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A Case of Nutcracker Syndrome Presenting with Orthostatic Proteinuria

Kim YB, Baek SC, Yoo HJ, Kim CH, Lee HH, Kim PK, Park NH

  • KMID: 2197659
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):74-79.
Orthostatic proteinuria is documented as a benign condition and the most common cause of isolated proteinuria. The etiology and pathogenesis of orthostatic proteinuria is not clear yet. Recently there were...
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Hypertensive Encephalopathy in a 10-year-old Boy with Ureteral Stone

Kim YJ, Kang HC, Koo JW

  • KMID: 2197653
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):51-56.
Hypertensive encephalopathy is an acute neurologic syndrome that occurs in association with abrupt and marked elevation of blood pressure and is characterized by headache, vomiting, seizure, visual disturbances and altered...
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A Case of Steroid-responsive Pericardial Effusion as an Initial Manifestation of Childhood Systemic Lupus Erythematosus

Lee JS, Ha TS

  • KMID: 2197661
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):80-85.
The systemic lupus erythematosus(SLE) is a systemic inflammatory disease caused by autoimmune mechanism, involving blood cells, the kidney, the central nervous system, and etc. The heart is one of the...
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A Case of Transient Pseudohypoaldosteronism Secondary to Ureteropelvic Junction Obstruction

Choi J, Hahn H, Park YS, You HW

  • KMID: 2197669
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):91-95.
We report a 2-month-old boy who presented with severe hyponatremia and hyperkalemia secondary to ureteropelvic junction(UPJ) obstruction. By prenatal ultrasonography at 19 weeks of gestation, severe hydronephrosis was found which...
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Distal Renal Tubular Acidosis Complicated with Periodic Hypokalemic Paralysis

Park JM, Noh BH, Shin JI, Kim MJ, Lee JS

  • KMID: 2197655
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):63-67.
A 5-year-old girl was admitted because of an acute onset of weakness in her extremities. She had experienced a similar episode before but had recovered spontaneously. She had previously been...
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A Case of Hemolytic Uremic Syndrome in a Child with Ischemic Colitis

Kim YH, Ahn SY, Park JM, Lee JS

  • KMID: 2197665
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):86-90.
Hemolytic uremic syndrome(HUS) is characterized by acute renal failure, microangiopathic hemolytic anemia, and thrombocytopenia and the most common pathogen is Escherichia coli (E. coli) O157:H7. Ischemic colitis, which rarely occurs...
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A Case of Schinzel-Giedion Syndrome

Jeoung MJ, Yim HE, Yoo KH, Hong YS, Lee JW, Kim SK

  • KMID: 2197654
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):57-62.
Schinzel-Giedion syndrome is a rare, distinct dysmorphic syndrome characterized by congenital hydronephrosis, skeletal dysplasia, and severe developmental retardation, likely to be inherited as an autosomal recessive trait, but not yet...
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A Case of Gitelman Syndrome Presented with Epileptic Seizure

Park JM, Kim JT, Shin JI, Kim HD, Kim TY, Cheong HI, Lee JS

  • KMID: 2197657
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):68-73.
Both Gitelman syndrome and Bartter syndrome are autosomal recessively inherited renal tubular disorders characterized by hypokalemic metabolic alkalosis, salt wasting and normal to low blood pressure. Gitelman syndrome is caused...
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Effect of Tumor Necrosis Factor-Alpha on Glomerular Epithelial Cells in Glomerular Permeability

Cho MH, Lee JH, Ko CW, Koo JH

  • KMID: 2197647
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):1-9.
PURPOSE: Minimal Change Disease (MCD) is the most common primary nephrotic syndrome in children. Some suggested that tumor necrosis factor-alpha (TNF-alpha) are involved in the pathogenesis of MCD. METHODS: This study...
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Angiotensinogen M235T Polymorphism in Children with Henoch-Schonlein Purpura Nephritis

Ha CW, Joo HJ, Park JK, Chung WY

  • KMID: 2197648
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):10-17.
PURPOSE: Henoch-Schonlein purpura(HSP) nephritis has a variable range of prevalence from 25 to 50% among HSP patients and is a common cause of chronic glomerulonephritis in children. In our study,...
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Plasminogen Activator Inhibitor Type 1 Gene Polymorphism in Patients with Minimal Change Nephrotic Syndrome

Kim YM, Hong HK, Kim SD, Cho BS

  • KMID: 2197650
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):26-32.
PURPOSE: Hypercoagulability is present in patients with nephrotic syndrome. Plasminogen activator inhibitor type 1(PAI-1) is a major inhibitor of plasminogen activators. PAI-1 inactivates both tissue plasminogen activator(tPA) and urokinase plasminogen...
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Efficacy of Pamidronate in Nephropathic Children with Ongoing Long Term Corticosteroid Therapy

Hong HK, Kim ES, Kim SD, Cho BS

  • KMID: 2197652
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):43-50.
BACKGROUND: Steroid-induced osteoporosis(SIO) is one of the serious complications of long- term steroid therapy, especially in growing children. Recently bisphosphonates have been used to treat or prevent SIO in adult,...
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Angiotensin Converting Enzyme Gene Polymorphism in Alport Syndrome

Kim JH, Lee JS, Kim PK

  • KMID: 2197649
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):18-25.
PURPOSE: Alport syndrome is clinically characterized by hereditary progressive nephritis causing ESRD with irregular thickening of the GBM and sensory neural hearing loss. The mutations of type IV collagen gene(COL4A5)...
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Therapeutic Efficacy of Alendronate for Glucocorticoid Induced Metabolic Bone Disease in Children with Nephrotic Syndrome

Lee JE, Lee HO, Paik KH, Lee SH, Jin DK

  • KMID: 2197651
  • J Korean Soc Pediatr Nephrol.
  • 2004 Apr;8(1):33-42.
PURPOSE: Children with nephrotic syndrome(NS) are under high risk for metabolic bone disease(MBD) as a complication of long-term glucocorticoid therapy. We prospectively evaluated the effect of oral bisphosphonate(alendronate) therapy in...
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