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
2021Microfluidic device with brain extracellular matrix promotes structural and functional maturation of human brain organoids NATURE COMMUNICATIONS
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
2021Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE) ACTA NEUROPATHOLOGICA COMMUNICATIONS
2020Screening 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
2020The phenotype and treatment of SCN2A-related developmental and epileptic encephalopathyEPILEPTIC DISORDERS
2020Sequence-specific prediction of the efficiencies of adenine and cytosine base editorsNATURE BIOTECHNOLOGY
2020Long-term outcomes of ketogenic diet in patients with tuberous sclerosis complex-derived epilepsyEPILEPSY RESEARCH
2020Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression patternEPILEPSY RESEARCH
2020Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathyBRAIN & DEVELOPMENT
2020Reanalysis of Genomic Sequencing Results in a Clinical Laboratory: Advantages and Limitations FRONTIERS IN NEUROLOGY
2020Clinical Implementation of Targeted Gene Sequencing for Malformation of Cortical DevelopmentPEDIATRIC NEUROLOGY
2019Generation 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
2019Precise detection of low-level somatic mutation in resected epilepsy brain tissueACTA NEUROPATHOLOGICA
2019Genetic and clinical features of SCN8A developmental and epileptic encephalopathyEPILEPSY RESEARCH
2019Brain somatic mutations in MTOR reveal translational dysregulations underlying intractable focal epilepsyJOURNAL OF CLINICAL INVESTIGATION
2019Proband-Only Clinical Exome Sequencing for Neurodevelopmental DisabilitiesPEDIATRIC NEUROLOGY
2019Optimized Treatment for Infantile Spasms: Vigabatrin versus Prednisolone versus Combination Therapy Journal of Clinical Medicine
2019Short- and long-term seizure-free outcomes of dietary treatment in infants according to etiologySeizure - European Journal of Epilepsy
2019Clobazam as an adjunctive treatment for infantile 넴는Epilepsy & Behavior
2019A Child With Lymphangioma Due to Somatic Mutation in PIK3CA Successfully Treated With EverolimusPEDIATRIC NEUROLOGY
2019The use of technical replication for detection of low-level somatic mutations in next-generation sequencing NATURE COMMUNICATIONS
2019Aligned Brain Extracellular Matrix Promotes Differentiation and Myelination of Human-Induced Pluripotent Stem Cell-Derived OligodendrocytesACS APPLIED MATERIALS & INTERFACES
2019Epilepsy Surgery for Children With Low-Grade Epilepsy-Associated Tumors: Factors Associated With Seizure Recurrence and Cognitive FunctionPEDIATRIC NEUROLOGY
2018BRAF somatic mutation contributes to intrinsic epileptogenicity in pediatric brain tumorsNATURE MEDICINE
2018미토콘드리아 질환에서 웨스트 증후군 환자의 경련 발생 연령에 따른 임상 양상 비교 Journal of the Korean Child Neurology Society
2018Rufinamide efficacy and safety in children aged 1-4 years with Lennox-Gastaut syndromeBRAIN & DEVELOPMENT
2018Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylationNEUROLOGY-GENETICS
2018Diagnostic exome sequencing을 통한 KBG 증후군의 조기 진단 Journal of the Korean Child Neurology Society
2018Long-term Outcome of Resective Epilepsy Surgery in Patients With Lennox-Gastaut SyndromePEDIATRICS
2018Interregional 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 studyEPILEPSIA
2018Brain Somatic Mutations in MTOR Disrupt Neuronal Ciliogenesis, Leading to Focal Cortical DyslaminationNEURON
2018Vigabatrin and high-dose prednisolone therapy for patients with West syndromeEPILEPSY RESEARCH
2018Three-dimensional brain-like microenvironments facilitate the direct reprogramming of fibroblasts into therapeutic neuronsNATURE BIOMEDICAL ENGINEERING
2018The efficacy of ketogenic diet for specific genetic mutation in developmental and epileptic encephalopathy FRONTIERS IN NEUROLOGY
2018Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group EPILEPSIA
2018Adverse Events During Perampanel Adjunctive Therapy in Intractable Epilepsy JOURNAL OF CLINICAL NEUROLOGY
2018Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patientsBRAIN & DEVELOPMENT
2018Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathyEPILEPSY RESEARCH
2018Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing BMC MEDICAL GENOMICS
2018Efficacy of Stiripentol in Dravet Syndrome with or without SCN1A Mutations JOURNAL OF CLINICAL NEUROLOGY
2017Alpers-Huttenlocher Syndrome First Presented with Hepatic Failure: Can Liver Transplantation Be Considered as Treatment Option? PEDIATRIC GASTROENTEROLOGY HEPATOLOGY & NUTRITION
2017Generation of two induced pluripotent stem cell (iPSC) lines from X-linked adrenoleukodystrophy (X-ALD) patients with adrenomyeloneuropathy (AMN) STEM CELL RESEARCH
2017Mowat-Wilson syndrome presenting with fever-associated seizuresEPILEPTIC DISORDERS

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