Skip Navigation
Skip to contents
Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

18 results
Display

A Case of Intracranial Lipoma

Yun JM, Jo EY, Lim JW, Choen EJ, Ko KO, Lee YH

  • KMID: 2177023
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):114-118.
Intracranial lipomas are rare lesions, which represent 0.1-1.7% of all intracranial tumors. They preferentially occur near the midline, most frequently in the pericallosal cistern, and are often associated with various...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Valproic Acid Associated with Acute Pancreatitis

Lee EH, Yi YJ, Park HJ

  • KMID: 2177015
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):69-73.
Valproic acid is a commonly prescribed medication approved for epilepsy, migraine and bipolar disorder. The common adverse effects associated with valproic acid include nausea, vomiting, tremor and weight gain. Less...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Epilepsy, Reactive Oxygen Species and Mitochondria

Kim WS

  • KMID: 2177006
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):1-7.
Epilepsy is a neurological disorder from many molecular and biochemical responses. In the underlying mechanism, reactive oxygen species play an important role in seizure initiation and seizure-induced brain damage. In...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
One Case of Childhood Adrenoleukodystrophy Involving the White Matter of the Frontal Lobe

Lee HS, Kang HC

  • KMID: 2177021
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):104-108.
Childhood adrenoleukodystrophy is a progressive, demyelinating disease of the white matter. Although it is sometimes misdiagnosed as a psychiatric disorder, it can be reliably confirmed by magnetic resonance imaging(MRI) and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Reversible Posterior Leukoencephalopathy Involving in the Spinal Cord with Pheochromocytoma

Lee SW, Hong SY, Lee YS, Choi SS, Hwang KG

  • KMID: 2177022
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):109-113.
Reversible posterior leukoencephalopathy with hypertension is characterized by an acute and severe rise in blood pressure with headache, altered mental status, cortical visual disturbance, seizure and transient edematous changes in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Comparative Study between Bayley Scales of Infant Development-II and Korean Infant and Child Developmental Test in Infants Younger than 12 Months

Kim SG, Kim NC, Lee IK, Oh MH, Kim YC, Lee HJ

  • KMID: 2177012
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):48-56.
PURPOSE: Currently, there are many developmental tests of scale and screening for infants and children. However, it has been questioned about the discriminating power and the correlation among developmental tests...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Chronic Inflammatory Demyelinating Polyradiculoneuropathy Associated with Perianal Abscess by Klebsiella pneumoniae

Lee YS, Kim SY, Kim YJ, Lee EJ

  • KMID: 2177019
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):94-98.
Chronic inflammatory demyelinating polyradiculoneuropathy(CIDP) is a rare acquired demyelinating disease of peripheral nervous system(PNS), characterized by relapsing or progressive proximal and distal muscle weakness with possible sensory loss. It is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Isolated Interhemisphere Fusion of Frontal Lobe with Intact Septum Pellucidum : A Variant of Holoprosencephaly

Kim SW, Kim MS, Park JR, Yoo HJ, Kim CH, Lee HH, Park RH

  • KMID: 2177017
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):79-83.
Holoprosencephaly is a rare CNS developmental defect with midline cleavage of embryonal forebrain during the fourth week of fetal development characterized with s single ventricle. Holoprosencephaly is divided into three...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two Cases of Influenza-associated Encephalopathy

Park MK, Lee IK, Oh MH, Kim YC, Kim Y

  • KMID: 2177018
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):84-93.
Influenza-associated encephalopathy is typically associated with a sudden onset of high fever, severe convulsions, rapidly progressive coma and death within 2 or 3 days. It has been actively researched in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of a Coincidence of Rolandic and Childhood Absence Epilepsy

Song YH, Jun YS, Choi SR, Lee SY, Jeong DC, Kang JH, Chung SY

  • KMID: 2177016
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):74-78.
Rolandic epilepsy(or benign epilepsy with centrotemporal spikes) and childhood absence epilepsy are idiopathic epilepsies and are the most common forms of age-related epilepsies, occurring in previously neurologically normal children. Benign...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Bicuculline Induced Epileptiform Activity

Choi BJ

  • KMID: 2177013
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):57-62.
PURPOSE: The goal of this study was to investigate the effects of bicuculline(BIC) on the excitability of visual cortex, observe the induction of epileptiform activity and define the characteristics of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Investigation of Benign Afebrile Seizure with Gastroenteritis

Lee EH, Choi DY, Park HJ

  • KMID: 2177009
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):23-30.
PURPOSE: The aim of this study is to characterize detailed clinical features of benign afebrile seizure with gastroenteritis. METHODS: We retrospectively investigated the medical records of 52 patients with benign afebrile...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Study of Priority between Prognostic Factors of Status Epilepticus in Childhood

Lee SE, Kim HS, Yoo HJ

  • KMID: 2177008
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):15-22.
PURPOSE: Poor prognostic factors of status epilepticus(SE) in children have been known as less than 1 year of age, generalized tonic clonic type of convulsion, symptomatic etiology, and duration of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Vagus Nerve Stimulation In Intractable Pediatric Epilepsy Patients

You SJ, Kim DS, Lee JK, Ko TS

  • KMID: 2177007
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):8-14.
PURPOSE: We intended to evaluate the efficacy, safety, and effects on quality of life of vagus nerve stimulation(VNS) in children with intractable epilepsy. METHODS: We retrospectively studied the medical records...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Brain Magnetic Resonance Imaging in Children with CNS Manifestations

Shin MS, Park KS, Kim YD, Song CJ, Lee KS

  • KMID: 2177011
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):41-47.
PURPOSE: This study is to examine the relationship between clinical manifestations and MRI findings of children with CNS symptoms and signs. METHODS: A total of 447 inpatients with CNS symptoms and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
4 Aminopyridine Induced Epileptiform Activity

Choi BJ, Whang KT

  • KMID: 2177014
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):63-68.
PURPOSE: The goal of the present study was to investigate the effects of 4-aminopyridine(4-AP) on the excitability of visual cortex, observe the induction of epileptiform activity and define the characteristics...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Neonatal Adrenoleukodystrophy Presented with Neonatal Seizure

Choi J, You SJ, Ko TS, Kim EA, Kim KS, Pi SY, Yoo HW

  • KMID: 2177020
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):99-103.
Neonatal adrenoleukodystrophy(NALD) is an inherited autosomal recessive disease characterized by very early onset of neurologic deterioration, extreme hypotonia, poor sucking reflex, failure to thrive, poor or absent grasp and Moro...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Merosin Deficient Congenital Muscular Dystrophy in Korea

Lee JS, Kim HM, Kim SH, Park SY, Lee JH, Chae JH, Kim KJ, Hwang YS, Kim IO, Choi GY

  • KMID: 2177010
  • J Korean Child Neurol Soc.
  • 2005 May;13(1):31-40.
PURPOSES:Congenital muscular dystrophies(CMDs) are an autosomal recessive and heterogeneous disorders. The classic forms of CMD are subclassified into two major categories:merosin positive and deficient. Merosin deficient congenital muscualr dystrophy (MDCMD)...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr