Cargando…

Clinical characteristics and surgical outcomes in children with mild malformation of cortical development and oligodendroglial hyperplasia in epilepsy

OBJECTIVE: Mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) is a new and rare histopathological entity of cortical developmental malformations. The clinical characteristics of MOGHE remain challenging. METHODS: Children with histologically confirmed MOG...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Xianyu, Zhu, Ying, Liu, Qingzhu, Zhang, Shuang, Wu, Pengxia, Sun, Yu, Zhang, Jie, Wang, Ruofan, Ji, Taoyun, Wang, Shuang, Liu, Xiaoyan, Jiang, Yuwu, Cai, Lixin, Wu, Ye
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2023
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472402/ https://www.ncbi.nlm.nih.gov/pubmed/37144544 http://dx.doi.org/10.1002/epi4.12755

Ejemplares similares

Seizure Outcome and Its Prognostic Predictors After Hemispherotomy in Children With Refractory Epilepsy in a Chinese Pediatric Epileptic Center
por: Ji, Taoyun, et al.
Publicado: (2019)

Epileptic Patient with Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia and Epilepsy (MOGHE): A Case Report and Review of the Literature
por: Verentzioti, A., et al.
Publicado: (2019)

Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
por: Bonduelle, Thomas, et al.
Publicado: (2021)

Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis
por: Liu, Qingzhu, et al.
Publicado: (2023)

Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II
por: Zhang, Zhongbin, et al.
Publicado: (2018)

Post-Operative Seizure Freedom Need not be Elusive in Mild Oligodendroglial Hyperplasia and Epilepsy (MOGHE)
por: Chatterjee, Aparajita, et al.
Publicado: (2021)

Safety and efficacy of rapid withdrawal of antiseizure medications during long‐term video‐electroencephalogram monitoring in children with drug‐resistant epilepsy: A retrospective study
por: Wang, Shuang, et al.
Publicado: (2023)

Vagus nerve stimulation in children with drug-resistant epilepsy of monogenic etiology
por: Xie, Han, et al.
Publicado: (2022)

A prediction model integrating synchronization biomarkers and clinical features to identify responders to vagus nerve stimulation among pediatric patients with drug‐resistant epilepsy
por: Ma, Jiayi, et al.
Publicado: (2022)

Seizure features and outcomes in 50 children with GATOR1 variants: A retrospective study, more favorable for epilepsy surgery
por: Wang, Hao, et al.
Publicado: (2023)

Brain Somatic Variant in Ras-Like Small GTPase RALA Causes Focal Cortical Dysplasia Type II
por: Xu, Han, et al.
Publicado: (2022)

Malformations of cortical development and epilepsy
por: Leventer, Richard J., et al.
Publicado: ( 200)

High-throughput, automated quantification of white matter neurons in mild malformation of cortical development in epilepsy
por: Liu, Joan YW, et al.
Publicado: (2014)

Lesional Intractable Epileptic Spasms in Children: Electroclinical Localization and Postoperative Outcomes
por: Wang, Shuang, et al.
Publicado: (2022)

Brain functional connectivity‐based prediction of vagus nerve stimulation efficacy in pediatric pharmacoresistant epilepsy
por: Chen, Hao, et al.
Publicado: (2023)

Mild malformations of cortical development in sleep‐related hypermotor epilepsy due to KCNT1 mutations
por: Rubboli, Guido, et al.
Publicado: (2018)

Long‐term seizure outcome after epilepsy surgery in patients with mild malformation of cortical development and focal cortical dysplasia
por: Veersema, Tim J., et al.
Publicado: (2018)

Why Malformations of Cortical Development Cause Epilepsy
por: Represa, Alfonso
Publicado: (2019)

Neurodevelopmental Findings and Epilepsy in Malformations of Cortical Development
por: Şah, Olcay, et al.
Publicado: (2021)

Language Dominance in Patients With Malformations of Cortical Development and Epilepsy
por: Kuchukhidze, Giorgi, et al.
Publicado: (2019)

Efficacy of Anti-seizure Medications, Quinidine, and Ketogenic Diet Therapy for KCNT1-Related Epilepsy and Genotype-Efficacy Correlation Analysis
por: Lin, Zehong, et al.
Publicado: (2022)

Midbrain–hindbrain malformations in patients with malformations of cortical development and epilepsy: A series of 220 patients
por: Kuchukhidze, Giorgi, et al.
Publicado: (2013)

A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II
por: Shepherd, Caterina, et al.
Publicado: (2013)

Effects of Stable Vagus Nerve Stimulation Efficacy on Autistic Behaviors in Ten Pediatric Patients With Drug Resistant Epilepsy: An Observational Study
por: Wang, Zhiyan, et al.
Publicado: (2022)

Bilateral oligodendroglial hamartomas: A rare cause of drug-resistant epilepsy in a pediatric patient
por: Munjal, Havisha, et al.
Publicado: (2022)

Oligodendroglial glycolytic stress triggers inflammasome activation and neuropathology in Alzheimer’s disease
por: Zhang, Xinwen, et al.
Publicado: (2020)

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities
por: Zhang, Yujia, et al.
Publicado: (2015)

Genetic markers in oligodendroglial tumours
por: Velnar, Tomaz, et al.
Publicado: (2010)

Gene Expression in Oligodendroglial Tumors
por: Shaw, Elisabeth J., et al.
Publicado: (2010)

Oligodendroglial pathology in canine distemper
por: Zurbriggen, A., et al.
Publicado: (1997)

Oligodendroglial Heterogeneity in Neuropsychiatric Disease
por: Bøstrand, Sunniva M. K., et al.
Publicado: (2021)

Dicer Deletion in Astrocytes Inhibits Oligodendroglial Differentiation and Myelination
por: Liu, Kun, et al.
Publicado: (2021)

Impaired oligodendroglial turnover is associated with myelin pathology in focal cortical dysplasia and tuberous sclerosis complex
por: Scholl, Theresa, et al.
Publicado: (2017)

Metabolic phenotyping of hand automatisms in mesial temporal lobe epilepsy
por: Mo, Jiajie, et al.
Publicado: (2022)

The National Comprehensive Governance for epilepsy prevention and control in China
por: Li, Shichuo, et al.
Publicado: (2021)

Response to antiseizure medications in epileptic patients with malformation of cortical development
por: Chen, Wei, et al.
Publicado: (2021)

Altered capicua transcriptional repressor gene expression exhibits distinct prognostic value for isocitrate dehydrogenase-mutant oligodendroglial tumors
por: Han, Fuxin, et al.
Publicado: (2018)

Variants in LAMC3 Causes Occipital Cortical Malformation
por: Qian, Xiaohang, et al.
Publicado: (2021)

Vagus nerve stimulation for pediatric patients with intractable epilepsy between 3 and 6 years of age: study protocol for a double-blind, randomized control trial
por: Ji, Taoyun, et al.
Publicado: (2019)

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis
por: Yang, Xiaoling, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_c605iu2rpce4i4vspc6du23s47