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Abnormal Electroencephalogram Findings and Its Correlation With Clinical Features From Pediatric Patients in Psychiatric Clinic.
- Published in:
- Clinical EEG & Neuroscience, 2024, v. 55, n. 6, p. 636, doi. 10.1177/15500594241256170
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- Article
Diagnostic Yield of Epilepsy Panel Testing in Patients With Seizure Onset Within the First Year of Life.
- Published in:
- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00988
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- Publication type:
- Article
Deep Convolutional Neural Network Based Interictal-Preictal Electroencephalography Prediction: Application to Focal Cortical Dysplasia Type-II.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.594679
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- Publication type:
- Article
Characterization of Anti-seizure Medication Treatment Pathways in Pediatric Epilepsy Using the Electronic Health Record-Based Common Data Model.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00409
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- Article
A Unique Mutational Spectrum of MLC1 in Korean Patients With Megalencephalic Leukoencephalopathy With Subcortical Cysts: p.Ala275Asp Founder Mutation and Maternal Uniparental Disomy of Chromosome 22.
- Published in:
- Annals of Laboratory Medicine, 2017, v. 37, n. 6, p. 516, doi. 10.3343/alm.2017.37.6.516
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- Article
The Korean undiagnosed diseases program: lessons from a one-year pilot project.
- Published in:
- 2019
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- Publication type:
- journal article
Serum α-synuclein and IL-1β are increased and correlated with measures of disease severity in children with epilepsy: potential prognostic biomarkers?
- Published in:
- 2020
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- Publication type:
- journal article
Cord blood transforming growth factor-β-induced as predictive biomarker of retinopathy of prematurity in preterm infants.
- Published in:
- Graefe's Archive of Clinical & Experimental Ophthalmology, 2023, v. 261, n. 9, p. 2477, doi. 10.1007/s00417-023-06056-7
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- Publication type:
- Article
Clinico‐radiological characteristics of anti‐myelin oligodendrocyte glycoprotein antibody‐associated autoimmune encephalitis in children.
- Published in:
- Developmental Medicine & Child Neurology, 2022, v. 64, n. 8, p. 998, doi. 10.1111/dmcn.15174
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- Publication type:
- Article
Deep learning-based automated detection and multiclass classification of focal interictal epileptiform discharges in scalp electroencephalograms.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33906-5
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- Publication type:
- Article
The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure.
- Published in:
- 2022
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- Publication type:
- journal article
Importance of early diagnosis in LMNA-related muscular dystrophy for cardiac surveillance.
- Published in:
- 2019
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- Publication type:
- journal article
Consecutive analysis of mutation spectrum in the dystrophin gene of 507 Korean boys with Duchenne/Becker muscular dystrophy in a single center.
- Published in:
- 2017
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- Publication type:
- journal article
Big data analysis and artificial intelligence in epilepsy -- common data model analysis and machine learning-based seizure detection and forecasting.
- Published in:
- Clinical & Experimental Pediatrics, 2022, v. 65, n. 6, p. 272, doi. 10.3345/cep.2021.00766
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- Publication type:
- Article
Complex Febrile Seizures in Children with COVID-19 Infection.
- Published in:
- 2023
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- Publication type:
- Letter
Generalized Tonic-Clonic Seizures after Self-Limited Epilepsy with Centrotemporal Spikes: A Case Series.
- Published in:
- Annals of Child Neurology, 2022, v. 30, n. 4, p. 173, doi. 10.26815/acn.2022.00115
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- Publication type:
- Article
Heterogeneous Clinical Characteristics of Allan-Herndon-Dudley Syndrome with SLC16A2 Mutations.
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- Annals of Child Neurology, 2021, v. 29, n. 4, p. 149, doi. 10.26815/acn.2021.00423
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- Publication type:
- Article
Clinical and Genetic Spectrum of STXBP1 Encephalopathy in the Korean Pediatric Population.
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- Annals of Child Neurology, 2021, v. 29, n. 2, p. 68, doi. 10.26815/acn.2020.00304
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- Publication type:
- Article
Deep Phenotyping in 1p36 Deletion Syndrome.
- Published in:
- Annals of Child Neurology, 2020, v. 28, n. 4, p. 131, doi. 10.26815/acn.2020.00108
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- Publication type:
- Article
Short Course and Early Switch of Vigabatrin for Infantile spasms.
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- Annals of Child Neurology, 2020, v. 28, n. 3, p. 88, doi. 10.26815/acn.2020.00059
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- Publication type:
- Article
Perception simplex: Verifiable collision avoidance in autonomous vehicles amidst obstacle detection faults.
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- Software Testing: Verification & Reliability, 2024, v. 34, n. 6, p. 1, doi. 10.1002/stvr.1879
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- Publication type:
- Article
Outcomes of the second withdrawal of anti‐seizure medication in patients with pediatric‐onset epilepsy.
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- Epilepsia (Series 4), 2023, v. 64, n. 6, p. e93, doi. 10.1111/epi.17594
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- Publication type:
- Article
Analysis of antiseizure drug‐related adverse reactions from the electronic health record using the common data model.
- Published in:
- Epilepsia (Series 4), 2020, v. 61, n. 4, p. 610, doi. 10.1111/epi.16472
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- Publication type:
- Article
First Successful Application of Preimplantation Genetic Diagnosis for Lethal Neonatal Rigidity and Multifocal Seizure Syndrome in Korea: A Case Report.
- Published in:
- Neonatal Medicine, 2022, v. 29, n. 4, p. 141, doi. 10.5385/nm.2022.29.4.141
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- Article
Epilepsy phenotype and gene ontology analysis of the 129 genes in a large neurodevelopmental disorders cohort.
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- Frontiers in Neurology, 2023, p. 1, doi. 10.3389/fneur.2023.1218706
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- Publication type:
- Article
SYNGAP1‐related developmental and epileptic encephalopathy: Genotypic and phenotypic characteristics and longitudinal insights.
- Published in:
- American Journal of Medical Genetics. Part A, 2024, v. 194, n. 8, p. 1, doi. 10.1002/ajmg.a.63606
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- Publication type:
- Article
Single-channel seizure detection with clinical confirmation of seizure locations using CHB-MIT dataset.
- Published in:
- Frontiers in Neurology, 2024, p. 01, doi. 10.3389/fneur.2024.1389731
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- Publication type:
- Article
Genetic diagnosis of infantile‐onset epilepsy in the clinic: Application of whole‐exome sequencing following epilepsy gene panel testing.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 3, p. 418, doi. 10.1111/cge.13903
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- Publication type:
- Article
A 13-year-old girl with proximal weakness and hypertrophic cardiomyopathy with danon disease.
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- Muscle & Nerve, 2010, v. 41, n. 6, p. 879, doi. 10.1002/mus.21614
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- Publication type:
- Article