- Pediatric Hemodialysis
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Cho H
- KMID: 2508543
- Child Kidney Dis.
- 2020 Oct;24(2):69-74.
- doi: 10.3339/jkspn.2020.24.2.69
Hemodialysis is rarely used in neonates and infants due to the risk of major complications in the very young. Nevertheless, there are clinical situations where hemodialysis is needed and may... -
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- Infectious and Non-infectious Complications of Peritoneal Dialysis in Children
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Cho MH
- KMID: 2508542
- Child Kidney Dis.
- 2020 Oct;24(2):63-68.
- doi: 10.3339/jkspn.2020.24.2.63
Despite the many advantages of peritoneal dialysis (PD) in children with endstage renal disease, there exist redoubtable complications of PD that should be overcome. To prevent and manage these complications,... -
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- Malignancy after Pediatric Kidney Transplantation: The 30-Year Experience of a Single Center
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Jung J, Park YS, Han DJ
- KMID: 2508544
- Child Kidney Dis.
- 2020 Oct;24(2):75-82.
- doi: 10.3339/jkspn.2020.24.2.75
Objectives: We aimed to investigate the incidence, manifestations, and outcomes of malignancy after pediatric kidney transplantation (KT) at our center over 30 years. Methods: We retrospectively reviewed the medical records of... -
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- A Pediatric Case of AVPR2-related Nephrogenic Syndrome of Inappropriate Antidiuresis
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Bae H, Baek HS, Jang HM, Lee EJ, Cho MH
- KMID: 2508551
- Child Kidney Dis.
- 2020 Oct;24(2):126-130.
- doi: 10.3339/jkspn.2020.24.2.126
Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is a rare X-linked genetic condition caused by a gain-of-function mutation of arginine vasopressin receptor 2 gene, AVPR2. We report the case of a... -
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- Rapid Resolution of Atypical Hemolytic Uremic Syndrome by Eculizumab Treatment
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Kim MS, Lim SH, Kim JH, Ha IS, Cheong HI, Kang HG
- KMID: 2508553
- Child Kidney Dis.
- 2020 Oct;24(2):138-142.
- doi: 10.3339/jkspn.2020.24.2.138
Atypical hemolytic uremic syndrome (aHUS) is an extremely rare and life-threatening disorder. Typical HUS is often caused by Shiga toxin-positive Escherichia coli, while aHUS is caused by dysregulation of the... -
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- 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: 2508548
- Child Kidney Dis.
- 2020 Oct;24(2):107-114.
- doi: 10.3339/jkspn.2020.24.2.107
Purpose: The purpose of this study was to evaluate the prevalence, clinical characteristics, and long-term clinical effects of hypertension in Korean childhood-onset systemic lupus erythematous (SLE) patients. Methods: The medical records... -
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- Gorham-Stout Syndrome with Focal Segmental Glomerulosclerosis: A Case Report
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Kim JH, Kim YS, Lim SH, Ahn YH, Ko JM, Suh DI, Lee KB, Moon KC, Ha IS, Cheong HI, Kang HG
- KMID: 2508550
- Child Kidney Dis.
- 2020 Oct;24(2):120-125.
- doi: 10.3339/jkspn.2020.24.2.120
Gorham-Stout syndrome is a rare bone disorder characterized by progressive massive osteolysis and proliferation of vascular and lymphatic vessels. A 15-year-old boy was initially diagnosed with Gorham-Stout at the age... -
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- A Case of Nephrogenic Diabetes Insipidus with a Rare X-linked Recessive Mutation in an Infant with Developmental and Growth Retardation Tracked by the Korean National Health Screening Program
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Kim MJ, Cho JY, Park JS, Park ES, Seo JH, Lim JY, Woo HO, Youn HS
- KMID: 2508552
- Child Kidney Dis.
- 2020 Oct;24(2):131-137.
- doi: 10.3339/jkspn.2020.24.2.131
Nephrogenic diabetes insipidus (DI) is a rare disease in which the patient cannot concentrate urine despite appropriate or high secretion of antidiuretic hormone. Congenital nephrogenic DI is caused by the... -
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- Association of Neutrophil Gelatinase associated Lipocalin and Leukocyte Differential Count in Children with Febrile Urinary Tract Infections
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Jang JW, Yim HE, Yoo KH
- KMID: 2508545
- Child Kidney Dis.
- 2020 Oct;24(2):83-90.
- doi: 10.3339/jkspn.2020.24.2.83
Purpose: To investigate the association between urinary neutrophil gelatinaseassociated lipocalin (uNGAL) and leukocyte differential count in children with urinary tract infections (UTIs). Methods: A retrospective chart review was performed in children... -
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- Vesicoureteral Reflux and Renal Scarring in Children with Acute Pyelonephritis: the Role of Late 6-month Dimercaptosuccinic Acid Renal Scan
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Oh KE, Yim HE, Yoo KH
- KMID: 2508547
- Child Kidney Dis.
- 2020 Oct;24(2):98-106.
- doi: 10.3339/jkspn.2020.24.2.98
Purpose: The aim of this study is to evaluate the clinical utility of late 6-month dimercapto-succinic acid (DMSA) renal scan in predicting vesicoureteral reflux (VUR) and long-lasting renal scars in... -
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- Clinical Characteristics and Long-Term Prognosis of Alport Syndrome: A Retrospective Single-Center Study
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Jang HM, Baek HS, Park SH, Kim YL, Kim CD, Jung HY, Cho JH, Han MH, Kim YJ, Cho MH
- KMID: 2508546
- Child Kidney Dis.
- 2020 Oct;24(2):91-97.
- doi: 10.3339/jkspn.2020.24.2.91
Purpose: Alport syndrome (AS) is one of the most common inherited renal diseases caused due to mutations of genes encoding specific proteins of the type IV collagen family, and its... -
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- A Pediatric Case of Long-term Untreated Distal Renal Tubular Acidosis
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Kedsatha P, Shin HY, Choi Y, Cheong HI, Cho TJ, Yi E, Maisai M
- KMID: 2508549
- Child Kidney Dis.
- 2020 Oct;24(2):115-119.
- doi: 10.3339/jkspn.2020.24.2.115
Distal renal tubular acidosis (dRTA) is a rare renal tubular disorder characterized by normal anion gap metabolic acidosis, hypokalemia, and high urine pH. It can be inherited or acquired. In... -
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