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A Case of Malignant Transformation of Juvenile Pilocytic Astrocytoma with Neurofibromatosis Type 1

Eom KS, Choi KH, Kim TY

  • KMID: 2329496
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):292-297.
Pilocytic astrocytoma (PA) is a World Health Organization (WHO) grade I tumor typically affecting children and young adults. In general, surgical resection for PA is thought to be curative, and...
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A Case of a Human Tail Without Associated Anomalies

Kang B, Oh SK, Son BK, Kwon YS, Lim MK, Choi YM, Choi SJ

  • KMID: 2329495
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):287-291.
Human tails or caudal cutaneous appendages are rare congenital anomalies with lesions usually arising from the midline of the lumbosacrococcygeal area. There have been only around 70 cases reported in...
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A Case of Acute Encephalopathy Associated with Non-typhoidal Salmonellosis

Han YH, Lee KH

  • KMID: 2329494
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):283-286.
Non-typhoidal salmonella (NTS) is a common pathogen involved in food poisoning. It has various extraintestinal complications including encephalopathy. However, NTS associated encephalopathy is rarely reported. A previously healthy 14-year-old boy...
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A Case of Brainstem Encephalitis Associated with Epstein-Barr Virus Infection

Oh MJ, Lim SJ, Kim YJ, Eom TH, Lee HS, Jang PS, Kim YH

  • KMID: 2329493
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):277-282.
A case of brainstem encephalitis associated with a reactivated infection of Epstein-Barr virus (EBV) in a 7-year-old boy is reported. The patient was diagnosed based on the compatible clinical, cerebrospinal...
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A Case of Metachromatic Leukodystrophy Confirmed by Molecular Genetic Analysis

Lee JH, Min KB, Lee YM, Kang HC, Lee JS, Kim HD

  • KMID: 2329492
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):272-276.
Metachromatic leukodystrophy (MLD) is the rare neurometabolic disease caused by the deficiency of the enzyme arylsulfatase A resulting in a deficiency of sulfatide degradation and the target gene is ARSA...
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A Case of Early Onset MELAS Patient with Wolff-Parkinson-White Syndrome

Kim JA, Ahn JM, Lee YM, Kang HC, Lee JS, Kim HD

  • KMID: 2329491
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):266-271.
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is one of the classic mitochondrial diseases characterized by symptoms of repeated episodes of hemiparesis with mitochondrial DNA mutation. We report...
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Successful Desensitization of Oxcarbazepine: First Case in Pediatric Patient

Lee OJ, Yu HJ, Lee CG, Nam SH, Lee BL, Lee J, Lee M

  • KMID: 2329490
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):262-265.
Aromatic antiepileptic drugs (AEDs), such as diphenylhydantoin, phenobarbital, or carbamazepine (CBZ), are frequently associated with hypersensitivity reactions. This may restrict treatment options considerably due to cross reactivity with other aromatic...
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A Case of the Hirayama Disease in Young Male Adolescent

Yeom JS, Cho JY, Lim JY, Park CH, Woo HO, Youn HS, Park KJ, Kwak B, Kim YS

  • KMID: 2329489
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):257-261.
In the present study, we report muscular atrophy of the right distal upper extremity in a 14-year-old boy. The disease progressed insidiously for about 2 years, and during our first...
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Clinical Analysis of Restless Legs Syndrome in Korean Children

Seo H, Kim S, Kwon S

  • KMID: 2329488
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):249-256.
PURPOSE: Restless legs syndrome (RLS) is a common neurologic sleep disorder, but it is frequently undiagnosed in Korean children. This study aimed to investigate clinical features of RLS in Korean...
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The Early Clinical Manifestations and Prognostic Factors of Juvenile Dermatomyositis

Lee G, Lee JH, Nam SH, Lee BL, Lee J, Lee M

  • KMID: 2329487
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):240-248.
PURPOSE: Juvenile dermatomyositis (JDM) is a common inflammatory myopathy in childhood. However, the diagnosis is often delayed because it frequently present with non-specific symptoms. In addition, there are conflicting opinions...
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A1 Segment Hypoplasia/aplasia Detected by Magnetic Resonance Angiography in Neuropediatric Patients

Han YK, Kim S, Yoon CS, Lee YM, Kang HC, Lee JS, Kim HD

  • KMID: 2329486
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):231-239.
PURPOSE: A variation in the circle of Willis is not so common, but the most frequent type is hypoplasia/aplasia of the precommunicating anterior cerebral arteries (A1 segment). We aimed to...
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Effect of Gestational Exposure to Bisphenol A on Neuronal Stem Cell Differentiation in the Neonatal Rat Hippocampus

Wang SW, Kim JM, Hwang KG

  • KMID: 2329485
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):218-230.
PURPOSE: Neurogenesis in neonatal period after birth occurs consequently through a series of neuronal stem/progenitor cell proliferation and differentiation. This stage is critical for determining of normal development and maturation...
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Clinical Features and Prognostic Factors of Neurologic Outcome in Group B Streptococcal Meningitis

Cho HL, Shin HW, Kim KS, Kim EY

  • KMID: 2329484
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):208-217.
PURPOSE: Group B streptococcal (GBS) meningitis is the leading cause of mortality and morbidity in neonates. There are limited current data regarding outcomes from GBS meningitis and factors that predict...
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Analysis of Urine Iodine Concentration by Inductively Coupled Plasma-mass Spectrometry Method in Normally Developed Children Aged Less than 7 Years in Masan City (Korea)

Lee JH

  • KMID: 2329483
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):199-207.
PURPOSE: Iodine is an essential component of thyroid hormones, and iodine deficiency disorder, including mental retardation, hypothyroidism, goiter, cretinism, and developmental abnormalities is the world's greatest single cause of preventable...
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Neurologic Manifestations and Prognosis in Hemophagocytic Lymphohistiocytosis

Ryu HW, Doo KH, Kim SS, Lim BC, Hwang H, Kim KJ, Hwang YS, Chae JH

  • KMID: 2329482
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):191-198.
PURPOSE: Hemophagocytic lymphohistiocytosis (HLH) presenting with neurologic manifestationhas a poor prognosis due to delayed diagnosis and treatment. We investigated the time between onset of symptoms and diagnosis of HLH and...
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Bone Mineral Density in Ambulatory Epileptic Children with New Antiepileptic Drug Monotherapy

Ko JH, Lee GM, Lee EH, Chung S

  • KMID: 2329481
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):184-190.
PURPOSE: This study was conducted for evaluation of the effects of new antiepileptic drugs on bone mineral density in children with epilepsy. METHODS: The study group consisted of 35 age and...
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Amplitude Integrated Electroencephalography in the Neonatal Intensive Care Unit for Diagnosis of Neonatal Seizure

Kim YJ, Sim GY, Kim MJ, Lim G, Kim WS

  • KMID: 2329480
  • J Korean Child Neurol Soc.
  • 2011 Dec;19(3):177-183.
PURPOSE: To assess the usefulness of amplitude integrated electroencephalography (aEEG), we compared aEEG with electroencephalography (EEG), which is one of the most useful tools for assessment of neonatal seizures in...
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