- A Case of Cyclosporine A: Induced Encephalopathy in a Child with Nephrotic Syndrome
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Bae EJ, Huh J, Lee HJ, Park WI, Lee KJ
- KMID: 2329242
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):342-346.
Cyclosporine A is the most frequently used immunosuppressive agent for prevention of graft versus host disease (GVHD) and treatment of frequently relapsing nephrotic syndrome in childhood. Some adverse effects such as hepatic... -
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- A Case of Facial Nerve Palsy Associated with Epstein-Barr Virus Infection in a Child
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Lee HK, Kim SB, Oh CH, Kim JW, Yun HS, Hwang SH, Song WK
- KMID: 2329241
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):337-341.
Facial palsy is a rare complication of infectious mononucleosis of Epstein-Barr virus infection, which can be easily overlooked by clinicians if one is unnoticed about it. We report a 2... -
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- A Case of Reye-like Syndrome Combined with Kawasaki Disease
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Park JH, Kim WS, Hahn YS, Park BS, Han HS
- KMID: 2329240
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):333-336.
Reye syndrome is characterized by an encephalopathy and fatty infiltration of the liver and other organs. Reye syndrome is usually associated with influenza B or varicella. Frequently these patients have been treated... -
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- A Case of Juvenile Onset Spinocerebellar Ataxia Type 3
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Kim JS, Kim YI, Lee KS, Jin DK
- KMID: 2329239
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):329-332.
The genetic locus of spinocerebellar ataxia type 3 (SCA3) is linked to chromosome 14q 24.3-qter like Machado-Joseph disease (MJD). The number of CAG repeats on mutant chromosome correlates positively with severity of... -
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- A Case of Spinocerebellar Ataxia Type 2
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Hong S, Lee GH, Yang DW, Lee W, Lee B, Kim JW
- KMID: 2329238
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):324-328.
This is a case of a boy with autosomal dominant cerebellar ataxia (SCA type 2), which was confirmed by DNA analysis. A 9-year-old boy had been suffering from tremor in both arm... -
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- A Case of Reflex Sympathetic Dystrophy Syndrome
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Jeong KJ, Choi BS, Kim BJ, Woo YJ, Ma JS
- KMID: 2329237
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):319-323.
Reflex sympathetic dystrophy syndrome (RSDS) is a well-recognized disorder in adult group. But it is rarely diagnosed in the pediatric age group. RSDS is often a response to a physical... -
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- A Case of Primary Antiphospholipid Syndrome with a Cerebrovascular Attack in a Child
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Kim SY, Lee IG, Choi BJ, Kim YH, Chung SY, Kim HK, Whang KT
- KMID: 2329236
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):309-313.
The antiphospholipid syndrome is a multisystemic disorder comprising of venous and arterial thrombotic events, recurrent unexplained fetal losses, moderate thrombocytopenia, and a high frequency of neurologic events with laboratory findings of a... -
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- MRI Diagnosis of Acute Disseminated Encephalomyelitis (ADEM): Clinical Characteristics Based on the Lesion of Distribution
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Lee SJ, Lee R, Kim SK, Lee IK, Chae JH, Kim KJ, Hwang YS, Kim IO
- KMID: 2329235
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):297-302.
PURPOSE: Acute disseminated encephalomyelitis (ADEM) is a demyelinating disease of the central nervous system preceded by viral illnesses or vaccinations. Diagnosis depends on the clinical manifestations and the neuroimaging findings. The authors... -
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- A Study of The Relationship Between Headache and Depressive Trends in Elementary School Children
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Rho YI, Moon GR, Park YB, Yang ES, Park SK, Kim EY, Park J
- KMID: 2329234
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):288-296.
PURPOSE: The purpose of our study is to determine the relationship between the level of depression and characteristics of headache in elementary school children. METHODS: A self-administered questionnaire was completed by one... -
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- The Diagnostic Significance of Clinical Characteristics and Neuroimaging Findings for Diagnosis of Children with Developmental Delay
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Oh KS
- KMID: 2329233
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):272-287.
PURPOSE: In order to identify developmental disability and help the patients earlier, the diagnostic significance of clinical characteristics and neuroimaging findings for diagnosis of children with developmental delay was studied. METHODS:... -
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- The Clinical Manifestations and Results of Medical and Surgical Treatment of Epileptic Children with Neuronal Migration Disorders
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Eun SH, Chung SH, Lee M, Joo CU, Cho SC, Kim S
- KMID: 2329232
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):264-271.
PURPOSE: The objective of this study is to investige the clinical features, natural histories, and results of medical and surgical treatment of NMD in patients who were diagnosed during childhood. METHODS: We... -
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- Clinical Manifestations and EEG Findings of Children with Centro-temporal Spikes
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Cho KH
- KMID: 2329231
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):257-263.
PURPOSE: The objective of this study is to review the clinical manifestations and EEG findings of children with centro-temporal spikes. METHODS: We reviewed the clinical records of 38 patients showed epileptiform discharges on... -
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- Clinical and Electrographic Characteristics of Intractable Childhood Epilepsy with Complete Seizure Remission Over 6 Months After Ketogenic Diet
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Kim YR, Kim HD
- KMID: 2329230
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):242-249.
PURPOSE: The efficacy of ketogenic diet in intractable childhood epilepsy has been reported in Korea. The aim of this retrospective study is to elicit the clinical and electrophysiological characteristics of intractable chilhood... -
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- Changes of c-Fos Immunoreactivity in Rat Brain Neurons According to Ages After Induced Pain
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Park YC, Yoo KS, Hawan GK
- KMID: 2329229
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):231-241.
PURPOSE: The pathways of pain conduction in brain are not well known. Also, differences of somatic pain conduction between adult and young age have not been fully elucidated. This study was conducted... -
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- Mutation Analysis of the Dystrophin Gene by Application of PCR in Duchenne Muscular Dystrophy
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Han SK, Kim JW, Son BK, Chae JH, Hwang YS
- KMID: 2329228
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):221-230.
PURPOSE: Large rearrangements in the dystrophin gene is detected in about 65-70% of patients by multiplex PCR or Southern blot, although detection of point mutations and microlesions is currently in progress. The... -
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- Diagnosis of Duchenne/Becker Muscular Dystrophy: Clinical and Moleculargenetic Characteristics
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Lee JH, Chae JH, Kim KJ, Joo S, Park S, Cho HI, Chi JG, Hwang YS
- KMID: 2329227
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):211-220.
PURPOSE: Duchenne/Becker muscular dystrophy (DMD/BMD) is an X-linked recessive disease caused by the mutation of dystrophin gene. Since the majority of mutations are deletions, recent diagnosis is made by the moleculargenetic tools.... -
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- The DiI Staining of Interneuron Dendrites in Kainate-Treated Hippocampal Slice Culture
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Kim YH, Lee IG, Chung SY, Whang KT
- KMID: 2329226
- J Korean Child Neurol Soc.
- 2000 Dec;8(2):204-210.
PURPOSE: Excitotoxic injury of the dendrites of inhibitory interneurons could lead to decrease in their synaptic activation, and explain subsequent local circuit hyperexcitability and epilepsy. A hallmark of dendrotoxicity at least in... -
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