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Clinical Impact of Coronavirus Disease 2019 Outbreaks in Korea on Seizures in Children.
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- Annals of Child Neurology, 2024, v. 32, n. 3, p. 154, doi. 10.26815/acn.2024.00465
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- Article
The Wide Variety of Acute Disseminated Encephalomyelitis in Children: A Clinical Perspective.
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- Annals of Child Neurology, 2022, v. 30, n. 4, p. 155, doi. 10.26815/acn.2022.00220
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- Article
Clinical Characteristics of Epilepsy and Its Risk Factors in Neurofibromatosis Type 1: A Single-Center Study.
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- Annals of Child Neurology, 2021, v. 29, n. 1, p. 1, doi. 10.26815/acn.2020.00283
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- Article
Clinical Spectrum of Posterior Reversible Encephalopathy Syndrome in Children.
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- Annals of Child Neurology, 2020, v. 28, n. 2, p. 43, doi. 10.26815/acn.2020.00031
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- Article
Changes of lysosome by L-serine in rotenone-treated hippocampal neurons.
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- Applied Microscopy, 2023, v. 53, n. 1, p. 1, doi. 10.1186/s42649-022-00084-z
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- Article
Population Pharmacokinetic Model of AST-001, L-Isomer of Serine, Combining Endogenous Production and Exogenous Administration in Healthy Subjects.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.891227
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- Article
Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic Studies.
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- Journal of Korean Neurosurgical Society, 2016, v. 59, n. 3, p. 214, doi. 10.3340/jkns.2016.59.3.214
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- Article
Mutations of the SCN1A gene in acute encephalopathy.
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- Epilepsia (Series 4), 2012, v. 53, n. 3, p. 558, doi. 10.1111/j.1528-1167.2011.03402.x
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- Article
Restoration of Cathepsin D Level via L-Serine Attenuates PPA-Induced Lysosomal Dysfunction in Neuronal Cells.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810613
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- Article
Sirtuin 3 mutation- induced mitochondrial dysfunction and optic neuropathy: a case report.
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- 2023
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- Case Study
Variation in clinical usefulness of biomarkers of acute kidney injury in young children undergoing cardiac surgery.
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- Clinical & Experimental Pediatrics, 2020, v. 63, n. 4, p. 151, doi. 10.3345/cep.2019.00913
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- Article
Cohen Syndrome Patient iPSC-Derived Neurospheres and Forebrain-Like Glutamatergic Neurons Reveal Reduced Proliferation of Neural Progenitor Cells and Altered Expression of Synapse Genes.
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- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1886, doi. 10.3390/jcm9061886
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- Article
The molecular pathophysiology of vascular anomalies: Genomic research.
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- Archives of Plastic Surgery, 2020, v. 47, n. 3, p. 203, doi. 10.5999/aps.2020.00591
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- Article
Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation.
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- Journal of Human Genetics, 2011, v. 56, n. 8, p. 609, doi. 10.1038/jhg.2011.69
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- Article
Early Diagnosis of ABCB11 Spectrum Liver Disorders by Next Generation Sequencing.
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- Pediatric Gastroenterology, Hepatology & Nutrition, 2017, v. 20, n. 2, p. 114, doi. 10.5223/pghn.2017.20.2.114
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- Article
G 1 Cell Cycle Arrest and Extrinsic Apoptotic Mechanisms Underlying the Anti-Leukemic Activity of CDK7 Inhibitor BS-181.
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- Cancers, 2020, v. 12, n. 12, p. 3845, doi. 10.3390/cancers12123845
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- Article
Early Diagnosis of Pseudohypoparathyroidism before the Development of Hypocalcemia in a Young Infant.
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- Children, 2022, v. 9, n. 5, p. 723, doi. 10.3390/children9050723
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- Article
Atypical Presentation of Enlarged Vestibular Aqueducts Caused by SLC26A4 Variants.
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- Children, 2022, v. 9, n. 2, p. 165, doi. 10.3390/children9020165
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- Article
Clinical experience of nusinersen in a broad spectrum of spinal muscular atrophy: A retrospective study.
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- Annals of Indian Academy of Neurology, 2020, v. 23, n. 6, p. 796, doi. 10.4103/aian.AIAN_524_20
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- Article
Congenital abnormalities of the retinal vasculature in neurofibromatosis type I.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-69852-9
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- Article
Identification of Candidate Gene Variants in Korean MODY Families by Whole-Exome Sequencing.
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- Hormone Research in Paediatrics, 2015, v. 83, n. 4, p. 242, doi. 10.1159/000368657
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- Article
Everolimus improves neuropsychiatric symptoms in a patient with tuberous sclerosis carrying a novel TSC2 mutation.
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- Molecular Brain, 2016, v. 9, p. 1, doi. 10.1186/s13041-016-0222-6
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- Article
AST-001 Improves Social Deficits and Restores Dopamine Neuron Activity in a Mouse Model of Autism.
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- Biomedicines, 2023, v. 11, n. 12, p. 3283, doi. 10.3390/biomedicines11123283
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- Article
KCNQ2 Encephalopathy Showing a Distinct Ictal Amplitude- Integrated Electroencephalographic Pattern.
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- Neonatal Medicine, 2020, v. 27, n. 4, p. 202, doi. 10.5385/nm.2020.27.4.202
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- Article