- A Case of C1q Nephropathy in Steroid-Dependent Nephrotic Syndrome
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Lee JW, Cho SJ, Lee SJ, Sung SH
- KMID: 2144707
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):206-209.
C1q nephropathy is an immune complex glomerulonephritis defined by the presence of mesangial C1q deposits in immunofluorescence microscopy and electron dense deposits on electron microscopy. It was described as a... -
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- A Case of Rhematogenous Retinal Detachment in Children with Nephrotic Syndrome during Systemic Corticosteroid Therapy
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Kim JY, Kim JH, Cho BS, Yu SY, Kwak HW
- KMID: 2144708
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):210-212.
Retinal detachment is a rare disease in children but cases of serous retinal detachment due to use of systemic corticosteroids have been reported in and out country. Rhematogenous retinal detachment... -
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- A Case of Multilocular Cystic Nephroma in Childhood
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Choi MS, Lee YM, Kim JH, Kim PK, Jeong HJ, Kim MJ
- KMID: 2144711
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):225-230.
Multilocular cystic nephroma is a rare disease, noninherited benign renal neoplasm occurring in both children and adults. It is necessary to make a differential diagnosis from all renal diseases with... -
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- A Case of Lupus Nephritis with Positive Antiphospholipid Antibodies, Initially Detected Through Analysis of Urinary Mass Screening
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Lee TJ, Choi MS, Lee YM, Kim JH, Kim PK, Jeong HJ
- KMID: 2144710
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):219-224.
Antiphospholipid syndrome is a thrombotic disorder characterized by the association of arterial and venous thrombosis with the antibodies directed toward phospholipids. The presence of these antibodies in systemic lupus... -
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- Clinical Significance of Mild Fetal Pelviectasia and The Role of Postnatal Voiding Cystourethrography
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Park S, Kim SH, Yoo ES, Park EA, Lee SJ
- KMID: 2144704
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):182-187.
PURPOSE: To evaluate the clinical significance of antenatally detected mild fetal pelviectasia and the role of voiding cystourethrography (VCUG). METHODS: From January 1999 to September 1999, 28 neonates (44 pelviectatic kidneys)... -
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- Membranous Glomerulopathy Showing Asymptomatic Isolated Microscopic Hematuria Only
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Kim SH, Roh HK, Lee YM, Kim JH, Kim PK, Hong SW, Jeong HJ
- KMID: 2144706
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):196-205.
PURPOSE: Membranous glomerulopathy is a glomerular disease characterized by the presence of subepithelial immune deposits with thickening of the capillary wall of the glomerulus without inflammatory change. The pathogenesis of... -
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- Evaluation of Timing of Voiding Cystourethrogram after Urinary Tract Infection
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Lee JA, Choi JE, Kim SM, Jung JH
- KMID: 2144703
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):176-181.
PURPOSE: Urinary tract infection is a common problem in children. To evaluate for reflux most authorities recommend a voiding cystourethrogram 3 to 6 weeks after the first urinary tract infection.... -
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- Long-term Prognostic Factors in Pediatric Focal Segmental Glomerulosclerosis
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Kim EA, Lee YM, Kim JH, Lee JS, Kim PK, Jung HJ
- KMID: 2144698
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):125-135.
PURPOSE: Efforts to predict long-term outcome of focal segmental glomerulosclerosis(FSGS) have been made but have yielded conflicting results. Reports are rare especially in pediatric patients. In this study, we reviewed... -
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- A Case of Membranoproliferative Glomerulonephritis Type II: Dense Deposit Disease, DDD
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Kwon HS, Oh SJ, Lee YM, Kim JH, Kim PK, Kang HY, Jeong HJ, Choi IJ
- KMID: 2144705
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):188-195.
Type II membranoproliferative glomerulonephritis (Dense deposit disease ) is an acquired primary glomerular disease characterized by electron microscopic evidence of a continuous dense membrane deposition replacing the lamina densa. It... -
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- Increased Frequency of Apolipoprotein E4 Genotype in Childhood Minimal Change Nephrotic Syndrome (MCNS)
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Kim SD, Bae YM, Cho BS, Cho YW, Kim IS
- KMID: 2144694
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):87-99.
