Correlation of Serum Biomarkers and Magnetic Resonance Spectroscopy in Monitoring Disease Progression in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Due to mtDNA A3243G Mutation
Author:
Publisher
Frontiers Media SA
Subject
Neurology (clinical),Neurology
Reference22 articles.
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3. Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis;Debray;Clin Chem.,2007
4. Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers;Weiduschat;Neurology,2014
5. Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures;Mager;Eur J Paediatr Neurol.,2011
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3. Mitochondrial Cardiomyopathy: The Roles of mt-tRNA Mutations;Journal of Clinical Medicine;2022-10-30
4. Consider a cerebellar stroke-like lesion only after adequately ruling out all differential diagnoses;Acta Neurologica Belgica;2022-07-26
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