178 results on '"Lee, Young Mock"'
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2. Nusinersen demonstrates effectiveness in treating spinal muscular atrophy: findings from a three-year nationwide study in Korea
3. Diagnosis of a Large Ependymal Cyst in a Patient with Severe Macrocephaly and No Neurological Risk Factors.
4. Therapeutic outcome of patients with Lennox–Gastaut syndrome with mitochondrial respiratory chain complex I deficiency.
5. Efficacy of High-Dose Steroid Therapy on Bilateral Total Visual Loss in a Patient with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS).
6. Efficacy of High-Dose Steroid Therapy on Bilateral Total Visual Loss in a Patient with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS)
7. Persistent Trigeminal Subtype of Internal Carotid Artery Agenesis in CHARGE Syndrome
8. Nusinersen for Spinal Muscular Atrophy Type I with Chronic Respiratory Failure: A Retrospective Study in South Korea
9. Nutritional Intervention Through Ketogenic Diet in GLUT1 Deficiency Syndrome
10. A Patient with Doose Syndrome Who Received Low Glycemic Index Treatment
11. A Patient with Pyridoxine-Dependent Epilepsy Who Was Treated with Triple Therapy
12. A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease with Acute Bilateral Total Blindness
13. A Patient with Doose Syndrome Who Received Low Glycemic Index Treatment.
14. A Case of Intellectual Disability without Epilepsy Associated with a Pathogenic Variant of STXBP1
15. A multicenter trial of oxcarbazepine oral suspension monotherapy in children newly diagnosed with partial seizures: A clinical and cognitive evaluation
16. Rufinamide as an adjuvant treatment in children with Lennox-Gastaut syndrome
17. Mitochondrial tRNA His mutation (m.12158A > G) associated with MELAS syndrome
18. Effective application of corpus callosotomy in pediatric intractable epilepsy patients with mitochondrial dysfunction
19. Comparative trial of low- and high-dose zonisamide as monotherapy for childhood epilepsy
20. Usefulness of Magnetic Resonance Spectroscopy for the Initial Diagnosis of Mitochondrial DNA-Associated Leigh Syndrome
21. Association Between Epilepsy and Leigh Syndrome With MT-ND3 Mutation, Particularly the m.10191T>C Point Mutation
22. Point Prevalence and Associated Factors of Hip Displacement in Pediatric Patients With Mitochondrial Disease
23. High-Dose Prednisolone Therapy for Lennox–Gastaut Syndrome Caused by Fentanyl Intoxication-Induced Toxic Leukoencephalopathy
24. Clinical Value of Magnetic Resonance Spectroscopy in the Initial Evaluation of Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
25. Complete Penetrance but Different Phenotypes in a Korean Family with Maternal Interstitial Duplication at 15q11.2-q13.1: A Case Report
26. Unusual Clinical Presentations in a Patient with Novel ADCK3 Variants
27. Toxic Leukoencephalopathy by Accidental Oral Ingestion of an Infant’s Fentanyl Patch
28. FLNA Duplication in a Female Infant with Periventricular Nodular Heterotopia
29. DYNC2H1 variants cause Leber congenital amaurosis without syndromic features
30. Epidemiological Features and Economic Burden of Guillain-Barré Syndrome in South Korea: A Nationwide Population-Based Study
31. Dossier Spécial/Special Topic, Être Dix-huitiémiste en Asie de l’Est (Comptes rendus : Hisayasu Nakagawa, L’Esprit des Lumières en France et au Japon)
32. Usefulness of Magnetic Resonance Spectroscopy for the Initial Diagnosis of Mitochondrial DNA-Associated Leigh Syndrome.
33. High-Dose Prednisolone Therapy for Lennox–Gastaut Syndrome Caused by Fentanyl Intoxication-Induced Toxic Leukoencephalopathy.
34. Identification of Missense ADGRV1 Mutation as a Candidate Genetic Cause of Familial Febrile Seizure 4
35. Incidence of Guillain-Barré Syndrome Is Not Associated with Influenza Vaccination in the Elderly
36. Clinical Characteristics of Early-Onset and Late-Onset Leigh Syndrome
37. Causality Assessment Guidelines for Adverse Events Following Immunization with a Focus on Guillain–Barré Syndrome
38. Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction
39. Mitochondrial respiratory chain defects: Underlying etiology in various epileptic conditions
40. Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects
41. Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations
42. Genotype-phenotype correlations in pediatric patients with myotonic dystrophy type 1
43. Transient and Adult Patients with Neurologic Diseases in the Pediatric Emergency Department: Trends and Characteristics
44. The Usefulness of Muscle Biopsy in Initial Diagnostic Evaluation of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
45. Lennox-Gastaut Syndrome in Mitochondrial Disease
46. The Author Reply: Genetic Data Are a Prerequisite for Interpreting Clinical and Muscle Biopsy Findings in MELAS
47. The Author Reply: Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
48. Correlation of Serum Biomarkers and Magnetic Resonance Spectroscopy in Monitoring Disease Progression in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Due to mtDNA A3243G Mutation
49. KL1333, a Novel NAD+ Modulator, Improves Energy Metabolism and Mitochondrial Dysfunction in MELAS Fibroblasts
50. Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing
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