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Publications by Eun-Kee Bae
Fixation-Off Sensitivity in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Switching From Traditional Sodium Channel Blockers to Lacosamide in Patients With Epilepsy
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Related publications
Anesthetic Considerations in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome: A Case Series
Canadian Journal of Anaesthesia
Medicine
Anesthesiology
Pain Medicine
Sigmoid Volvulus in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS): A Rare Occurrence
BMJ Case Reports
Medicine
Mutation in the Mitochondrial tRNAVal Causes Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes
Mitochondrion
Molecular Medicine
Cell Biology
Molecular Biology
Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes: A Unique Late Onset Presentation and Subsequent Management on a Symptomatic Basis
American Medical Student Research Journal
Wolff-Parkinson-White Syndrome in a Patient With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Mimicking Juvenile Myoclonic Epilepsy
Journal of Clinical Neurology (Korea
Neurology
Gastro-Intestinal Involvement in M.3243A>G-Associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes
Internal Medicine
Internal Medicine
Medicine
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
Frontiers in Neurology
Neurology
Taurine Ameliorates Impaired the Mitochondrial Function and Prevents Stroke-Like Episodes in Patients With MELAS
Internal Medicine
Internal Medicine
Medicine
Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population
American Journal of Human Genetics
Genetics
