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Mineralizing Angiopathy: An Uncommon Cause of Pediatric Stroke with Good Outcome

Nagabushana D, Chandrasekhar S, Venkatesha GA

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High-Dose Prednisolone Therapy for Lennox–Gastaut Syndrome Caused by Fentanyl Intoxication-Induced Toxic Leukoencephalopathy

Shin HJ, Na JH, Lee H, Lee YM

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Unilateral and Reversible Hypoglossal Nerve Palsy Due to Infectious Mononucleosis

Na JH, Lee JH

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Distinctive Severe Ocular Abnormalities and Epilepsy Accompanied by a Novel ZEB2 Mutation in a Child with Mowat-Wilson Syndrome

Park S, Hur YJ, Yoon JS, Jang MA

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A Juvenile Case of Primary Sjögren Syndrome Presenting as Limb Weakness

Baik SJ, Han TH, Jung SY, Bang JI, Chae KY

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Neonatal-Onset PIGT Encephalopathy: A Rare Korean Case with Hypophosphatasia

Chun MJ, Moon YS, Jang WR, Chae JH, Kwon YS

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Development of a Risk Predictive Scoring System for Epilepsy in Infants with Paroxysmal Motor Events: A Retrospective Single-Center Study

Kim HJ, Jang HN, Ahn H, Yum MS, Ko TS

Purpose: Paroxysmal motor events are common clinical symptoms in infants visiting pediatric neurology clinics. Due to the heterogeneous clinical symptoms and the difficulty of interpreting electroencephalography (EEG) in infants, differentiating...
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Characteristics of Functional Speech Sound Disorders in Korean Children

Han MJ, Kim SJ

Purpose: A speech sound disorder (SSD) is defined as the presence of a problem with articulation and phonological processes in a child. This study analyzed the clinical characteristics of Korean...
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Usefulness of Magnetic Resonance Spectroscopy for the Initial Diagnosis of Mitochondrial DNA-Associated Leigh Syndrome

Na JH, Shin JH, Lee H, Lee YM

Purpose: Diagnosing Leigh syndrome (LS), a representative mitochondrial disease, remains challenging. Mitochondrial DNA (mtDNA)-associated LS, which is maternally inherited, has relatively well-known genetic variants. We evaluated the usefulness of brain...
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