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Novel Mutation in the CACNA1B Gene Linked to Pediatric Focal Epilepsy

Lyu JH, Shin HJ, Lee JS, Kang HC

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Unveiling the Uncommon: A Case of Postoperative Inflammatory Sciatic Neuropathy in a Child

Singh R, Peer S, Bali A, Gupta V, Wander A

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A Surfer’s Myelopathy in a 7-Year-Old Boy after His First Time Surfing

Jang J, Kim HJ, Kim MJ, Yum MS, Ko TS

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A Rare Pediatric Case of Top of the Basilar Syndrome

Lee JY, Lee HJ, Byun JC

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Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay (CLIFAHDD) Associated with a De Novo Missense Variant in NALCN: The First Korean Case Report

Jo YH, Lee YJ, Kong J, Lee YJ, Nam SO, Kim YM

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Identification of De Novo Radio-Tartaglia Syndrome and Comparison of Clinical and Molecular Characteristics with Those of 1p36 Deletion Syndrome

Kim HY, Lee J, Jang JH, Kim JW, Lee J, Jang MA

Purpose: Radio-Tartaglia syndrome (RTS; Mendelian Inheritance in Man [MIM]: 619312) is a rare neurodevelopmental disorder with few reported cases and limited research. It has recently been reported that the clinical...
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Prolonged-Release Melatonin for Sleep Disturbances in Autism Spectrum Disorder

Vivas EA, Ron AG, Alguacil EG, Gascón MB, de Santos Moreno MT, Cabrera ES, de las Cuevas GRO, Peñas JJG, Hoyo RSd, Insuga VS

Purpose: Patients with autism spectrum disorder (ASD) often present with sleep disturbances. We evaluated the effectiveness of pediatric prolonged-release melatonin (PedPRM) in real clinical practice, focusing on a population of...
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