- Utility Change of Health Care Services after Separation of Dispensary from Medical Practice
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Lee KD
- KMID: 2207347
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1095-1102.
No abstract available. -
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- Electrophysiologic Study of Cardiac Conduction System in Children
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Shin CO, Hyun MC
- KMID: 2207352
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1135-1140.
PURPOSE: Pediatric cardiac arrhythmias are increasing but there is no normal values of cardiac electrophysiologic studies(EPS) in Korean children. So we performed cardiac EPS in children undergoing cardiac catheterization for... -
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- A Case of Menetrier's Disease Associated with Cytomegalovirus Infection
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Cho JR, Kang SK, Kim YH, Choe YH
- KMID: 2207361
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1197-1200.
We report the case of a 4 year-old boy with Menetrier's disease, who was presented with edema and hypoalbuminemia. Gastroduodenal endoscopy showed the characteristic features of giant hypertrophy of the... -
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- A Case of Annular Pancreas and Endocardial Cushion in the Abscence of Down Syndrome
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Cho HJ, Yu JJ, Lee YR, Moon C
- KMID: 2207360
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1193-1196.
Annular pancreas is a rarely found gastrointestinal tract malformation, and is frequently associated with Down syndrome. Endocardial cushion defect is a type of congenital heart disease, commonly also related to... -
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- Nitroblue Tetrazolium(NBT) Test as a Screening Test of Urinary Tract Infection in Children
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Huh N, Oh CH, Kim JW, Oh PS, Yoon HS, Song WK
- KMID: 2207354
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1157-1161.
PURPOSE: It has been reported that the Nitroblue Tetrazolium(NBT) test is more accurate than the urine pH, leukocyte esterase and nitrite test as a screening test of urinary tract infection... -
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- Nonrhizomelic Type of Chondrodysplasia Punctata Suspected in the Brothers
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Kim JS, Jung HS, Kim YS, Park CH, Choi MB, Woo HO, Youn HS
- KMID: 2207359
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1187-1192.
Chondrodysplasia punctata is a heterogenous skeletal dysplasia characterized by small focal calcifications in articular and other cartilages in infancy, with subsequent epiphysial dysplasia and associated anomalies of the face, eyes,... -
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- A Case of Nemaline Myopathy
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Kim BJ, Choi IJ, Kim DS, Nam SO
- KMID: 2207358
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1182-1186.
Childhood onset nemaline myopathy, first described in 1963 by Shy, et al and Conen, et al, is rare congenital myopathy, characterized by nonprogressive or slowly progressive muscle weakness associated with... -
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- Fanconi-Bickel Syndrome Presented with Diabetes Mellitus and Galactosemia : Identification of a Novel Mutation in the GLUT2 Gene
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Kim YJ, Rim SH, Shin YL, Yoo HW
- KMID: 2207362
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1201-1205.
Fanconi-Bickel syndrome is a rare autosomal recessive disorder of the carbohydrate metabolism recently demonstrated to be caused by mutations in GLUT2, the gene for the glucose transporter protein 2 expressed... -
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- Evoked Potentials and Cranial Ultrasonography as a Prognostic Method in Newborn with Asphyxia
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Kim HJ, Kang H, Choi BM, Yoo KH, Lee JW, Kim SK
- KMID: 2207355
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1162-1167.
PURPOSE: This study was aimed at finding a diagnostic tool which is useful in predicting the neurologic outcome of the asphyxiated newborns. METHODS: 31 newborns with asphyxia were evaluated by brainstem... -
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- Two Cases of HHH Syndrome in Siblings
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Hwang MH, Kim BS, Lee DH
- KMID: 2207363
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1206-1210.
Hyperornithinemia-hyperammonemia-homocitrullinuria(HHH) syndrome is a rare autosomal recessive disorder caused by a defect in the urea cycle. Protein intolerance, mental retardation, seizure, ataxia, and stupor are characteristic symptoms. Patients showing these... -
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- A Congenital Cutis Laxa Fatality Caused by Early Onset Pulmonary Emphysema
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Lee TW, Seong SJ, Jeung YM, Kim JB, Kim ER, Yoon YS
- KMID: 2207357
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1176-1181.
Cutis laxa is a rare disorder of the elastic tissue characterized by loosely hanging and folded skin giving a premature senile appearance, often with internal organ involvement. Recently, we experienced... -
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- A Study on the Disease Course and Prognosis of Cyclic Vomiting Syndrome
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Yang HR, Ko JS, Seo JK
- KMID: 2207353
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1141-1156.
PURPOSE: To describe clinical features of cyclic vomiting syndrome(CVS), managements during episodes, prophylactic drugs as long term therapy and to investigate the disease course and prognostic factors of CVS. METHODS: Thirty... -
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- Clinical Efficacy of Selective Fetal Echocardiography
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Hong SY, Ban JE, Lee YS, Lee HD
- KMID: 2207351
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1127-1134.
PURPOSE: The aims of this study was to assess the indication, diagnostic, accuracy and prognostic influence of fetal echocardiography. METHODS: From 1995 to 1999, 283 pregnancies were evaluated with fetal echocardiography... -
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- Relationship between Serum Leptin Levels and Other Predictors in Obese Children
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Park SJ, Park KW, Hong YM
- KMID: 2207348
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1103-1111.
PURPOSE: The product of the ob gene, leptin is an adipocyte specific hormone that might be involved in the regulation of food intake by the central neuroendocrine system. Recent studies... -
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- The Relationship of Maternal Disorder with Neonatal Cord Blood Leptin - Preeclampsia, Diabetes Mellitus, Antenatal Steroid Treatment -
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Park SM, Kim EY, Park YB, Park SK
- KMID: 2207350
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1119-1126.
PURPOSE: Leptin, the product of the ob gene is primarily by adipose tissue but also by the human placenta. Leptin may also have a role as a regulator of fetal... -
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- Growth and Neurodevelopmental Outcome at 15 Months of Corrected Age in Very Low Birth Weight Infants with Chronic Lung Disease
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Kim SY, Cho CY, Choi YY
- KMID: 2207349
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1112-1118.
PURPOSE: This study was performed to compare the growth and neurodevelopmental outcome at 15 months of corrected age in very-low-birth weight infants between chronic lung disease(CLD) group and the control... -
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- Serum Level of G-CSF and GM-CSF and CFU-GM Response to Hematopoietic Growth Factors in a Patient with Cyclic Neutropenia
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Lee YK, Kim SH, Kim KW, Lee S, Kim HS, Chun DS, Lee KS
- KMID: 2207356
- J Korean Pediatr Soc.
- 2001 Oct;44(10):1168-1175.
PURPOSE: Serum levels of G-CSF and GM-CSF were measured and CFU-GM assay using G- CSF, GM-CSF and SCF was conducted to evaluate the influence of hematopoietic growth factor on the... -
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