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Radiomic Models for Diagnosing Juvenile Myoclonic Epilepsy Should Note Its Genetic Heterogeneity

  • Josef Finsterer (Neurology & Neurophysiology Center)
  • 투고 : 2022.12.11
  • 심사 : 2022.12.19
  • 발행 : 2023.02.01

초록

키워드

참고문헌

  1. Kim KM, Hwang H, Sohn B, Park K, Han K, Ahn SS, et al. Development and validation of MRI-based radiomics models for diagnosing juvenile myoclonic epilepsy. Korean J Radiol 2022;23:1281-1289
  2. Amrutkar C, Riel-Romero RM. Juvenile myoclonic epilepsy. [Updated 2022 Aug 8]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan [cited 2022 Dec 11]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK537109/
  3. Berrechid AG, Bendjebara M, Bouteiller D, Nasri A, Peuvion JN, Marie Y, et al. Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg disease. Epileptic Disord 2019;21:359-365
  4. Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia 2018;59:1011-1019