669 results on '"Kang, Hoon-Chul"'
Search Results
2. L-serine treatment in a patient with refractory epilepsy due to a GRIN2A missense mutation
3. A computational clinical decision-supporting system to suggest effective anti-epileptic drugs for pediatric epilepsy patients based on deep learning models using patient’s medical history
4. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development
5. Long-term efficacy and safety of adjunctive perampanel in pediatric patients aged 4–19 years with epilepsy: a real-world study
6. Real-Time Seizure Detection using EEG: A Comprehensive Comparison of Recent Approaches under a Realistic Setting
7. Identification of etiologies according to baseline clinical features of pediatric new-onset refractory status epilepticus in single center retrospective study
8. Functional brain network analysis using electroencephalography in late-onset Lennox–Gastaut syndrome
9. Surgical Treatment of Epilepsy with Bilateral MRI Abnormalities
10. Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders
11. Effects of the ketogenic diet therapy in patients with STXBP1-related encephalopathy
12. Epidural grid, a new methodology of invasive intracranial EEG monitoring: A technical note and experience of a single center
13. Efficacy and prognosis of long-term, high-dose steroid therapy for Lennox–Gastaut syndrome
14. Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group
15. Aetiology and Prognosis of Encephalitis in Korean Children: A Retrospective Single-Centre Study, 2005–2020
16. Resective Epilepsy Surgery after Corpus Callosotomy in Children with Lennox-Gastaut Syndrome
17. Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy
18. Neuroprotective effect of both synbiotics and ketogenic diet in a pentylenetetrazol-induced acute seizure murine model
19. Long-term results of vagus nerve stimulation in children with Dravet syndrome: Time-dependent, delayed antiepileptic effect
20. The feasibility of performing multiple burr hole surgery in pediatric moyamoya patients as a response to failed mEDAS
21. Clinical characteristics of KCNQ2 encephalopathy
22. Epilepsy surgery for pediatric patients with mild malformation of cortical development
23. Common genes and recurrent causative variants in 957 Asian patients with pediatric epilepsy.
24. Microfluidic device with brain extracellular matrix promotes structural and functional maturation of human brain organoids
25. Frequent SLC35A2 brain mosaicism in mild malformation of cortical development with oligodendroglial hyperplasia in epilepsy (MOGHE)
26. Long-term outcomes of ketogenic diet in patients with tuberous sclerosis complex-derived epilepsy
27. Genetic diagnosis and clinical characteristics by etiological classification in early-onset epileptic encephalopathy with burst suppression pattern
28. Targeted gene panel sequencing in early infantile onset developmental and epileptic encephalopathy
29. Population pharmacokinetics of everolimus in patients with seizures associated with focal cortical dysplasia
30. A machine learning-based quantitative model (LogBB_Pred) to predict the blood-brain barrier permeability (logBB value) of drug compounds
31. The task-oriented Smart Tourism Chatbot Service
32. Sequence-specific prediction of the efficiencies of adenine and cytosine base editors
33. An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development
34. Genetic and clinical features of SCN8A developmental and epileptic encephalopathy
35. Short- and long-term seizure-free outcomes of dietary treatment in infants according to etiology
36. Brain somatic mutations in MTOR reveal translational dysregulations underlying intractable focal epilepsy
37. Precise detection of low-level somatic mutation in resected epilepsy brain tissue
38. Rufinamide efficacy and safety in children aged 1–4 years with Lennox–Gastaut syndrome
39. Vigabatrin and high-dose prednisolone therapy for patients with West syndrome
40. Smart tourism chatbot system using Multi-domain Tourism Information DST
41. Differential effects on sodium current impairments by distinct SCN1A mutations in GABAergic neurons derived from Dravet syndrome patients
42. Targeted gene panel and genotype-phenotype correlation in children with developmental and epileptic encephalopathy
43. BRAF somatic mutation contributes to intrinsic epileptogenicity in pediatric brain tumors
44. Low glycemic index treatment in patients with drug-resistant epilepsy
45. Genotypes and phenotypes ofDNM1encephalopathy
46. Long-term efficacy and safety of adjunctive perampanel in pediatric patients aged 4 – 19 years with drug-resistant epilepsy: a real-world study
47. Efficacy and Safety of Lamotrigine Adjunctive Therapy in Lennox-Gastaut Syndrome
48. Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylation
49. Three-dimensional brain-like microenvironments facilitate the direct reprogramming of fibroblasts into therapeutic neurons
50. A decrease in the incidence of encephalitis in South Korea during the COVID‐19 pandemic: A nationwide study between 2010 and 2021
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