- Cell-derived Secretome for the Treatment of Renal Disease
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Kim MW, Ko IK, Atala A, Yoo JJ
- KMID: 2464930
- Child Kidney Dis.
- 2019 Oct;23(2):67-76.
- doi: 10.3339/jkspn.2019.23.2.67
Kidney disease is a major global health issue. Hemodialysis and kidney transplantation have been used in the clinic to treat renal failure. However, the dialysis is not an effective long-term... -
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- Genetic Basis of Steroid Resistant Nephrotic Syndrome
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Park E
- KMID: 2464932
- Child Kidney Dis.
- 2019 Oct;23(2):86-92.
- doi: 10.3339/jkspn.2019.23.2.86
Steroid-resistant nephrotic syndrome (SRNS) has long been a challenge for clinicians due to its poor responsiveness to immunosuppressants, and rapid progression to end-stage renal disease. Identifying a monogenic cause for... -
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- Pathology of C3 Glomerulopathy
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Shin SJ, Seong Y, Lim BJ
- KMID: 2464933
- Child Kidney Dis.
- 2019 Oct;23(2):93-99.
- doi: 10.3339/jkspn.2019.23.2.93
C3 glomerulopathy is a renal disorder involving dysregulation of alternative pathway complement activation. In most instances, a membranoproliferative pattern of glomerular injury with a prevalence of C3 deposition is observed... -
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- Contrast-Associated Acute Kidney Injury (CA-AKI) in Children: Special Considerations
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Windpessl , Kronbichler A
- KMID: 2464931
- Child Kidney Dis.
- 2019 Oct;23(2):77-85.
- doi: 10.3339/jkspn.2019.23.2.77
Contrast-associated acute kidney injury (CA-AKI) is a major concern when iodinated contrast material is administered, especially in patients at risk. Efforts have been undertaken to understand the detrimental effects of... -
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- Bilateral Ureteral Obstruction Related to Pelvic Rhabdomyosarcoma Presenting with Acute Kidney Injury: A Case Report
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Han S, Han KH
- KMID: 2464937
- Child Kidney Dis.
- 2019 Oct;23(2):116-120.
- doi: 10.3339/jkspn.2019.23.2.116
Bilateral renal obstruction is a rare critical condition, requiring a prompt diagnostic approach and treatment to restore the renal function. The most commonly observed obstructive uropathy in children is congenital... -
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- A Case of Henoch-Schönlein Purpura with Fulminant Complications and Its Long-term Outcome
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Lee DH, LEE ES, Hong J, Park KH, Pai KS
- KMID: 2464940
- Child Kidney Dis.
- 2019 Oct;23(2):128-133.
- doi: 10.3339/jkspn.2019.23.2.128
Henoch-Schönlein purpura (HSP) is a systemic vasculitis characterized by purpura, arthritis, abdominal pain, and nephritis. Gastrointestinal involvement can manifest as pain, intussusception, intestinal bleeding, and intestinal perforation. We report a... -
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- A Case of Infantile Fungal Urinary Tract Infection
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Cho W, Jo YM, Oh YK, Rim JW, Lee WU, Choi K, Ko JH, Jeon YJ, Choi Y
- KMID: 2464938
- Child Kidney Dis.
- 2019 Oct;23(2):121-123.
- doi: 10.3339/jkspn.2019.23.2.121
Urinary tract infection is common in the pediatric population. The most common causative agents are bacteria, among which Escherichia coli is the most frequent uropathogen. Although fungal urinary tract infection... -
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- Herlyn-Werner-Wunderlich Syndrome with Central Precocious Puberty: A Case Report
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Han J, Lee JM, Kim GH, Kim SJ
- KMID: 2464939
- Child Kidney Dis.
- 2019 Oct;23(2):124-127.
- doi: 10.3339/jkspn.2019.23.2.124
Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly of the genitourinary tract comprising uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. Patients with HWW syndrome usually present symptoms such as... -
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- Primary Hyperoxaluria in Korean Pediatric Patients
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Choe Y, Lee JM, Kim JH, Cho MH, Kim SH, Lee JH, Park YS, Kang HG, Ha IS, Cheong HI
- KMID: 2464929
- Child Kidney Dis.
- 2019 Oct;23(2):59-66.
- doi: 10.3339/jkspn.2019.23.2.59
BACKGROUND: Primary hyperoxaluria (PH), a rare inborn error of glyoxylate meta bolism causing overproduction of oxalate, is classified into three genetic subgroups: type 1–3 (PH1–PH3) caused by AGXT, GRHPR ,... -
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- The associations of Urinary Neutrophil Gelatinaseassociated Lipocalin (NGAL) and Liver-type Fatty Acidbinding Protein (L-FABP) Levels with Hematuria in Children and Adolescents
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Choi Y, Bin JH, Cho KS, Lee J, Suh JS
- KMID: 2464935
- Child Kidney Dis.
- 2019 Oct;23(2):105-110.
- doi: 10.3339/jkspn.2019.23.2.105
PURPOSE: We sought to determine associations of urinary neutrophil gelatinase-associated lipocalin (NGAL) and liver-type fatty acid-binding protein (L-FABP), known markers of renal injury, with hematuria in children and adolescents. METHODS: A... -
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- Clinical Characteristics of Ureteral Duplication in Children
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Park MJ, Baek HS, Jang HM, Lee JN, Chung SK, Jeong SY, Lee SM, Cho MH
- KMID: 2464934
- Child Kidney Dis.
- 2019 Oct;23(2):100-104.
- doi: 10.3339/jkspn.2019.23.2.100
PURPOSE: Ureteral duplication is a relatively common congenital urinary tract abnormality that can be associated with various clinical problems such as vesicoureteral reflux (VUR), hydronephrosis, and ectopic ureters. The purpose... -
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- Vitamin D Dependent Rickets Type 1A Caused by CYP27B1 Mutation
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Bak NR, Song ES, Yang EM, Kim CJ
- KMID: 2464936
- Child Kidney Dis.
- 2019 Oct;23(2):111-115.
- doi: 10.3339/jkspn.2019.23.2.111
Vitamin D dependent rickets type 1A (VDDR1A) is an autosomal recessive disorder caused by mutations in CYP27B1 . Clinical findings are growth retardation, hypotonia, muscle weakness, hypocalcemic seizures, and radiological... -
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