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Fatal cerebral hemorrhage in mitochondrial encephalomyopathy. Clinical and pathological data of a case.

作者信息

Kato Haruhisa, Uchigata Masanobu, Iijima Mutsumi, Shimizu Seiichiro, Nonaka Ikuya, Goto Yuichi

出版信息

J Neurol. 2006 Apr;253(4):529-30. doi: 10.1007/s00415-005-0010-1. Epub 2005 Nov 14.

DOI:10.1007/s00415-005-0010-1
PMID:16283102
Abstract
摘要

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2
[Mitochondrial myopathy and mitochondrial encephalomyopathy].[线粒体肌病和线粒体脑病]
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引用本文的文献

1
Cerebral imaging in paediatric mitochondrial disorders.小儿线粒体疾病的脑部成像
Neuroradiol J. 2018 Dec;31(6):596-608. doi: 10.1177/1971400918786054. Epub 2018 Jul 6.
2
Causes of Death in Adults with Mitochondrial Disease.线粒体疾病成年患者的死因
JIMD Rep. 2016;26:103-13. doi: 10.1007/8904_2015_449. Epub 2015 Sep 10.
3
Spontaneous intracerebral hemorrhage in CADASIL.CADASIL 相关性颅内出血。

本文引用的文献

1
Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.在MELAS/MERFF表型中发现一种新的线粒体DNA突变（G12147A）。
Arch Neurol. 2004 Feb;61(2):269-72. doi: 10.1001/archneur.61.2.269.
2
Recurrent brain hematomas in MELAS associated with an ND5 gene mitochondrial mutation.与ND5基因线粒体突变相关的线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）中的复发性脑血肿。
Neurology. 2000 Jul 25;55(2):317-8. doi: 10.1212/wnl.55.2.317.
3
The T-C(8356) mitochondrial DNA mutation in a Japanese family.一个日裔家族中的T-C(8356)线粒体DNA突变
J Headache Pain. 2013 Dec 17;14(1):98. doi: 10.1186/1129-2377-14-98.
4
Cerebellar hematoma in a carrier of the A3243G MELAS mutation.携带A3243G MELAS突变者的小脑血肿。
Neurol Sci. 2011 Apr;32(2):365-6. doi: 10.1007/s10072-011-0493-8. Epub 2011 Feb 16.
J Neurol. 1996 Jun;243(6):441-4. doi: 10.1007/BF00900496.
4
A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.一种与线粒体DNA赖氨酸转运RNA基因新的点突变相关的肌阵挛性癫痫伴破碎红纤维/线粒体脑肌病伴乳酸血症和卒中样发作重叠综合征
Eur J Hum Genet. 1993;1(1):80-7. doi: 10.1159/000472390.
5
Mitochondrial encephalomyopathies: CT and MRI findings and correlations with clinical features.线粒体脑肌病：CT和MRI表现及其与临床特征的相关性
Eur Neurol. 1995;35(4):199-205. doi: 10.1159/000117128.
6
Progression from MERRF to MELAS phenotype in a patient with combined respiratory complex I and IV deficiencies.
J Neurol Sci. 1988 Dec;88(1-3):327-37. doi: 10.1016/0022-510x(88)90229-8.