Neuroradiologic findings in children with mitochondrial disorder: correlation with mitochondrial respiratory chain defects.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Works by Lee, Young-Mock
Results: 44
1
2
Central precocious puberty may be a manifestation of endocrine dysfunction in pediatric patients with mitochondrial disease.
- Published in:
- European Journal of Pediatrics, 2021, v. 180, n. 2, p. 425, doi. 10.1007/s00431-020-03804-3
- By:
- Publication type:
- Article
3
KL1333, a Novel NAD<sup>+</sup> Modulator, Improves Energy Metabolism and Mitochondrial Dysfunction in MELAS Fibroblasts.
- Published in:
- Frontiers in Neurology, 2018, p. N.PAG, doi. 10.3389/fneur.2018.00552
- By:
- Publication type:
- Article
4
Genotype‐phenotype analysis of MT‐ATP6‐associated Leigh syndrome.
- Published in:
- Acta Neurologica Scandinavica, 2022, v. 145, n. 4, p. 414, doi. 10.1111/ane.13566
- By:
- Publication type:
- Article
5
Early cardiac evaluation in children with non-specific mitochondrial disease with isolated mitochondrial respiratory chain complex I defect.
- Published in:
- Journal of Paediatrics & Child Health, 2012, v. 48, n. 11, p. 1016, doi. 10.1111/j.1440-1754.2012.02585.x
- By:
- Publication type:
- Article
6
Effective application of corpus callosotomy in pediatric intractable epilepsy patients with mitochondrial dysfunction.
- Published in:
- Therapeutic Advances in Neurological Disorders, 2022, p. 1, doi. 10.1177/17562864221092551
- By:
- Publication type:
- Article
7
Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction.
- Published in:
- Therapeutic Advances in Neurological Disorders, 2020, v. 13, p. N.PAG, doi. 10.1177/1756286419897813
- By:
- Publication type:
- Article
8
Safe and Effective Use of the Ketogenic Diet in Children with Epilepsy and Mitochondrial Respiratory Chain Complex Defects.
- Published in:
- Epilepsia (Series 4), 2007, v. 48, n. 1, p. 82, doi. 10.1111/j.1528-1167.2006.00906.x
- By:
- Publication type:
- Article
9
Focal cerebellar infarction as an initial sign of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes.
- Published in:
- Journal of Inherited Metabolic Disease, 2019, v. 42, n. 3, p. 575, doi. 10.1002/jimd.12020
- By:
- Publication type:
- Article
10
Avascular necrosis after long-term glucocorticoid treatment in MELAS: a cautionary note.
- Published in:
- Journal of Inherited Metabolic Disease, 2018, v. 41, n. 2, p. 277, doi. 10.1007/s10545-017-0110-y
- By:
- Publication type:
- Article
11
Cyclic Vomiting Syndrome as a New Phenotype of Ataxia-Telangiectasia Syndrome.
- Published in:
- 2024
- By:
- Publication type:
- Letter
12
Effect of Flunarizine on Recurrent Status Epilepticus in a Patient with Alternating Hemiplegia of Childhood.
- Published in:
- 2024
- By:
- Publication type:
- Letter
13
Leigh Syndrome with MT-ND5 Mutation and Hypertrophic Cardiomyopathy.
- Published in:
- 2023
- By:
- Publication type:
- Letter
14
Therapeutic outcome of patients with Lennox–Gastaut syndrome with mitochondrial respiratory chain complex I deficiency.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1305404
- By:
- Publication type:
- Article
15
Clinical Efficacy and Safety of the Ketogenic Diet in Patients with Genetic Confirmation of Drug-Resistant Epilepsy.
- Published in:
- Nutrients, 2025, v. 17, n. 6, p. 979, doi. 10.3390/nu17060979
- By:
- Publication type:
- Article
16
Clinical Characteristics of Early-Onset and Late-Onset Leigh Syndrome.
- Published in:
- Frontiers in Neurology, 2020, p. 1, doi. 10.3389/fneur.2020.00267
- By:
- Publication type:
- Article
17
Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations.
- Published in:
- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00496
- By:
- Publication type:
- Article
18
Mitochondria DNA Polymorphisms Are Associated with Susceptibility to Endometriosis.
- Published in:
- DNA & Cell Biology, 2012, v. 31, n. 3, p. 316, doi. 10.1089/dna.2011.1279
- By:
- Publication type:
- Article
19
First case report of effective and safe application of cannabidiol to treat concurrent ALG3-CDG and Lennox–Gastaut Syndrome.
- Published in:
- Neurological Sciences, 2025, v. 46, n. 4, p. 1901, doi. 10.1007/s10072-025-08004-1
- By:
- Publication type:
- Article
20
A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS.
- Published in:
- Neurological Sciences, 2024, v. 45, n. 5, p. 2337, doi. 10.1007/s10072-024-07343-9
- By:
- Publication type:
- Article
21
Association Between Epilepsy and Leigh Syndrome With MT-ND3 Mutation, Particularly the m.10191T>C Point Mutation.
- Published in:
- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.752467
- By:
- Publication type:
- Article
22
Juvenile Myasthenia Gravis in Korea.
