-related Mitochondrial Disorder with MNGIE- and Leigh-like Features.
作者信息
Finsterer Josef
机构信息
Krankenanstalt Rudolfstiftung, Messerli Institute, Vienna, Austria.
出版信息
Ann Indian Acad Neurol. 2020 May-Jun;23(3):365-366. doi: 10.4103/aian.AIAN_438_19. Epub 2020 Jun 10.
Abstract
摘要
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本文引用的文献
1
Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalomyopathy-Like Syndrome with Polymerase-Gamma Mutations.伴有聚合酶γ突变的线粒体神经胃肠性脑肌病样综合征中的白质脑病
Ann Indian Acad Neurol. 2019 Jul-Sep;22(3):325-327. doi: 10.4103/aian.AIAN_34_18.
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Glucocorticoids for mitochondrial disorders.用于线粒体疾病的糖皮质激素。
Singapore Med J. 2015 Feb;56(2):122-3. doi: 10.11622/smedj.2015026.
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[Familial progressive external opthalmoplegia, parkinsonism and polyneuropathy associated with POLG1 mutation].[与POLG1突变相关的家族性进行性眼外肌麻痹、帕金森病和多发性神经病]
Rinsho Shinkeigaku. 2014;54(5):417-22. doi: 10.5692/clinicalneurol.54.417.
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The role of brain MRI in mitochondrial neurogastrointestinal encephalomyopathy.脑磁共振成像在线粒体神经胃肠性脑肌病中的作用
Neuroradiol J. 2013 Oct;26(5):520-30. doi: 10.1177/197140091302600505. Epub 2013 Nov 7.
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Mitochondrial depletion syndromes in children and adults.儿童和成人的线粒体耗竭综合征。
Can J Neurol Sci. 2013 Sep;40(5):635-44. doi: 10.1017/s0317167100014852.
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Parieto-occipital lobe epilepsy caused by a POLG1 compound heterozygous A467T/W748S genotype.由 POLG1 复合杂合 A467T/W748S 基因型引起的顶枕叶癫痫。
Epilepsy Behav. 2011 Jun;21(2):206-10. doi: 10.1016/j.yebeh.2011.03.003. Epub 2011 Apr 22.
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