Browsing by Yonsei Author : Kang, Hoon Chul

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Name:
Kang, Hoon Chul [강훈철]
orcid http://orcid.org/0000-0002-3659-8847
Department :
College of Medicine (의과대학) - Dept. of Pediatrics (소아과학교실)
Scopus ID :
Scopus (34770080800)

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Issue DateTitleJournal Title
2023Surgical Treatment of Epilepsy with Bilateral MRI AbnormalitiesWORLD NEUROSURGERY
2023Long-term efficacy and safety of adjunctive perampanel in pediatric patients aged 4-19 years with epilepsy: a real-world study SCIENTIFIC REPORTS
2023Acute Necrotizing Myelitis Associated with COVID-19 YONSEI MEDICAL JOURNAL
2023Population pharmacokinetics of everolimus in patients with seizures associated with focal cortical dysplasia FRONTIERS IN PHARMACOLOGY
2023A machine learning-based quantitative model (LogBB_Pred) to predict the blood-brain barrier permeability (logBB value) of drug compounds BIOINFORMATICS
2023Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental DisordersJOURNAL OF MOLECULAR DIAGNOSTICS
2023Social Stigma and Discrimination Toward People With Drug Addiction: A National Survey in Korea PSYCHIATRY INVESTIGATION
2023Genotypes and phenotypes of DNM1 encephalopathyJOURNAL OF MEDICAL GENETICS
2023Efficacy and Safety of Lamotrigine Adjunctive Therapy in Lennox-Gastaut Syndrome Annals of Child Neurology
2023Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development NATURE GENETICS
2023Refractive Errors, Retinal Findings, and Genotype of Tuberous Sclerosis Complex: A Retrospective Cohort Study YONSEI MEDICAL JOURNAL
2023A decrease in the incidence of encephalitis in South Korea during the COVID‐19 pandemic: A nationwide study between 2010 and 2021JOURNAL OF MEDICAL VIROLOGY
2023Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene NEUROLOGY
2022A Patient with Tuberous Sclerosis with Hemimegalencephaly Presenting with Intractable Epilepsy in the Early Neonatal Period: A Case Report Perinatology
2022Analysis of trio test in neurodevelopmental disorders FRONTIERS IN PEDIATRICS
2022Effects of the ketogenic diet therapy in patients with STXBP1-related encephalopathyEPILEPSY RESEARCH
2022Clinical Spectrum and Treatment Outcomes of Patients with Developmental and/or Epileptic Encephalopathy with Spike-and-Wave Activation in Sleep Annals of Child Neurology
2022Analysis of low-level somatic mosaicism reveals stage and tissue-specific mutational features in human development PLOS GENETICS
2022Effects of Cannabidiol on Adaptive Behavior and Quality of Life in Pediatric Patients With Treatment-Resistant Epilepsy JOURNAL OF CLINICAL NEUROLOGY
2022Association of hypercalciuria with vitamin D supplementation in patients undergoing ketogenic dietary therapy FRONTIERS IN NUTRITION
2022Treatment strategies for Lennox-Gastaut syndrome: outcomes of multimodal treatment approaches THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS
2022Epilepsy with SLC35A2 Brain Somatic Mutations in Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Epilepsy (MOGHE) Annals of Child Neurology
2022Neurological Symptoms of SARS-CoV-2 Infection in Pediatric Patients Annals of Child Neurology
2022A Mixed-Lipid Diet (Medium-Chain and Long-Chain Triglycerides) for Better Tolerability and Efficiency in Pediatric Epilepsy Patients Annals of Child Neurology
2022Epidural grid, a new methodology of invasive intracranial EEG monitoring: A technical note and experience of a single centerEPILEPSY RESEARCH
2022Generation of mutation-corrected induced pluripotent stem cell lines derived from adrenoleukodystrophy patient by using homology directed repair STEM CELL RESEARCH
2022Real-Time Seizure Detection using EEG: A Comprehensive Comparison of Recent Approaches under a Realistic Setting Proceedings of Machine Learning Research
2022Efficacy of the Ketogenic Diet for Pediatric Epilepsy According to the Presence of Detectable Somatic mTOR Pathway Mutations in the Brain JOURNAL OF CLINICAL NEUROLOGY
2022Efficacy and prognosis of long-term, high-dose steroid therapy for Lennox-Gastaut syndromeEPILEPSY RESEARCH
2021Neuropsychological adverse drug reactions of Remdesivir: analysis using VigiBase, the WHO global database of individual case safety reports EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES
2021Reflections on a 38-Day-Old Japanese Encephalitis Patient Born to a Pregnant Traveler in Endemic Area: Strategies for PreventionJOURNAL OF THE PEDIATRIC INFECTIOUS DISEASES SOCIETY
2021중추신경흥분성 식욕억제제 사용의 부작용에 관한 신속 체계적 문헌고찰: 의존 및 정신병 중심으로Journal of Korean Academy fo Addiction Psychiatry(중독정신의학)
2021Robot-Assisted Stereoelectroencephalography for Pediatric Epilepsy Surgery: The First Case in Korea Annals of Child Neurology
2021Long-term results of vagus nerve stimulation in children with Dravet syndrome: Time-dependent, delayed antiepileptic effect EPILEPSY RESEARCH
2021Neuroprotective effect of both synbiotics and ketogenic diet in a pentylenetetrazol-induced acute seizure murine modelEPILEPSY RESEARCH
2021Microfluidic device with brain extracellular matrix promotes structural and functional maturation of human brain organoids NATURE COMMUNICATIONS
2021Disparate treatment outcomes according to presence of pathogenic mutations in West syndromeEPILEPSIA
2021The feasibility of performing multiple burr hole surgery in pediatric moyamoya patients as a response to failed mEDASCHILDS NERVOUS SYSTEM
2021Treatment strategies targeting specific genetic etiologies in epilepsy Journal of Genetic Medicine(대한의학유전학회지)
2021Eif2b3 mutants recapitulate phenotypes of vanishing white matter disease and validate novel disease alleles in zebrafishHUMAN MOLECULAR GENETICS
2021Clinical Features and Treatment Outcomes of Seronegative Pediatric Autoimmune Encephalitis JOURNAL OF CLINICAL NEUROLOGY
2021Comparative Proteome Research in a Zebrafish Model for Vanishing White Matter Disease INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
2021Clinical characteristics of KCNQ2 encephalopathyBRAIN & DEVELOPMENT
2021Effects of Salbutamol in Collagen like Tail Subunit of Asymmetric Acetylcholinesterase-Related Congenital Myasthenic Syndrome: A First Korean Case Annals of Child Neurology
2021Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) ACTA NEUROPATHOLOGICA COMMUNICATIONS
2021Screening of Tuberous Sclerosis-Associated Neuropsychiatric Disorders in Korea Using the TAND Checklist Annals of Child Neurology
2020Cannabidiol for Treating Lennox-Gastaut Syndrome and Dravet Syndrome in Korea JOURNAL OF KOREAN MEDICAL SCIENCE
2020Re: Autonomic seizure with prominent apnea in patient with SCN8A-related epileptic encephalopathyEPILEPSY RESEARCH
2020Epilepsy surgery for pediatric patients with mild malformation of cortical developmentSEIZURE-EUROPEAN JOURNAL OF EPILEPSY
2020EEG Characteristics and Diagnostic Implications in Childhood Headache: A Multi-Center Study FRONTIERS IN NEUROLOGY

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