Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: an important cause of stroke in young people-Reference-Cited by-同舟云学术

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Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: an important cause of stroke in young people

Published:2012-02-10 Issue:1040 Volume:88 Page:326-334
ISSN:0032-5473
Container-title:Postgraduate Medical Journal
language:en
Short-container-title:Postgrad Med J

Author:

Goodfellow John Aaron,Dani Krishna,Stewart Willie,Santosh Celestine,McLean John,Mulhern Sharon,Razvi Saif

Publisher

BMJ

Subject

General Medicine

Cited by 49 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Adult-onset mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A case report and review of its conventional and diffusion- weighted MRI features;Neurology Asia;2024-06

2. Mitochondrial ataxia - Unravelling the puzzle;Annals of Movement Disorders;2024-05

3. Elderly onset of MELAS carried an M.3243A >G mutation in a female with deafness and visual deficits: A case report;Clinical Case Reports;2024-03

4. Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with mitochondrial DNA 3243A>G mutation masquerading as autoimmune encephalitis: A case report;World Journal of Clinical Cases;2023-05-16

5. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: a case report from Nepal;Annals of Medicine & Surgery;2023-05-03

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