Research Evidence
Peer-reviewed studies linked via MeSH term "Mitochondrial Encephalomyopathies" from the MEDLINE/PubMed database.
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Novel TARS2 variant identified in a Chinese patient with mitochondrial encephalomyopathy and a systematic review.
[object Object], [object Object], [object Object] et al. · Am J Med Genet A · 2023
PMID: 36218002Meta-Analysis
l-Arginine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes: A Systematic Review.
[object Object], [object Object], [object Object] et al. · Neurology · 2022
Evaluation of long-term treatment of children with congenital lactic acidosis with dichloroacetate.
[object Object], [object Object], [object Object] et al. · Pediatrics · 2008
Mitochondrial encephalomyopathy.
[object Object], [object Object] · Handb Clin Neurol · 2023
PMID: 37562887Review
Succinyl-CoA Synthetase Dysfunction as a Mechanism of Mitochondrial Encephalomyopathy: More than Just an Oxidative Energy Deficit.
[object Object], [object Object] · Int J Mol Sci · 2023
Ocular manifestations of mitochondrial neurogastrointestinal encephalomyopathy: A case report and literature review.
[object Object], [object Object], [object Object] et al. · Am J Med Genet A · 2023
PMID: 37530213Review
Genetic aberration analysis of mitochondrial respiratory complex I implications in the development of neurological disorders and their clinical significance.
[object Object], [object Object], [object Object] et al. · Ageing Res Rev · 2023
PMID: 36905963Review
Stem cell-derived mitochondria transplantation: A promising therapy for mitochondrial encephalomyopathy.
[object Object], [object Object], [object Object] et al. · CNS Neurosci Ther · 2021
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Position paper on diagnosis, prognosis, and treatment by the MNGIE International Network.
[object Object], [object Object], [object Object] et al. · J Inherit Metab Dis · 2021
Cardiac complications in inherited mitochondrial diseases.
[object Object], [object Object], [object Object] et al. · Heart Fail Rev · 2021
PMID: 32728985Review
Search all PubMed articles for Mitochondrial encephalomyopathy
Research data from MEDLINE/PubMed
Related Conditions
Mitochondrial neurogastrointestinal encephalomyopathy syndrome(child)
Severe X-linked mitochondrial encephalomyopathy(child)
Hearing loss, encephaloneuropathy, obesity, valvulopathy syndrome(child)
Mitochondrial DNA depletion syndrome encephalomyopathic form(child)
Myoclonic epilepsy with ragged red fibers(child)
FAST kinase domains 2-related infantile mitochondrial encephalomyopathy(child)
Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome(child)
Encephalopathy(parent)
Mitochondrial myopathy(parent)
Quick Facts
- SNOMED CT
- 447292006
- UMLS CUI
- C0162666
- Fully Specified Name
- Mitochondrial encephalomyopathy (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.