PURPOSE: We studied to find out apo-E genotype polymorphism in minimal change nephrotic syndrome(MCNS) and IgA nephropathy(IgAN) and to determine the relationship between apo-E genotype and clinical course of MCNS. MATERIALS... -
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- A Case of Microscopic Polyangiitis with Pulmonary Hemorrhage and Rapidly Progressive Glomerulonephritis
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Kwon HS, Lee YM, Kim JH, Kim PK, Kang HY, Hong SW, Jeong HJ
- KMID: 2144709
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):213-218.
Microscopic Polyangiitis(MPA) belongs to a spectrum of systemic vasculits, and particularly antineutrophil cytoplasmic autoantibodies(ANCA)-associated small-vessel vasculitis which is characterized by involvement of the lung and kidney. The diagnosis of MPA... -
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- Pulmonary Embolism In Childhood Minimal Change Nephrotic Syndrome
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Sung SJ, Hong KW, Kim ER, Kim IS, Cho BS
- KMID: 2144695
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):100-108.
PURPOSE:We investigated the incidence and predisposing factors of pulmonary embolism in minimal change nephrotic syndrome(MCNS). METHODS:Lung perfusion scan using 99mTC-MAA were done on 14 patients who were diagnosed... -
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- The Effect of Levamisole in Steroid-Dependent Nephrotic Syndrome in Children
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Han JH, Lee KJ, Lee YM, Kim JH, Kim PK
- KMID: 2144696
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):109-116.
PURPOSE: Long-term use of steroid, cyclophosphamide and cyclosporin, which are frequently used in the therapy of SDNS, might cause severe side effects. Recently, the immune-modulator levamisole has been tried as... -
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- The Effects of Intravenous Methylprednisolone Pulse Therapy by Mendoza Protocol in Primary and Secondary Nephrotic Syndrome
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Lee KJ, Han JH, Lee YM, Kim JH, Kim PK
- KMID: 2144697
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):117-124.
PURPOSE: Since Mendoza(1990)'s report that long term methylprednisolone pulse therapy by Mendoza protocol (MP therapy) is a good treatment option in focal segmental glomerulo -sclerosis(FSGS), there have been reports of... -
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- Analysis of Urinary Mass Screening for Second Grade of Elemantary School Children in Paju City
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Kim SK, Kim YK, Park YW, Lee CG
- KMID: 2144701
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):156-163.
PURPOSE: We performed urinary mass screening(UMS) program for 2,804 children of second grade elemantary school 8 years of age in Paju city with cooperation of Paju City Health Center to... -
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- The Significance of Hyperlipidemia as a Predictive Factor of Relapse in Corticosensitive Nephrotic Syndrome
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Jung SP, Hong SC, Lim SJ, Lim IS, Choi ES
- KMID: 2144699
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):136-146.
PURPOSE: One of the most difficult problems in the care of children with nephrotic syndrome remains the occurrence of relapses, despite initial response to steroids. Constantinescu reported that rapidity of... -
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- Risk Factors Affecting Long-term Outcome of Alport syndrome
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Byun JY, Baek SY, Lee YM, Kim JH, Lee JS, Kim PK, Hong SW, Jeong HJ, Kim SI, Kim YS, Park KI
- KMID: 2144702
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):164-175.
PURPOSE: Alport syndrome is a hereditary nephrotic disease characterized by progressive nephrotic symptom, sensorineural hearing loss, ophthalmic abnormality, typical microscopic findings, and familial occurrence. In this study, we tried to... -
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- Analysis of Childhood Rapidly Progressive Glomerulonephritis
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Uhm JH, Kim MJ, Lee YM, Kim JH, Lee JS, Kim PK, Hong SW, Jeung HJ
- KMID: 2144693
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):78-86.
PURPOSE:Rapidly progressive glomerulonephritis (RPGN) is characterized by the rapid increase in serum creatitnin and crescents formation involving more than 50% of glomeruli. 10 patients who had been treated for RPGN... -
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- A Comparative Analysis of the Clinical and Pathological Features of IgA Nephropathy and Thin Glomerular Basement Membrane Disease
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Chi GH, Ha CW, Kim YJ, Yoon HK, Chung WY
- KMID: 2144700
- J Korean Soc Pediatr Nephrol.
- 2001 Oct;5(2):147-155.
PURPOSE: IgA nephropathy(IgAN) and thin glomerular basement membrane disease(TGBMD) are common glomerular diseases that cause hematuria in childhood. IgAN has characteristics of IgA deposit as the sole or predominantly localized... -
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