- Usefulness of EEG in Children
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Eun BL
- KMID: 2335522
- J Korean Pediatr Soc.
- 2001 Apr;44(4):367-374.
No abstract available. -
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- A Case of Congenital Chylothorax in a Premature Infant
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Oh SK, Jeong YH, Choi YJ, Byun SO, Oh JS
- KMID: 2335534
- J Korean Pediatr Soc.
- 2001 Apr;44(4):460-463.
We experienced a case of isolated fetal pleural effusion diagnosed by antenatal ultrasonogram in the 33th week of gestational age. Chest PA at birth showed massive pleural effusion in both... -
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- A Case of Polyarteritis Nodosa in Childhood
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Seo JH, Kim DS, Kim MJ
- KMID: 2335533
- J Korean Pediatr Soc.
- 2001 Apr;44(4):456-459.
Polyarteritis nodosa(PAN) is a multisystemic disease primarily involving the small and medium- sized vessels. Prognosis depends on the presence and severity of visceral involvement. Gastrioin- testinal involvement in PQN may... -
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- Clinical Evaluation of Hypoglycemic Symptoms Reported by Children with Insulin-dependent Diabetes Mellitus and by Their Parents
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Lee BE, Park HY, Cheon CM, Kwon EK, Song SM, Kim JS, Jin DK
- KMID: 2335532
- J Korean Pediatr Soc.
- 2001 Apr;44(4):450-455.
PURPOSE: The following study has been carried out to find the symptoms of hypoglycemia and the symptoms of transient focal neurologic deficit, which were complained by insulin dependent diabetes mellitus... -
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- A Case of Acute Renal Failure Associated with Tsutsugamushi Disease
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Hong JH, Oho JH, Kim JH, Kho DK
- KMID: 2335535
- J Korean Pediatr Soc.
- 2001 Apr;44(4):464-468.
Tsutsugamushi disease is acute febrile illness, transmitted by Rickettsia tsutsugamushi. R. tsutusgamushi invade and proliferate in the endothelial cells of small blood vessels. Destruction of endothelial cells occurs from the... -
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- A Case of de novo Interstitial Deletion of 17 Chromosome
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Yoon KH, Lee HC, Kim AR, Kim KS, Pi SY, Seo EJ, Yoo HW
- KMID: 2335537
- J Korean Pediatr Soc.
- 2001 Apr;44(4):475-479.
This is the first reported case of a unique interstitial deletion involving the long arm of chromosome 17 in a Korean male infant born to parents with normal karyotype. The... -
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- A Case of Maple Syrup Urine Disease Associated with Acrodermatitis Enteropathica-like Syndrome Due to Iisoleucine Deficinecy During Diet Therapy
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Moon KH, Gwon OS, Lee JI, Rho SW, Jeon SS, Seo SS
- KMID: 2335536
- J Korean Pediatr Soc.
- 2001 Apr;44(4):469-474.
Maple syrup urine disease(MSUD) is an autosomal recessive disorder involving the metabolism of the branched-chain amino acids(BCAA) such as leucine, isoleucine and valine. The disorder is due to a defect... -
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- MMR Immunization Rate and Related Factors: Findings from Repeated Surveys (1996, 1999) on Elementary School Students in Kyonggi Province, Korea
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Ki M, Kim M, Shin YJ, Choi B
- KMID: 2335523
- J Korean Pediatr Soc.
- 2001 Apr;44(4):375-388.
PURPOSE: This study was carried out to obtain the immunization rate of MMR, and to know the related factors. METHODS: Subjects of the study were 3,364 students of 8 elementary schools... -
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- The Weaning Method of inhaled Nitric Oxide
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Lee HW, Lee JW, Hyun SY, Lee HC, Park CH, Park KY, Yoo HS, Lee KC, Jang YJ
- KMID: 2335527
- J Korean Pediatr Soc.
- 2001 Apr;44(4):413-417.
PURPOSE: inhaled nitric oxide(iNO) is an excellent method for the postoperative pulmonary hypertension in congenital heart disease. But more detailed care is needed because of the development of rebound pulmonary... -
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- The Effect of rhG-CSF and rhGM-CSF on Expression of Fc gamma Receptors and beta2 Integrin and Respiratory Burst Function in Human Granulocytes
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Kim KH, Ryu KH, Seoh JY
- KMID: 2335525
- J Korean Pediatr Soc.
- 2001 Apr;44(4):397-404.
PURPOSE: Receptors for the Fc of IgG(FcvR) and a beta2 integrin molecule, CD11c/CD18 are important in clearance of microbes by granulocytes. We performed an in vitro study on the effect... -
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- Antibody Levels and Opsonophagocytic Function to S. pneumoniae 19F Capsular Polysaccharide
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Kim KH, Seoh JY, Park MK
- KMID: 2335526
- J Korean Pediatr Soc.
- 2001 Apr;44(4):405-412.
PURPOSE: The increasing prominence of pneumococcal infections and of antimicrobial resistance has emphasized the need for a effective vaccine to reduce the risk of pneumococcal disease in childhood. To study... -
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- Ventricular Inhomogeneity and Beat-to-beat QT Interval Variability after Surgical Repair of Tetralogy of Fallot
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Kim SH, Yum MK, Kim NS, Kim CR, Lee CB, Noh CI, Kim HS
- KMID: 2335528
- J Korean Pediatr Soc.
- 2001 Apr;44(4):418-425.
PURPOSE: The object of this study is to determine whether QT interval variability in patients with postoperative tetralogy of Fallot increases. METHODS: We enrolled 41 patients who had total correction of... -
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- Significance between Ultrasonographic and Operative Findings in Hypertrophic Pyloric Stenosis
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Kim JH, Kim WT, Jung BO
- KMID: 2335529
- J Korean Pediatr Soc.
- 2001 Apr;44(4):426-432.
PURPOSE: The diagnosis of hypertrophic pyloric stenosis(HPS) can be made by clinical manifestations and upper gastrointestinal(UGI) series in most cases. Recently, the ultrasonogram(US) is a more accurate and reliable method... -
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- A Survey on the Factors of Breast Feeding Failure Related to the Role of Medical Personnels
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Cho MJ, Cheon CM, Seo JK, Shin SM
- KMID: 2335524
- J Korean Pediatr Soc.
- 2001 Apr;44(4):389-396.
PURPOSE: The reasons for breast feeding failure within the first month of birth were related to inappropriate handling of problems in breast feeding. We investigated common reasons for the failure... -
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- Expression of the NR2A and 2B Subunits of N-Methyl-D-aspartate Receptors in Hypoxic Neonatal Rat Hippocampus
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Lee JS, Lee DS, Park JH, Moon IS, Ko BH, Jung YW
- KMID: 2335530
- J Korean Pediatr Soc.
- 2001 Apr;44(4):433-442.
PURPOSE: The developing brain has been reported to be extremely susceptible to toxicity of ischemia and/or hypoxia during a restricted developmental period. Hippocampal neuronal cell death is a typical type... -
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- Clinical Characteristics of Williams Syndrome
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Shin CH, Kim HS, Yang SW, Choi JY
- KMID: 2335531
- J Korean Pediatr Soc.
- 2001 Apr;44(4):443-449.
PURPOSE: Williams syndrome(WS) is an autosomal dominant disorder resulting from a submicroscopic deletion of contiguous genes on the long arm of chromosome 7. We evaluated the physical, neurodevelopmental, and behavioral... -
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