| 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 | Long-term outcomes of ketogenic diet in patients with tuberous sclerosis complex-derived epilepsy | EPILEPSY RESEARCH |
| 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 | 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 |
| 2018 | Efficacy of Stiripentol in Dravet Syndrome with or without SCN1A Mutations
| JOURNAL OF CLINICAL NEUROLOGY |
| 2017 | 얼굴마비로 방문하여 높은 delta neutrophil index를 보였고 골수 외 침윤을 동반한 급성골수세포백혈병으로 진단된 4세 여자 환자
| Pediatric Emergency Medicine Journal |
| 2017 | Mowat-Wilson syndrome presenting with fever-associated seizures | EPILEPTIC DISORDERS |
| 2017 | Effect of ketogenic diet and other dietary therapies on anti-epileptic drug concentrations in patients with epilepsy | JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS |
| 2017 | Low glycemic index treatment in patients with drug-resistant epilepsy | BRAIN & DEVELOPMENT |
| 2017 | 국소 겉질 형성이상으로 인한 소아 뇌전증 환자에서 뇌전증 수술 후 항경련제 복용 중단
| Journal of the Korean Child Neurology Society |
| 2017 | KCNT1 돌연변이가 확인된 영아 이동성 부분 발작뇌전증 환아에서의 Quinidine 치료를 시도한 영아 1예
| Journal of the Korean Child Neurology Society |
| 2017 | 드라베 증후군의 SCN1A 유전자 변이 양상 | Journal of the Korean Child Neurology Society |
| 2017 | Efficacy of Treatment for Infantile Spasms: A systematic review | CLINICAL NEUROPHARMACOLOGY |
| 2016 | 미토콘드리아 호흡연쇄 복합체 결함이 동반된 난치성 소아 뇌전증에서의 Zonisamide 부가 요법 | Journal of the Korean Child Neurology Society |
| 2015 | Ictal ontogeny in Dravet syndrome | CLINICAL NEUROPHYSIOLOGY |
| 2015 | A practical, simple, and useful method of categorizing interictal EEG features in children | NEUROLOGY |
| 2014 | A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorder | BRAIN & DEVELOPMENT |
| 2013 | Short-term efficacy and tolerability of rufinamide adjunctive therapy in children with refractory generalised epilepsy
| EPILEPTIC DISORDERS |
| 2012 | Long-term effectiveness of ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy | BRAIN & DEVELOPMENT |
| 2012 | Subclinical hypothyroidism during valproic acid therapy in children and adolescents with epilepsy | NEUROPEDIATRICS |
| 2010 | 방사선 검사에서 뇌병변이 확인된 미숙아에서의 대근육 운동발달의 예후 인자
| Journal of the Korean Child Neurology Society |
| 2010 | A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation
| Korean Journal of Pediatrics |
| 2010 | Ischemic stroke in a 7-month-old infant with antiphospholipid antibody and homozygous C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism | JOURNAL OF CHILD NEUROLOGY |
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