- Published in:
- Journal of Child Neurology, 2016, v. 31, n. 14, p. 1561, doi. 10.1177/0883073816666206
- By:
- Publication type:
- Article
23
Mitochondrial tRNA<sup>His</sup> mutation (m.12158A > G) associated with MELAS syndrome.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 4, p. 474, doi. 10.1111/cge.14112
- By:
- Publication type:
- Article
24
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 1, p. 111, doi. 10.1111/cge.13958
- By:
- Publication type:
- Article
25
Nusinersen for spinal muscular atrophy types II and III: a retrospective single-center study in South Korea.
- Published in:
- World Journal of Pediatrics, 2023, v. 19, n. 5, p. 450, doi. 10.1007/s12519-022-00638-x
- By:
- Publication type:
- Article
26
Jacobsen syndrome with bilateral periventricular white matter lesions.
- Published in:
- World Journal of Pediatrics, 2022, v. 18, n. 2, p. 142, doi. 10.1007/s12519-021-00467-4
- By:
- Publication type:
- Article
27
Magnetic resonance spectroscopy in Leigh-MELAS overlap syndrome.
- Published in:
- World Journal of Pediatrics, 2019, v. 15, n. 3, p. 306, doi. 10.1007/s12519-019-00250-6
- By:
- Publication type:
- Article
28
Incidence of Guillain-Barré Syndrome Is Not Associated with Influenza Vaccination in the Elderly.
- Published in:
- Vaccines, 2020, v. 8, n. 3, p. 431, doi. 10.3390/vaccines8030431
- By:
- Publication type:
- Article
29
Causality Assessment Guidelines for Adverse Events Following Immunization with a Focus on Guillain–Barré Syndrome.
- Published in:
- Vaccines, 2020, v. 8, n. 1, p. 101, doi. 10.3390/vaccines8010101
- By:
- Publication type:
- Article
30
Association between Neuroimaging Scores and Clinical Status in Pediatric Patients Diagnosed with Metachromatic Leukodystrophy.
- Published in:
- Annals of Child Neurology, 2024, v. 32, n. 4, p. 219, doi. 10.26815/acn.2024.00542
- By:
- Publication type:
- Article
31
Diagnosis of a Large Ependymal Cyst in a Patient with Severe Macrocephaly and No Neurological Risk Factors.
- Published in:
- 2024
- By:
- Publication type:
- Letter to the Editor
32
Efficacy of High-Dose Steroid Therapy on Bilateral Total Visual Loss in a Patient with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS).
- Published in:
- 2024
- By:
- Publication type:
- Letter to the Editor
33
A Patient with Doose Syndrome Who Received Low Glycemic Index Treatment.
- Published in:
- 2023
- By:
- Publication type:
- Letter to the Editor
34
A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease with Acute Bilateral Total Blindness.
- Published in:
- 2022
- By:
- Publication type:
- Letter
35
A Patient with Pyridoxine-Dependent Epilepsy Who Was Treated with Triple Therapy.
- Published in:
- 2022
- By:
- Publication type:
- Letter to the Editor
36
A Case of Intellectual Disability without Epilepsy Associated with a Pathogenic Variant of STXBP1.
- Published in:
- 2022
- By:
- Publication type:
- Letter
37
Usefulness of Magnetic Resonance Spectroscopy for the Initial Diagnosis of Mitochondrial DNA-Associated Leigh Syndrome.
- Published in:
- Annals of Child Neurology, 2022, v. 30, n. 1, p. 17, doi. 10.26815/acn.2021.00542
- By:
- Publication type:
- Article
38
High-Dose Prednisolone Therapy for Lennox–Gastaut Syndrome Caused by Fentanyl Intoxication-Induced Toxic Leukoencephalopathy.
- Published in:
- 2022
- By:
- Publication type:
- Letter
39
Clinical Value of Magnetic Resonance Spectroscopy in the Initial Evaluation of Patients with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes.
- Published in:
- Annals of Child Neurology, 2021, v. 29, n. 3, p. 140, doi. 10.26815/acn.2021.00381
- By:
- Publication type:
- Article
40
Unusual Clinical Presentations in a Patient with Novel ADCK3 Variants.
- Published in:
- 2021
- By:
- Publication type:
- Letter
41
Toxic Leukoencephalopathy by Accidental Oral Ingestion of an Infant's Fentanyl Patch.
- Published in:
- 2021
- By:
- Publication type:
- Letter
42
FLNA Duplication in a Female Infant with Periventricular Nodular Heterotopia.
- Published in:
- 2021
- By:
- Publication type:
- Letter to the Editor
43
Diagnosis and Management of Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Syndrome.
- Published in:
- Biomolecules (2218-273X), 2024, v. 14, n. 12, p. 1524, doi. 10.3390/biom14121524
- By:
- Publication type:
- Article
44
Efficient strategy for the molecular diagnosis of intractable early-onset epilepsy using targeted gene sequencing.
- Published in:
- BMC Medical Genomics, 2018, v. 11, p. 1, doi. 10.1186/s12920-018-0320-7
- By:
- Publication type:
- Article