Radiomic Models for Diagnosing Juvenile Myoclonic Epilepsy Should Note Its Genetic Heterogeneity.
作者信息
Finsterer Josef
机构信息
Neurology & Neurophysiology Center, Vienna, Austria.
出版信息
Korean J Radiol. 2023 Feb;24(2):166-167. doi: 10.3348/kjr.2022.0982.
Abstract
摘要
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引用本文的文献
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Response to "Radiomic Models for Diagnosing Juvenile Myoclonic Epilepsy Should Note Its Genetic Heterogeneity".对《用于诊断青少年肌阵挛癫痫的放射组学模型应注意其遗传异质性》的回应
Korean J Radiol. 2023 Feb;24(2):168-169. doi: 10.3348/kjr.2022.1000.
本文引用的文献
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Development and Validation of MRI-Based Radiomics Models for Diagnosing Juvenile Myoclonic Epilepsy.基于 MRI 的放射组学模型在青少年肌阵挛性癫痫诊断中的开发与验证。
Korean J Radiol. 2022 Dec;23(12):1281-1289. doi: 10.3348/kjr.2022.0539.
2
Juvenile myoclonic epilepsy phenotype in a family with Unverricht-Lundborg disease.家族性 Unverricht-Lundborg 病中少年肌阵挛性癫痫表型。
Epileptic Disord. 2019 Aug 1;21(4):359-365. doi: 10.1684/epd.2019.1078.
3
DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians.BRD2 启动子的 DNA 甲基化与白种人中的青少年肌阵挛性癫痫有关。
Epilepsia. 2018 May;59(5):1011-1019. doi: 10.1111/epi.14058. Epub 2018 Apr 2.
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