372 results on '"Ko, Tae-Sung"'
Search Results
2. Cleft size and type are associated with development of epilepsy and poor seizure control in patients with schizencephaly
3. Clinical and neuropsychological characteristics of children with epilepsy and attention-deficit/hyperactivity disorder
4. Clinical outcomes of pediatric Anti-NMDA receptor encephalitis
5. Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly
6. Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures
7. Deep learning-based, fully automated, pediatric brain segmentation
8. Neurodevelopmental outcomes in children with prenatally diagnosed corpus callosal abnormalities
9. Attention profiles in childhood absence epilepsy compared with attention-deficit/hyperactivity disorder
10. Electrophysiological network predicts clinical response to vigabatrin in epileptic spasms
11. Diagnosis of Schaaf-Yang syndrome in Korean children with developmental delay and hypotonia
12. Profound Biotinidase Deficiency: A Rare but Treatable Inborn Error of Metabolism in a Neonate with Recurrent Seizures.
13. Development of tablet personal computer-based cognitive training programs for children with developmental disabilities whose cognitive age is less than 4 years
14. Methylome analysis and whole-exome sequencing reveal that brain tumors associated with encephalocraniocutaneous lipomatosis are midline pilocytic astrocytomas
15. Long-Term Pharmacological and Psychosocial Outcomes of Adolescent-Onset Epilepsy: A Single-Center Experience
16. Requirement for Head Magnetic Resonance Imaging in Children Who Present to the Emergency Department With Acute Nontraumatic Visual Disturbance
17. Cannabidiol Treatment for Lennox-Gastaut Syndrome at a Single Tertiary Center in South Korea
18. β-Hydroxybutyrate attenuates NMDA-induced spasms in rats with evidence of neuronal stabilization on MR spectroscopy
19. Structural abnormalities in benign childhood epilepsy with centrotemporal spikes (BCECTS)
20. Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?
21. An interictal EEG can predict the outcome of vagus nerve stimulation therapy for children with intractable epilepsy
22. A potential effect of ganaxolone in an animal model of infantile spasms
23. A Rare Case of Anti-Ma2 Antibody-Mediated Autoimmune Encephalomyelitis in Childhood
24. Phenotypic and Genetic Complexity in Pediatric Movement Disorders
25. Implications of slow waves and shifting epileptiform discharges in Angelman syndrome
26. Effect of cervical stabilizing exercise and abdominal stabilization on longus colli thickness and muscle activity of the sternocleidomastoid and scalene
27. Effects of lamotrigine on cognition and behavior compared to carbamazepine as monotherapy for children with partial epilepsy
28. β-Hydroxybutyrate increases the pilocarpine-induced seizure threshold in young mice
29. The Role of Focal Epilepsy Features in Defining SCN1A Mutation-positive Dravet Syndrome as Generalized and Focal Epilepsy
30. Development of a Risk Predictive Scoring System for Epilepsy in Infants with Paroxysmal Motor Events: A Retrospective Single-Center Study
31. Vagus Nerve Stimulation for Intractable Epilepsy: Outcomes in Children and Adults
32. Electroencephalographic generalized features in idiopathic childhood focal epilepsies
33. Stroke-Like Episodes Associated with Coronavirus Disease 2019 in a Child with MELAS Syndrome
34. Hematopoietic Stem Cell Transplantation-Associated Neurological Complications and Their Brain MR Imaging Findings in a Pediatric Population
35. Risk factors for neurological complications and their correlation with survival following pediatric liver transplantation
36. Identification of FOXG1 mutations in infantile hypotonia and postnatal microcephaly
37. Nusinersen in spinal muscular atrophy type 1 from neonates to young adult: 1-year data from three Asia-Pacific regions
38. Over 10-Year Outcomes of Infantile-Onset Epilepsies
39. The Early Response to Dietary Therapy can Predict the Late Outcome in Children with Intractable Epilepsy
40. Clinical Application of Whole Exome Sequencing to Identify Rare but Remediable Neurologic Disorders
41. Delayed Functional Networks Development and Altered Fast Oscillation Dynamics in a Rat Model of Cortical Malformation
42. The Genetic Relationship between Paroxysmal Movement Disorders and Epilepsy
43. Treatment of Children and Adolescents with Epilepsy with Atomoxetine
44. Altered Structural Network in Newly Onset Childhood Absence Epilepsy
45. Psychological Impact of Quarantine on Caregivers at a Children's Hospital for Contact with Case of COVID-19
46. Clinical Implications of Ketosis in Children with Benign Convulsions with Mild Gastroenteritis
47. Experience of a Single Center in Treating Multiple Manifestations of Tuberous Sclerosis Complex with Everolimus
48. Diagnosis of Tuberous Sclerosis Complex and Epilepsy Outcomes in Children with Fetal Cardiac Rhabdomyoma: A Long Term Follow-up Study
49. Development of a Risk Predictive Scoring System for Epilepsy in Infants with Paroxysmal Motor Events: A Retrospective Single-Center Study.
50. A Child with Delayed Development First Diagnosed with Turner Syndrome and Later with Leigh-like Syndrome
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