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Unusual Clinical Presentations in a Patient with Novel ADCK3 Variants

Huh ER, Lee H, Lee YM

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Toxic Leukoencephalopathy by Accidental Oral Ingestion of an Infant’s Fentanyl Patch

Lim H, Lee H, Lee YM

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FLNA Duplication in a Female Infant with Periventricular Nodular Heterotopia

Kong NS, Lee H, Lee YM

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Clinical Manifestations of Hydranencephaly: A Case in Monochorionic-Diamniotic Twin

Kim BG, Lim KJ, Yi YY

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Anticonvulsants for the Treatment of Hemichorea after Surgical Revascularization in Adolescent Patients with Moyamoya Disease

Lee GH, Kim DH, Park HS, Jang WR, Kwon YS

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A MAST1 Mutation Underlying Mega-Corpus Callosum Syndrome with Extended Phenotypes: The First Case in Korea

Hur YJ, Chung WY, Lim YJ, Park S, Jun KR

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Characteristics of Meningitis in Febrile Infants Aged ≤90 Days

Cho KU, You SJ

Purpose: This study evaluated the clinical and laboratory characteristics of infants ≤90 days old with meningitis who presented to the hospital with a fever. We also investigated whether initial C-reactive...
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Comparison of the Demographics and Ratio of Rotavirus-Associated Benign Convulsions with Mild Gastroenteritis to Rotavirus Gastroenteritis before and after Rotavirus Vaccination over a Period of 20 Years

Lee YS, Kim DH, Ha DJ, Kwon YS

Purpose: Through a study of rotavirus gastroenteritis (RVGE) cases experienced over 20 years at our center, we aimed to investigate changes in the ratio of rotavirus-associated benign convulsions with mild...
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Once-Daily Extended-Release Levetiracetam Improves Medication Compliance in Adolescent Epilepsy Patients

Jung SY, Yi YY, Kang JW

Purpose: Since pharmacologic agents are the mainstay of epilepsy treatment, drug compliance is one of the most important factors in seizure control. Once-daily levetiracetam (LEV) has been proven to have...
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Clinical and Genetic Spectrum of STXBP1 Encephalopathy in the Korean Pediatric Population

Kim WJ, Shim YK, Ko YJ, Kim SY, Kim H, Lim BC, Hwang H, Choi J, Kim KJ, Chae JH

Purpose: Syntaxin-binding protein 1 (STXBP1) mutations are known to result in various phenotypes including Ohtahara syndrome, West syndrome, and autism, collectively referred as STXBP1 encephalopathy. This study aimed to expand...
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