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A case of Menkes disease with unusual hepatomegaly

Jeong GU, Cho A, Hwang H, Hwang YS, Kim KJ, Chae JH, Seo JK

Menkes disease is an X-linked recessive copper transport disorder characterized by neurological deterioration, connective-tissue damage, and abnormal hair growth. It is caused by the mutation of the ATP7A gene. This...
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Clinical Characteristics of Childhood Pompe Disease

Cho A, Jeong GU, Lim BC, Park JY, Moon JH, Chae JH, Hwang YS, Kim KJ, Hwang H

  • KMID: 1528185
  • J Korean Child Neurol Soc.
  • 2007 May;15(1):83-89.
PURPOSE: Pompe disease is one of the glycogen storage diseases caused by a deficiency of acid alpha-glycosidase. This enzyme defect results in lysosomal glycogen accumulation in many tissues and shows...
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Clinical Characteristics of Temporal Lobe Epilepsy in Childhood

Jeong GU, Cho AN, Lee JS, Park JY, Moon JH, Hwang H, Hwang YS, Kim KJ, Chae JH

  • KMID: 2329580
  • J Korean Child Neurol Soc.
  • 2006 Nov;14(2):276-285.
PURPOSE:Temporal lobe epilepsy(TLE) is now recognized as a distinct syndrome in adults. The seizure evolution in adult patients is well characterized, manifesting initially with an aura, behavioral arrest, automatism, and...
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Design and Management of Database Using Microsoft Access Program: Application in Neurointerventional Unit

Hwang SM, Jeong GU, Kim TI, Cha J, Pyun HW, Woo RC, Kim HS, Suh DC

PURPOSE: Complex clinical information in cerebral angiointervention unit requires effective management of statistical analysis for the classification of diagnosis and intervention including follow-up data from the interventional treatment. We present...
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