- Effect of Hypertension on Childhood-onset Systemic Lupus Erythematous in a Tertiary Medical Center in Korea
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Kim JY, Cho H
- KMID: 2518370
- Child Kidney Dis.
- 2021 Jun;25(1):49-49.
- doi: 10.3339/jkspn.2021.25.1.49
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- Pediatric Kidney Transplantation
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Lee YH, Kang HG
- KMID: 2518363
- Child Kidney Dis.
- 2021 Jun;25(1):8-13.
- doi: 10.3339/jkspn.2021.25.1.8
Pediatric kidney transplantation is the best option since it can achieve near normal glomerular filtration rate, adequate fluid balance, and autonomic endocrine function of the kidney in end-stage kidney disease.... -
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- Risk Factors for the Progression of Chronic Kidney Disease in Children
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Ahn YH, Kang HG, Ha IS
- KMID: 2518362
- Child Kidney Dis.
- 2021 Jun;25(1):1-7.
- doi: 10.3339/jkspn.2021.25.1.1
Chronic kidney disease (CKD) in children is associated with various complications, including poor growth and development, mineral bone disorder, cardiovascular disease, kidney failure, and mortality. Slowing down the progression of... -
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- Clinical Genetic Testing in Children with Kidney Disease
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Kang E, Lee BH
- KMID: 2518364
- Child Kidney Dis.
- 2021 Jun;25(1):14-21.
- doi: 10.3339/jkspn.2021.25.1.14
Chronic kidney disease, the presence of structural and functional abnormalities in the kidneys, is associated with a lower quality of life and increased morbidity and mortality in children. Genetic etiologies... -
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- A Case of Idiopathic Renal Hypouricemia with SLC22A12 Gene Mutation Showing General Weakness and Incidental Renal Stone
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Joung JW, Song YW, Kim JD, Cheon EJ
- KMID: 2518369
- Child Kidney Dis.
- 2021 Jun;25(1):44-48.
- doi: 10.3339/jkspn.2021.25.1.44
Idiopathic renal hypouricemia (iRHUC) is a rare hereditary disease caused by a defect in urate handling of renal tubules. Type 1 renal hypouricemia (RHUC1) is diagnosed with confirmation of a... -
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- Enuresis as a Presenting Symptom of Graves’ Disease: A Case Report
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Hwang I, Park E, Lee HJ
- KMID: 2518368
- Child Kidney Dis.
- 2021 Jun;25(1):40-43.
- doi: 10.3339/jkspn.2021.25.1.40
Enuresis is intermittent urinary incontinence during sleep at night in children aged 5 years or older. The main pathophysiology of enuresis involves nocturnal polyuria, abnormal sleep arousal, and low functional... -
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- A Novel Homozygous CLCNKB Mutation of Classic Bartter Syndrome Presenting with Renal Cysts in 6-year-Old Identical Twin Boys : A Case Report
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Son MH, Yim HE, Yoo KH
- KMID: 2518367
- Child Kidney Dis.
- 2021 Jun;25(1):35-39.
- doi: 10.3339/jkspn.2021.25.1.35
Bartter syndrome is an autosomal recessive hypokalemic salt-losing tubulopathy, and classic Bartter syndrome is associated with mutations in the CLCNKB gene. While chronic hypokalemia is known to induce renal cyst... -
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- Clinical Outcomes of Non-carbapenem Treatment for Urinary Tract Infections Caused by Extended-spectrum β-lactamase-producing Escherichia coli
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Kim E, Ahn YH, Lee JW, Park E
- KMID: 2518365
- Child Kidney Dis.
- 2021 Jun;25(1):22-28.
- doi: 10.3339/jkspn.2021.25.1.22
Purpose: The purpose of this study was to investigate the clinical outcomes of non-carbapenem treatment for urinary tract infections (UTIs) caused by extended-spectrum β-lactamase (ESBL)-producing Escherichia coli (E. coli) in... -
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- C3 Glomerulonephritis associated with Anti-complement Factor H Autoantibodies in an Adolescent Male: A Case Report
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Hyun H, Kang HG, Cho U, Ha IS, Cheong HI
- KMID: 2518366
- Child Kidney Dis.
- 2021 Jun;25(1):29-34.
- doi: 10.3339/jkspn.2021.25.1.29
C3 glomerulonephritis (C3GN), a rare condition associated with dysregulation of the alternative pathway of the complement system, is histopathologically characterized by isolated or dominant C3 deposition in the renal glomeruli.... -
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