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An Indian Family with Childhood Onset of Striatal Necrosis

Nagabushana D, Srikanteswara PK, Netto A, Nagaraj K

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KCNQ2-Related Benign Infantile Epilepsy in Preterm Dizygotic Twins

Kwon CM, Lee KH

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Orbital Myositis Mimicking Status Migrainosus

Kim YJ, Yoo IH

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Aseptic Zoster Meningoencephalitis with Ophthalmic Shingles in an Immunocompetent 3-Year-Old Boy

Jeong H, Rhie S, Chae KY

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Stroke-Like Episodes Associated with Coronavirus Disease 2019 in a Child with MELAS Syndrome

Kim WJ, Yum MS, Kim MJ, Jang HN, Ko TS

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A Case of Mitochondrial Trifunctional Protein Deficiency with HADHB Variants Diagnosed Using Whole-Exome Sequencing

Kim C, Lee D, Lee J, Cho SY, Lee J

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Robot-Assisted Stereoelectroencephalography for Pediatric Epilepsy Surgery: The First Case in Korea

Cho K, Chang WS, Kim HD, Chang JW, Kim SH, Lee JS, Kang HC

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Isolated Unilateral Hypoglossal Nerve Palsy Associated with Influenza B Virus Infection in a Child

Park IB, Youn SE

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Split-Hand/Foot Malformation and Subependymal Heterotopia Caused by a DLX5 Gene Mutation: A Case Report

Shin JH, Han MJ, Kim SJ

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Effects of Occipital Nerve Block in Pediatric Patients with Occipital Region Headache

Son HJ, Lee KH

Purpose: The aim of this study was to investigate the effects of occipital nerve block (ONB) in pediatric patients with headache in the occipital region. Methods: Among 302 patients who visited...
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The Value of High-Resolution Vessel Wall Magnetic Resonance Imaging in the Diagnosis and Management of Primary Angiitis of the Central Nervous System in Children

Sung J, Lee D, Song JY, Lee J, Kim JH, Lee J

Purpose: High-resolution vessel wall-magnetic resonance imaging (VW-MRI) has been used to detect regional vessel wall pathology, significantly contributing to the diagnosis of primary angiitis of the central nervous system (PACNS)...
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Heterogeneous Clinical Characteristics of Allan-Herndon-Dudley Syndrome with SLC16A2 Mutations

Han JY, Lee S, Woo H, Kim SY, Kim H, Lim BC, Hwang H, Choi J, Kim KJ, Chae JH

Purpose: The purpose of this study was to expand our understanding of phenotypic and genetic variation in Allan-Herndon-Dudley syndrome (AHDS), which is a rare X-linked mental retardation syndrome characterized by...
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