2023 | Long-term efficacy and safety of adjunctive perampanel in pediatric patients aged 4-19 years with epilepsy: a real-world study
| SCIENTIFIC REPORTS |
2023 | Electroencephalography characteristics related to risk of sudden unexpected death in epilepsy in patients with Dravet syndrome
| FRONTIERS IN NEUROLOGY |
2023 | Letter on: 3D figure of epilepsy syndromes
| EPILEPSIA OPEN |
2023 | Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders | JOURNAL OF MOLECULAR DIAGNOSTICS |
2023 | Genotypes and phenotypes of DNM1 encephalopathy | JOURNAL OF MEDICAL GENETICS |
2023 | Efficacy and Safety of Lamotrigine Adjunctive Therapy in Lennox-Gastaut Syndrome
| Annals of Child Neurology |
2023 | A decrease in the incidence of encephalitis in South Korea during the COVID‐19 pandemic: A nationwide study between 2010 and 2021 | JOURNAL OF MEDICAL VIROLOGY |
2022 | Analysis of trio test in neurodevelopmental disorders
| FRONTIERS IN PEDIATRICS |
2022 | Effects of the ketogenic diet therapy in patients with STXBP1-related encephalopathy | EPILEPSY RESEARCH |
2022 | Clinical Spectrum and Treatment Outcomes of Patients with Developmental and/or Epileptic Encephalopathy with Spike-and-Wave Activation in Sleep
| Annals of Child Neurology |
2022 | Effects of Cannabidiol on Adaptive Behavior and Quality of Life in Pediatric Patients With Treatment-Resistant Epilepsy
| JOURNAL OF CLINICAL NEUROLOGY |
2022 | Association of hypercalciuria with vitamin D supplementation in patients undergoing ketogenic dietary therapy
| FRONTIERS IN NUTRITION |
2022 | Epilepsy with SLC35A2 Brain Somatic Mutations in Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE)
| Annals of Child Neurology |
2022 | Epidural grid, a new methodology of invasive intracranial EEG monitoring: A technical note and experience of a single center | EPILEPSY RESEARCH |
2022 | Efficacy of the Ketogenic Diet for Pediatric Epilepsy According to the Presence of Detectable Somatic mTOR Pathway Mutations in the Brain
| JOURNAL OF CLINICAL NEUROLOGY |
2022 | Efficacy and prognosis of long-term, high-dose steroid therapy for Lennox-Gastaut syndrome | EPILEPSY RESEARCH |
2021 | Robot-Assisted Stereoelectroencephalography for Pediatric Epilepsy Surgery: The First Case in Korea
| Annals of Child Neurology |
2021 | Disparate treatment outcomes according to presence of pathogenic mutations in West syndrome | EPILEPSIA |
2021 | Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish | HUMAN MOLECULAR GENETICS |
2021 | Clinical Features and Treatment Outcomes of Seronegative Pediatric Autoimmune Encephalitis
| JOURNAL OF CLINICAL NEUROLOGY |
2021 | Comparative Proteome Research in a Zebrafish Model for Vanishing White Matter Disease
| INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES |
2021 | Clinical characteristics of KCNQ2 encephalopathy | BRAIN & DEVELOPMENT |
2021 | Effects of Salbutamol in Collagen like Tail Subunit of Asymmetric Acetylcholinesterase-Related Congenital Myasthenic Syndrome: A First Korean Case
| Annals of Child Neurology |
2020 | Cannabidiol for Treating Lennox-Gastaut Syndrome and Dravet Syndrome in Korea
| JOURNAL OF KOREAN MEDICAL SCIENCE |
2020 | Hybrid Machine Learning Scheme for Classification of BECTS and TLE Patients Using EEG Brain Signals
| IEEE ACCESS |
2020 | The phenotype and treatment of SCN2A-related developmental and epileptic encephalopathy | EPILEPTIC DISORDERS |
2020 | Long-term outcomes of ketogenic diet in patients with tuberous sclerosis complex-derived epilepsy | EPILEPSY RESEARCH |
2020 | Efficacy and Safety of Lacosamide in Adolescents with Lennox-Gastaut Syndrome
| Annals of Child Neurology |
2020 | Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern | EPILEPSY RESEARCH |
2020 | Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy | BRAIN & DEVELOPMENT |
2020 | Reanalysis of Genomic Sequencing Results in a Clinical Laboratory: Advantages and Limitations
| FRONTIERS IN NEUROLOGY |
2020 | Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development | PEDIATRIC NEUROLOGY |
2019 | Prognostic Factors for Absence Epilepsy in Childhood
| Annals of Child Neurology |
2019 | Predicting the Outcome of Critically Ill Children and Adolescents with Electroencephalography
| Annals of Child Neurology |
2019 | Genetic and clinical features of SCN8A developmental and epileptic encephalopathy | EPILEPSY RESEARCH |
2019 | The ketogenic diet in children 3 years of age or younger: a 10-year single-center experience
| SCIENTIFIC REPORTS |
2019 | Proband-Only Clinical Exome Sequencing for Neurodevelopmental Disabilities | PEDIATRIC NEUROLOGY |
2019 | Optimized Treatment for Infantile Spasms: Vigabatrin versus Prednisolone versus Combination Therapy
| Journal of Clinical Medicine |
2019 | Short- and long-term seizure-free outcomes of dietary treatment in infants according to etiology | Seizure - European Journal of Epilepsy |
2019 | Clobazam as an adjunctive treatment for infantile 넴는 | Epilepsy & Behavior |
2019 | A Child With Lymphangioma Due to Somatic Mutation in PIK3CA Successfully Treated With Everolimus | PEDIATRIC NEUROLOGY |
2019 | Epilepsy Surgery for Children With Low-Grade Epilepsy-Associated Tumors: Factors Associated With Seizure Recurrence and Cognitive Function | PEDIATRIC NEUROLOGY |
2018 | 신경질환에서 정맥주사용 면역글로불린 치료의 임상적 이용
| Journal of the Korean Child Neurology Society |
2018 | Diagnostic exome sequencing을 통한 KBG 증후군의 조기 진단
| Journal of the Korean Child Neurology Society |
2018 | Vigabatrin and high-dose prednisolone therapy for patients with West syndrome | EPILEPSY RESEARCH |
2018 | The efficacy of ketogenic diet for specific genetic mutation in developmental and epileptic encephalopathy
| FRONTIERS IN NEUROLOGY |
2018 | Adverse Events During Perampanel Adjunctive Therapy in Intractable Epilepsy
| JOURNAL OF CLINICAL NEUROLOGY |
2018 | Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy | EPILEPSY RESEARCH |
2018 | Severe peri-ictal respiratory dysfunction is common in Dravet syndrome.
| JOURNAL OF CLINICAL INVESTIGATION |
2018 | Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing
| BMC MEDICAL GENOMICS |