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Commentary: Point Prevalence and Associated Factors of Hip Displacement in Pediatric Patients With Mitochondrial Disease.

作者信息

Finsterer Josef

机构信息

Neurology & Neurophysiology Center, Vienna, Austria.

出版信息

Front Pediatr. 2022 Jun 21;10:894611. doi: 10.3389/fped.2022.894611. eCollection 2022.

DOI:10.3389/fped.2022.894611
PMID:35799698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9254360/
Abstract
摘要

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本文引用的文献

1
Case Report: A Case of β-Ureidopropionase Deficiency Complicated With MELAS Syndrome Caused by Variant and Mitochondrial Gene Variant.病例报告：一例由变异体和线粒体基因变异导致的β-脲基丙酸酶缺乏症合并线粒体脑肌病伴乳酸酸中毒及卒中样发作综合征
Front Pediatr. 2022 Feb 21;10:838341. doi: 10.3389/fped.2022.838341. eCollection 2022.
2
Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implications.线粒体 DNA A3243G 变异相关的视网膜病变：当前的观点和临床意义。
Surv Ophthalmol. 2021 Sep-Oct;66(5):838-855. doi: 10.1016/j.survophthal.2021.02.008. Epub 2021 Feb 18.
3
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.
4
Focal Segmental Glomerulosclerosis Associated with Chronic Progressive External Ophthalmoplegia and Mitochondrial DNA A3243G Mutation.局灶节段性肾小球硬化症与慢性进行性眼外肌麻痹及线粒体DNA A3243G突变相关。
Nephron. 2018;138(3):243-248. doi: 10.1159/000485109. Epub 2017 Nov 30.
5
[Unexceptional symptoms as expression of MELAS].[无特异性症状作为线粒体脑肌病伴乳酸血症和卒中样发作（MELAS）的表现]
Ned Tijdschr Geneeskd. 2010;154:A2168.