Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Syndrome (MELAS)
Overview
Authors
Affiliations
Protective Effect of Mitochondrial ND2 C5178A Gene Mutation on Cell and Mitochondrial Functions.
Tian L, Zhu C, Yang H, Li Y, Liu Y Oxid Med Cell Longev. 2021; 2021:4728714.
PMID: 34336093 PMC: 8315857. DOI: 10.1155/2021/4728714.
Metabolic stroke in a patient with bi-allelic OPA1 mutations.
Zerem A, Yosovich K, Rappaport Y, Libzon S, Blumkin L, Ben-Sira L Metab Brain Dis. 2019; 34(4):1043-1048.
PMID: 30972688 DOI: 10.1007/s11011-019-00415-2.
Ganetzky R, Falk M Mol Genet Metab. 2018; 123(3):301-308.
PMID: 29428506 PMC: 5849405. DOI: 10.1016/j.ymgme.2018.01.010.
Magnetic resonance imaging in MELAS syndrome.
Rosen L, Phillips S, Enzmann D Neuroradiology. 1990; 32(2):168-71.
PMID: 2398945 DOI: 10.1007/BF00588572.