ScholarWorks@Korea University: Eun, Baik Lin

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Eun, Baik Lin (은백린)

College of Medicine (Department of Medical Science)

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Tel 구3153
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Child:14||Epilepsy:7||Korea:5||Cognition:3||Infant:3||child:3||Newborn:3||Behavior:3||Encephalitis:2||Oxcarbazepine:2||Body image:2||Weight loss:2||Magnetic resonance:2||Eating disorders:2||Cerebral ischemia:2||Developmental surveillance:2||National health programs:2||Seizures:2||epilepsy:2||Health insurance:2||Headache:2||Adolescent:2||Female:2||prevalence:2||VPS33B:1||Mutation:1||febrile seizure:1||meningitis:1||recurrence:1||rat:1||absence seizures:1||febrile seizures:1||peripheral nervous system diseases:1||neuroimaging:1||Mesenchymal stem cell:1||Health policy:1||Obesity:1||Herbal medicine:1||VideoEEG monitoring:1||nutritional support:1||Personal satisfaction:1||Brain inflammation:1||temporal lobe epilepsy:1||Hypoxicischemic encephalopathy:1||Movement disorders:1||encephalomyelitis:1||SaethreChotzen syndrome:1||Lamotrigine:1||Rufinamide:1||school children:1||headache:1||Neural precursors:1||Globally ischemic brain:1||Counseling:1||Seizure:1||brain:1||hypoxiaischemia:1||neuroprotection:1||Gastroenteritis:1||cytokines:1||Social competence:1||School competence:1||Array comparative genomic hybridization:1||Enterovirus 71:1||Psychological factors:1||Prognosis:1||Nutrition:1||Children:1||Questionnaire:1||growth:1||Whole exome sequencing:1||Neurodevelopmental delay:1||lumbar puncture:1||seizures:1||lacosamide:1||Fellow:1||Training environment:1||Febrile seizure:1||Xlinked CharcotMarieTooth disease:1||Pseudodeficiency:1||Genetic mutation:1||Respiratory syncytial virus:1||Microdeletion:1||Human placental extract:1||Attention Deficit Disorder with Hyperactivity:1||Intellectual Disability:1||Embryonic stem cells:1||Abducens nerve diseases:1||national health programs:1||developmental surveillance:1||Psychosocial function:1||General adaptive function:1||anticonvulsants:1||nervous system disease:1||Neuroprotection:1||Breastfeeding:1||Reanalysis:1||population:1||Curriculum:1||Pediatric:1||valproic acid:1||microglia:1||Hippocampal injury:1||Gap junctions:1||ADEM:1||Start codon mutation:1||Arylsulfatase A:1||Vitamin D:1||Comparative genomic hybridization:1||TWIST:1||LennoxGastaut syndrome:1||primary headache:1||guideline:1||children:1||Treatment:1||Safety:1||malnutrition:1||COVID19 Pandemic:1||Pediatric Patient:1||Neonatal cholestasis:1||VIPAR:1||newborn:1||Norovirus:1||prognostic factors:1||lipopolysaccharide:1||Connexin32:1||CharcotMarieTooth disease:1||developmental disabilities:1||intellectual disability:1||Partial epilepsy:1||Sleep:1||infant:1||Paroxysmal nonepileptic event:1||gastrostomy:1||Severity of Illness:1||Preventive Measures:1||Magnesium:1||Febrile:1||febrile:1||lamotrigine:1||Genetics  clinical:1||Metachromatic leukodystrophy:1||Behavioral problems:1||Quality of life:1||connexin 32:1||acute disseminated:1||Zonisamide:1||Cell transplantation:1||Efficacy:1||

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145 Anam-ro, Seongbuk-gu, Seoul, 02841, Korea+82-2-3290-2963

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