| 2024-03 |
Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy |
Epilepsia
|
| 2024-02 |
Aetiology and Prognosis of Encephalitis in Korean Children: A Retrospective Single-Centre Study, 2005–2020 |
Yonsei Medical Journal
|
| 2023-12 |
Surgical Treatment of Epilepsy with Bilateral MRI Abnormalities |
World Neurosurgery
|
| 2023-11 |
Population pharmacokinetics of everolimus in patients with seizures associated with focal cortical dysplasia |
Frontiers in Pharmacology
|
| 2023-11 |
Genotypes and phenotypes of DNM1 encephalopathy |
Journal of Medical Genetics
|
| 2023-09 |
Long-term efficacy and safety of adjunctive perampanel in pediatric patients aged 4–19 years with epilepsy: a real-world study |
Scientific Reports
|
| 2023-08 |
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
|
| 2023-07 |
Social Stigma and Discrimination Toward People With Drug Addiction: A National Survey in Korea |
PSYCHIATRY INVESTIGATION
|
| 2023-04 |
Efficacy and Safety of Lamotrigine Adjunctive Therapy in Lennox-Gastaut Syndrome |
Annals of Child Neurology
|
| 2023-02 |
Refractive Errors, Retinal Findings, and Genotype of Tuberous Sclerosis Complex: A Retrospective Cohort Study |
Yonsei Medical Journal
|
| 2023-02 |
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
|
| 2022-12 |
A Patient with Tuberous Sclerosis with Hemimegalencephaly Presenting with Intractable Epilepsy in the Early Neonatal Period: A Case Report |
Perinatology
|
| 2022-12 |
Analysis of trio test in neurodevelopmental disorders |
Frontiers in Pediatrics
|
| 2022-10 |
Clinical Spectrum and Treatment Outcomes of Patients with Developmental and/or Epileptic Encephalopathy with Spike-and-Wave Activation in Sleep |
Annals of Child Neurology
|
| 2022-10 |
Effects of the ketogenic diet therapy in patients with STXBP1-related encephalopathy |
Epilepsy Research
|
| 2022-09 |
Analysis of low-level somatic mosaicism reveals stage and tissue-specific mutational features in human development |
PLoS genetics
|
| 2022-09 |
Effects of Cannabidiol on Adaptive Behavior and Quality of Life in Pediatric Patients With Treatment-Resistant Epilepsy |
Journal of Clinical Neurology
|
| 2022-09 |
Association of hypercalciuria with vitamin D supplementation in patients undergoing ketogenic dietary therapy |
FRONTIERS IN NUTRITION
|
| 2022-08 |
Treatment strategies for Lennox-Gastaut syndrome: outcomes of multimodal treatment approaches |
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS
|
| 2022-07 |
Neurological Symptoms of SARS-CoV-2 Infection in Pediatric Patients |
Annals of Child Neurology
|
| 2022-07 |
Epilepsy with SLC35A2 Brain Somatic Mutations in Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) |
annals of child neurology
|
| 2022-05 |
Epidural grid, a new methodology of invasive intracranial EEG monitoring: A technical note and experience of a single center |
EPILEPSY RESEARCH
|
| 2022-03 |
Generation of mutation-corrected induced pluripotent stem cell lines derived from adrenoleukodystrophy patient by using homology directed repair |
STEM CELL RESEARCH
|
| 2022-01 |
Real-Time Seizure Detection using EEG: A Comprehensive Comparison of Recent Approaches under a Realistic Setting |
Proceedings of Machine Learning Research (PMLR)
|
| 2022-01 |
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
|
| 2022-01 |
Efficacy and prognosis of long-term, high-dose steroid therapy for Lennox–Gastaut syndrome |
EPILEPSY RESEARCH
|
| 2021-12 |
Neuropsychological adverse drug reactions of Remdesivir: Analysis using VigiBase, the WHO global database of individual case safety reports |
EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
|
| 2021-11 |
Reflections on a 38-Day-Old Japanese Encephalitis Patient Born to a Pregnant Traveler in Endemic Area: Strategies for Prevention |
JOURNAL OF THE PEDIATRIC INFECTIOUS DISEASES SOCIETY
|
| 2021-10 |
Robot-assisted stereoelectroencephalography for pediatric epilepsy surgery: The first case in Korea |
Annals of Child Neurology
|
| 2021-08 |
Neuroprotective effect of both synbiotics and ketogenic diet in a pentylenetetrazol-induced acute seizure murine model |
EPILEPSY RESEARCH
|
| 2021-08 |
Long-term results of vagus nerve stimulation in children with Dravet syndrome: Time-dependent, delayed antiepileptic effect |
EPILEPSY RESEARCH
|
| 2021-08 |
Microfluidic device with brain extracellular matrix promotes structural and functional maturation of human brain organoids |
NATURE COMMUNICATIONS
|
| 2021-07 |
Disparate treatment outcomes according to presence of pathogenic mutations in West syndrome |
EPILEPSIA
|
| 2021-07 |
The feasibility of performing multiple burr hole surgery in pediatric moyamoya patients as a response to failed mEDAS |
CHILDS NERVOUS SYSTEM
|
| 2021-06 |
Treatment strategies targeting specific genetic etiologies in epilepsy |
대한의학유전학회지
|
| 2021-04 |
Clinical features and treatment outcomes of seronegative pediatric autoimmune encephalitis |
JOURNAL OF CLINICAL NEUROLOGY
|
| 2021-03 |
Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafish |
HUMAN MOLECULAR GENETICS
|
