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Asymptomatic Fracture of a Distal Shunt Catheter after Ventriculoperitoneal Shunt for Post-traumatic Hydrocephalus

Seung WB, Park YS

  • KMID: 2043933
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):33-38.
A fracture of a distal shunt catheter is a rare complication. In many cases of shunt failure, shunt revision should be performed to prevent the development of hydrocephalus. However, the...
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A Case of Cri du Chat Syndrome with Developmental Delay Misdiagnosed as Fetal Alcohol Syndrome

No SJ, Kim DO, Lee SM, Lee JS

  • KMID: 2043931
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):23-27.
Cri du Chat syndrome (CdCS) is a chromosomal disease resulting from a deletion on the short arm of chromosome 5. Characteristic features include high pitched cat-like cry, distinguishing facial features,...
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A Case of Cervical Disc Herniation with Paresthesia in Both Arms and Tic Mimicking Motions

O HL, Moon JH, Seol IJ, Yum MK, Park DW

  • KMID: 2043935
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):43-47.
Intervertebral disc herniation is rare in children and is reportedly related with disc calcification and traumatic injury. We report an 8 years old girl, who complained of tingling sensation in...
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Intracranial Neurenteric Cyst of the Anterior Brain Stem in a Girl

Lee CW, Lee SH, Yu ST

  • KMID: 2043930
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):18-22.
Neurenteric cyst is a rare, congenital, and benign cystic lesion of the central nervous system, which is generally thought to result from failure of separation of the neuro-ectodermal and neuro-endodermal...
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Atypical Miller-Fisher Syndrome Presenting as an Isolated Internal Ophthalmoplegia Following Epstein-Barr Virus Infection

Park HJ, Lee KH

  • KMID: 2043934
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):39-42.
Acute external ophthalmoplegia, areflexia, and ataxia compose the classic Miller-Fisher syndrome (MFS). Pupillary dysfunction is present in half of patients with MFS. However, isolated internal ophthalmoplegia is rare in children...
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An Arg528His Mutation of the CACNL1A3 Gene in a Korean Family with Hypokalemic Periodic Paralysis

Kim KR, Suh ES, Lee YM

  • KMID: 2043932
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):28-32.
Familial hypokalemic periodic paralysis (HOPP) is an autosomal dominant disorder characterized by episodic attacks of muscle weakness with concomitant hypokalemia (
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A Correlation Analysis between Febrile Seizures and Viral Infections

Lee SJ, Kim JM, Park HJ

  • KMID: 2043929
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):9-17.
PURPOSE: Viral infections are common in children,. This study was aimed to identify the correlation between febrile seizures and virus infections, to reduce the use of antibiotics and to help...
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The Comparative Analysis of Bacterial and Aseptic Meningitis in Neonates

Cho SD, Kang B, Park SH, Sung HU, Jun YH, Hong YJ, Son BK, Kwon YS

  • KMID: 2043928
  • J Korean Child Neurol Soc.
  • 2012 Mar;20(1):1-8.
PURPOSE: This study was aimed to evaluate the clinical features of bacterial and aseptic meningitis in neonates. METHODS: Seventy seven neonates who diagnosed with meningitis at Inha University Hospital from June...
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