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Identification of a Novel Mutation in the ATP7A Gene in a Korean Patient with Menkes Disease

Kim YH, Lee R, Yoo HW, Yum MS, Bae SH, Chung SC, Park YM, Son JS

Menkes disease is an infantile-onset X-linked recessive neurodegenerative disorder caused by diverse mutations in a copper-transport gene, ATP7A. Affected patients are characterized by progressive hypotonia, seizures, failure to thrive and...
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Psychological Problems and Clinical Outcomes of Children with Psychogenic Non-Epileptic Seizures

Yi YY, Kim HD, Lee JS, Cheon KA, Kang HC

PURPOSE: Our purpose was to investigate psychological problems and clinical outcomes in children with psychogenic non-epileptic seizures (PNES). MATERIALS AND METHODS: We retrospectively reviewed the data of 25 patients who were...
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Magnetoencephalography in Pediatric Lesional Epilepsy Surgery

Kim H, Lim BC, Jeong W, Kim JS, Chae JH, Kim KJ, Chung CK, Hwang YS, Hwang H

This study was performed to assess the usefulness of magnetoencephalography (MEG) as a presurgical evaluation modality in Korean pediatric patients with lesional localization-related epilepsy. The medical records and MEG findings...
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