| 2021-03 |
Comparative proteome research in a zebrafish model for vanishing white matter disease |
International Journal of Molecular Sciences
|
| 2021-02 |
Clinical characteristics of KCNQ2 encephalopathy |
BRAIN & DEVELOPMENT
|
| 2021-01 |
Effects of salbutamol in collagen like tail subunit of asymmetric acetylcholinesterase-related congenital myasthenic syndrome: A first Korean case |
annals of child neurology
|
| 2021-01 |
Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) |
Acta neuropathologica communications
|
| 2021-01 |
Screening of Tuberous Sclerosis-Associated Neuropsychiatric Disorders in Korea Using the TAND Checklist |
annals of child neurology
|
| 2020-12 |
Cannabidiol for Treating Lennox-Gastaut Syndrome and Dravet Syndrome in Korea |
JOURNAL OF KOREAN MEDICAL SCIENCE
|
| 2020-11 |
Re: Autonomic seizure with prominent apnea in patient with SCN8A-related epileptic encephalopathy |
EPILEPSY RESEARCH
|
| 2020-11 |
Epilepsy surgery for pediatric patients with mild malformation of cortical development |
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
|
| 2020-10 |
EEG Characteristics and Diagnostic Implications in Childhood Headache: A Multi-Center Study |
FRONTIERS IN NEUROLOGY
|
| 2020-10 |
The phenotype and treatment of SCN2A-related developmental and epileptic encephalopathy |
EPILEPTIC DISORDERS
|
| 2020-09 |
Sequence-specific prediction of the efficiencies of adenine and cytosine base editors |
NATURE BIOTECHNOLOGY
|
| 2020-08 |
Long-term outcomes of ketogenic diet in patients with tuberous sclerosis complex-derived epilepsy |
EPILEPSY RESEARCH
|
| 2020-07 |
Efficacy and safety of lacosamide in adolescents with lennox-gastaut syndrome |
annals of child neurology
|
| 2020-07 |
genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern |
EPILEPSY RESEARCH
|
| 2020-06 |
Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy |
BRAIN & DEVELOPMENT
|
| 2020-06 |
Reanalysis of Genomic Sequencing Results in a Clinical Laboratory: Advantages and Limitations |
FRONTIERS IN NEUROLOGY
|
| 2020-02 |
Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical Development |
PEDIATRIC NEUROLOGY
|
| 2019-12 |
Precise detection of low-level somatic mutation in resected epilepsy brain tissue. |
ACTA NEUROPATHOLOGICA
|
| 2019-12 |
Genetic and clinical features of SCN8A developmental and epileptic encephalopathy |
EPILEPSY RESEARCH
|
| 2019-10 |
Brain somatic mutations in MTOR reveal translational dysregulations underlying intractable focal epilepsy |
JOURNAL OF CLINICAL INVESTIGATION
|
| 2019-10 |
Optimized Treatment for Infantile Spasms: Vigabatrin versus Prednisolone versus Combination Therapy |
Journal of Clinical Medicine
|
| 2019-10 |
Short- and long-term seizure-free outcomes of dietary treatment in infants according to etiology |
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY
|
| 2019-10 |
Proband-Only Clinical Exome Sequencing for Neurodevelopmental Disabilities |
PEDIATRIC NEUROLOGY
|
| 2019-09 |
Prognostic factors for absence epilepsy in childhood |
annals of child neurology
|
| 2019-06 |
Clobazam as an adjunctive treatment for infantile spasms |
EPILEPSY & BEHAVIOR
|
| 2019-05 |
Aligned Brain Extracellular Matrix Promotes Differentiation and Myelination of Human-Induced Pluripotent Stem Cell-Derived Oligodendrocytes |
ACS APPLIED MATERIALS & INTERFACES
|
| 2019-05 |
Medication self-management and the quality of discharge education among parents of children with epilepsy |
EPILEPSY & BEHAVIOR
|
| 2019-04 |
Generation of an induced pluripotent stem cell (iPSC) line from a 42-year-old adult cerebral type X-linked adrenoleukodystrophy (X-ALD) patient |
STEM CELL RESEARCH
|
| 2019-03 |
Predicting the outcome of critically ill children and adolescents with electroencephalography |
annals of child neurology
|
| 2019-03 |
The use of technical replication for detection of low-level somatic mutations in next-generation sequencing |
NATURE COMMUNICATIONS
|
| 2019-02 |
A Child With Lymphangioma Due to Somatic Mutation in PIK3CA Successfully Treated With Everolimus |
PEDIATRIC NEUROLOGY
|
| 2019-02 |
Epilepsy Surgery for Children With Low-Grade Epilepsy-Associated Tumors: Factors Associated With Seizure Recurrence and Cognitive Function |
PEDIATRIC NEUROLOGY
|
| 2018-12 |
Age-Based Characteristics of West Syndrome in Patients with Mitochondrial Disease |
Journal of the Korean Child Neurology Society(대한소아신경학회지)
|
| 2018-12 |
Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylation |
Neurology: Genetics
|
| 2018-12 |
Early Diagnosis of KBG Syndrome Using Diagnostic Exome Sequencing |
Journal of the Korean Child Neurology Society(대한소아신경학회지)
|
| 2018-12 |
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
|
| 2018-11 |
BRAF somatic mutation contributes to intrinsic epileptogenicity in pediatric brain tumors |
NATURE MEDICINE
|
| 2018-11 |
Rufinamide efficacy and safety in children aged 1-4 years with Lennox-Gastaut syndrome |
BRAIN & DEVELOPMENT
|
| 2018-10 |
Long-term Outcome of Resective Epilepsy Surgery in Patients With Lennox-Gastaut Syndrome |
PEDIATRICS
|