-
Editorial
October 22, 2024
- CUBN mutation, a genetic cause of persistent proteinuria in children
- Jin-Soon Suh
- Child Kidney Dis. 2024;28(3):87-89.
Editorial
October 22, 2024
Editorial
October 22, 2024
Special Article
October 31, 2024
Review Article
October 2, 2024
Review Article
October 22, 2024
Review Article
October 31, 2024
Original Article
September 27, 2024
Case Report
October 31, 2024
Case Report
October 31, 2024
This archive contains links to the full-text of all issues of Child Kidney Dis.
Childhood
Kidney Diseases
Print ISSN: 2384-0242
Online ISSN: 2384-0250
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Mechanism, clinical consequences, and management of dyslipidemia in children with nephrotic syndrome |
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Hematuria in children: causes and evaluation |
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Management strategies for congenital isolated hydronephrosis and the natural course of the disease |
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Impact of COVID-19 on the clinical course of nephrotic syndrome in children: a single-center study |
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Infectious inflammation in children with acute pyelonephritis |
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Mechanism, clinical consequences, and management of dyslipidemia in children with nephrotic syndrome |
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Alport syndrome: new advances in the last decade |