| 2012 | An Arg528His Mutation of the CACNL1A3 Gene in a Korean Family with Hypokalemic Periodic Paralysis
| Journal of the Korean Child Neurology Society |
| 2012 | Genetic and epileptic features in Rett syndrome
| YONSEI MEDICAL JOURNAL |
| 2012 | A multicenter trial of oxcarbazepine oral suspension monotherapy in children newly diagnosed with partial seizures: a clinical and cognitive evaluation | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
| 2012 | Rufinamide as an adjuvant treatment in children with Lennox-Gastaut syndrome | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
| 2012 | Early cardiac evaluation in children with non-specific mitochondrial disease with isolated mitochondrial respiratory chain complex I defect | JOURNAL OF PAEDIATRICS AND CHILD HEALTH |
| 2012 | Efficacy of VeinViewer in pediatric peripheral intravenous access: a randomized controlled trial | EUROPEAN JOURNAL OF PEDIATRICS |
| 2012 | Mitochondria DNA polymorphisms are associated with susceptibility to endometriosis | DNA AND CELL BIOLOGY |
| 2012 | Effects of lamotrigine on cognition and behavior compared to carbamazepine as monotherapy for children with partial epilepsy | BRAIN & DEVELOPMENT |
| 2012 | Various indications for a modified Atkins diet in intractable childhood epilepsy | BRAIN & DEVELOPMENT |
| 2012 | Effects of cytochrome P450 (CYP)2C19 polymorphisms on pharmacokinetics of phenobarbital in neonates and infants with seizures | ARCHIVES OF DISEASE IN CHILDHOOD |
| 2011 | A1 Segment Hypoplasia/aplasia Detected by Magnetic Resonance Angiography in Neuropediatric Patients
| Journal of the Korean Child Neurology Society |
| 2011 | A Case of Early Onset MELAS Patient with Wolff-Parkinson-White Syndrome
| Journal of the Korean Child Neurology Society |
| 2011 | A Case of Metachromatic Leukodystrophy Confirmed by Molecular Genetic Analysis
| Journal of the Korean Child Neurology Society |
| 2011 | Comparative trial of low- and high-dose zonisamide as monotherapy for childhood epilepsy | SEIZURE-EUROPEAN JOURNAL OF EPILEPSY |
| 2010 | Leigh 증후군 환아에서의 안과적 이상 소견
| Korean Journal of Pediatrics |
| 2010 | Risk factors of ocular involvement in children with mitochondrial respiratory chain complex defect
| Korean Journal of Pediatrics |
| 2010 | 신생아기에 진단된 미토콘드리아 질환 3례
| Journal of the Korean Society of Neonatology |
| 2010 | Electrocardiography as an early cardiac screening test in children with mitochondrial disease
| Korean Journal of Pediatrics |
| 2010 | 수술 전 뇌 자기공명 영상에서 겉질 형성이상증 소견 보였으나 수술 후 병리학적으로 확인된 해마경화증 1례
| Korean Journal of Pediatrics |
| 2010 | Iron deficiency in children with mitochondrial disease | METABOLIC BRAIN DISEASE |
| 2010 | Initial experiences with proton MR spectroscopy in treatment monitoring of mitochondrial encephalopathy
| YONSEI MEDICAL JOURNAL |
| 2010 | A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiency | BRAIN & DEVELOPMENT |
| 2010 | Caregiver's burden and quality of life in mitochondrial disease | PEDIATRIC NEUROLOGY |
| 2009 | 소아 뇌갈림증의 신경영상학적 소견 및 임상 양상
| Korean Journal of Pediatrics |
| 2009 | 소아 사립체 질환에서 시각 유발전위검사의 유용성
| Korean Journal of Pediatrics |
| 2009 | Clinical characteristics of patients with non-specific and non-categorized mitochondrial diseases | ACTA PAEDIATRICA |
| 2009 | Evaluation of renal function in children with mitochondrial respiratory chain complex defect: usefulness of cystatin C | ACTA PAEDIATRICA |
| 2008 | Newly observed thalamic involvement and mutations of the HEXA gene in a Korean patient with juvenile GM2 gangliosidosis. | METABOLIC BRAIN DISEASE |
| 2008 | Neuroradiologic findings in children with mitochondrial disorder: correlation with mitochondrial respiratory chain defects. | EUROPEAN RADIOLOGY |
| 2008 | 소아 청소년 간질에서 토피라메이트와 관련된 인지 기능 장애
| Journal of Korean Epilepsy Society (대한간질학회지) |
| 2008 | 여러 가지 대사질환에서의 간질
| Korean Journal of Pediatrics |
| 2008 | 소아 만성 두통 환자에서의 Magnetic Resonance Angiography 결과 분석
| Journal of the Korean Child Neurology Society |
| 2008 | 피질 이형성증과 미세이형성의 영상 의학적, 전기생리적 및 임상적 차이 | Korean Journal of Pediatric Neurosurgery (대한소아신경외과학회지) |
| 2008 | Changing the paradigm of 1-stage total callosotomy for the treatment of pediatric generalized epilepsy | JOURNAL OF NEUROSURGERY-PEDIATRICS |
| 2008 | 레녹스 가스토 증후군에서 뇌량절제술
| Journal of Korean Epilepsy Society (대한간질학회지) |
| 2008 | Mitochondrial respiratory chain defects: underlying etiology in various epileptic conditions | EPILEPSIA |
| 2007 | 사립체 질환의 이해 | Journal of the Korean Child Neurology Society |
| 2007 | Efficacy and Tolerability of the Ketogenic Diet According to Lipid:Nonlipid Ratios—Comparison of 3:1 with 4:1 Diet | EPILEPSIA |
| 2007 | Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects | EPILEPSIA |
| 2007 | Nonspecific mitochondrial disease with epilepsy in children: diagnostic approaches and epileptic phenotypes | CHILDS NERVOUS SYSTEM |
| 2006 | A Case of Cogential Fiber Type Disproportion With Multiple Anomalies
| Journal of the Korean Child Neurology Society |
| 2006 | Clinical and Laboratorial Characteristics of Korean Children with Mitochondrial Respiratory Chain Defect
| Journal of the Korean Child Neurology Society |
| 2006 | 측두엽 간질의 삼중 병리에 대한 절제술의 경험 | Korean Journal of Pediatric Neurosurgery (대한소아신경외과학회지) |
| 2006 | Neurologic manifestations and treatment of Henoch–Schönlein purpura | BRAIN & DEVELOPMENT |
| 2006 | Analysis of renal biopsies performed in children with abnormal findings in urinary mass screening | ACTA PAEDIATRICA |
| 2006 | Landau-Kleffner syndrome with mitochondrial respiratory chain-complex I deficiency | PEDIATRIC NEUROLOGY |
| 2006 | 대뇌 피질 발달 기형을 동반한 난치성 소아 간질에서 케톤생성 식이요법의 효과
| Korean Journal of Pediatrics |
| 2006 | 영아 연축 환아에서의 발달 평가 결과
| Journal of the Korean Child Neurology Society |
| 2005 | 소아 간질 치료에서 뇌량 전체 절제술의 결과
| Journal of Korean Epilepsy Society (대한간질학회지) |
| 2005 | 영아 연축을 동반한 난치성 간질에 대한 수술치료에 대한 고찰 | Journal of the Korean Child Neurology Society |
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