Focal and Generalized Seizures May Occur in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes (MELAS) Patients
Author:
Affiliation:
1. Krankenanstalt Rudolfstiftung, Vienna, Austria
2. Laboratory of Biochemistry, UR “Human Nutrition and Metabolic Disorders” Faculty of Medicine, Monastir, Tunisie
Publisher
SAGE Publications
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Link
http://journals.sagepub.com/doi/pdf/10.1177/0883073814567539
Reference19 articles.
1. Phenotypic Analysis of Epilepsy in the Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes–Associated Mitochondrial DNA A3243G Mutation
2. Adult-onset of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome Presenting as Acute Meningoencephalitis: A Case Report
3. Infantile Presentation of the mtDNA A3243G tRNALeu (UUR) Mutation
4. The expanding clinical phenotype of the tRNALeu(UUR) A→G mutation at np 3243 of mitochondrial DNA: Diabetic embryopathy associated with mitochondrial cytopathy
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1. Epilepsy and MELAS syndrome: literature review and clinical observation;Epilepsy and paroxysmal conditions;2023-12-22
2. Epilepsy in mitochondrial diseases. Clinical lecture;Russian Journal of Child Neurology;2023-05-18
3. Clinical features of epileptic seizures in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes;Seizure;2023-03
4. MELAS;Diagnostic Imaging: Pädiatrische Neuroradiologie;2023
5. Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes;Life;2021-10-20
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