| 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 | 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 | 조기영아성간질성뇌병증 환자에서 de novo로 확인된 HCN1 유전자 돌연변이 1예 보고
| Laboratory Medicine Online |
| 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 | The Vestibuloplasty Using Non-eugenol based Non-zinc Oxide Oral Dressing Material | Journal of Korean Dental Science |
| 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 | Clinical characteristics of KCNQ2 encephalopathy | BRAIN & DEVELOPMENT |
| 2021 | Corrigendum to 'Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy' [Brain Dev. 42(6) (2020) 438-448] | BRAIN & DEVELOPMENT |
| 2021 | Screening of Tuberous Sclerosis-Associated Neuropsychiatric Disorders in Korea Using the TAND Checklist
| Annals of Child Neurology |
| 2020 | Cannabidiol for Treating Lennox-Gastaut Syndrome and Dravet Syndrome in Korea
| JOURNAL OF KOREAN MEDICAL SCIENCE |
| 2020 | Epilepsy surgery for pediatric patients with mild malformation of cortical development | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
| 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 | Factors associated with seizure and cognitive outcomes after epilepsy surgery for low-grade epilepsy-associated neuroepithelial tumors in children
| Clinical and Experimental Pediatrics |
| 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 | Treatment Response to Acquired Aphasia with Seizures and Prognosis through Electroencephalogram on Cognitive Function
| Annals of Child Neurology |
| 2019 | Clinical features and treatment efficacy in cdkl5 mutation-related epileptic encephalopathy in the infant
| Annals of Child Neurology |
| 2019 | Predicting the Outcome of Critically Ill Children and Adolescents with Electroencephalography
| Annals of Child Neurology |
| 2019 | Precise detection of low-level somatic mutation in resected epilepsy brain tissue | ACTA NEUROPATHOLOGICA |
| 2019 | Genetic and clinical features of SCN8A developmental and epileptic encephalopathy | EPILEPSY RESEARCH |
| 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 | Epilepsy Surgery for Children With Low-Grade Epilepsy-Associated Tumors: Factors Associated With Seizure Recurrence and Cognitive Function | PEDIATRIC NEUROLOGY |
| 2018 | 미토콘드리아 질환에서 웨스트 증후군 환자의 경련 발생 연령에 따른 임상 양상 비교
| Journal of the Korean Child Neurology Society |
| 2018 | Rufinamide efficacy and safety in children aged 1-4 years with Lennox-Gastaut syndrome | BRAIN & DEVELOPMENT |
| 2018 | Diagnostic exome sequencing을 통한 KBG 증후군의 조기 진단
| Journal of the Korean Child Neurology Society |
| 2018 | Long-term Outcome of Resective Epilepsy Surgery in Patients With Lennox-Gastaut Syndrome | PEDIATRICS |
| 2018 | Interregional metabolic connectivity of 2-deoxy-2[18 F]fluoro-D-glucose positron emission tomography in vagus nerve stimulation for pediatric patients with epilepsy: A retrospective cross-sectional study | EPILEPSIA |
| 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 | Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patients | BRAIN & DEVELOPMENT |
| 2018 | Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy | EPILEPSY RESEARCH |
| 2018 | Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing
| BMC MEDICAL GENOMICS |
| 2018 | Efficacy of Stiripentol in Dravet Syndrome with or without SCN1A Mutations
| JOURNAL OF CLINICAL NEUROLOGY |
| 2017 | Mowat-Wilson syndrome presenting with fever-associated seizures | EPILEPTIC DISORDERS |
| 2017 | Low glycemic index treatment in patients with drug-resistant epilepsy | BRAIN & DEVELOPMENT |
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