(80)90031-3.
10
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.
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