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


Nutcracker syndrome in pediatrics: a rare entity?
Hyung Eun Yim
Child Kidney Dis. 2024;28(3):90-92.

Special Article

October 31, 2024


Integrating predictive modeling and causal inference for advancing medical science
Tae Ryom Oh
Child Kidney Dis. 2024;28(3):93-98.

Review Article

October 2, 2024


Congenital solitary functioning kidney: evaluations to do which, when, and how
Hyun Kyung Lee
Child Kidney Dis. 2024;28(3):99-105.

Review Article

October 22, 2024


Association between serum uric acid and kidney disease with pediatric focus
Myung Hyun Cho
Child Kidney Dis. 2024;28(3):106-111.

Review Article

October 31, 2024


Diet as a treatment for chronic kidney disease
Jiwon Jung, Joo Hoon Lee
Child Kidney Dis. 2024;28(3):112-115.

Original Article

September 27, 2024


Assessing the prognostic impact of KDIGO criteria on acute kidney injury in very low birth weight infants: a critical insight
Laís Fagundes Pasini, Léia de Lima Kuchart, Sarah Assoni Bilibio, et al.
Child Kidney Dis. 2024;28(3):116-123.

Case Report

October 31, 2024


C3 glomerulonephritis with genetically confirmed C3 deficiency in a pediatric patient: a case report
Hae Min Kim, Jae Il Shin, Ji Hong Kim, et al.
Child Kidney Dis. 2024;28(3):124-130.

Case Report

October 31, 2024


Lupus anticoagulant-hypoprothrombinemia syndrome with lupus nephritis in a girl misdiagnosed with immunoglobulin A nephropathy: a case report
Chung Ho Lee, Yo Han Ahn, Hee Gyung Kang, et al.
Child Kidney Dis. 2024;28(3):131-137.

Most-cited are based on citations from 2023 ~ 2025.

Review Article
808
Management of hydronephrosis: a comprehensive review in pediatric urology perspective
Sang Woon Kim
Child Kidney Dis. 2024;28(2):59-65.   Published online June 28, 2024
View: 2748   Download: 81  Citations: 2
Original Article
806
Effect of renal Doppler ultrasound on the detection of nutcracker syndrome in children presenting orthostatic proteinuria
Eun Jae Hwang, Ji Hong Kim, Mi-Jung Lee, Haesung Yoon, Jae Il Shin, Keum Hwa Lee
Child Kidney Dis. 2024;28(2):74-79.   Published online June 28, 2024
View: 2073   Download: 90  Citation: 1
Review Article
800
Navigating the landscape of clinical genetic testing: insights and challenges in rare disease diagnostics
Soo Yeon Kim
Child Kidney Dis. 2024;28(1):8-15.   Published online February 28, 2024
View: 3358   Download: 35  Citation: 1
802
Advances in the use of dried blood spots on filter paper to monitor kidney disease
Carla Nicola, Vandréa de Souza
Child Kidney Dis. 2024;28(1):16-26.   Published online February 28, 2024
View: 3884   Download: 75  Citation: 1
793
Tolvaptan: a possible preemptive treatment option in children with autosomal dominant polycystic kidney disease?
Hee Sun Beak, Min Hyun Cho
Child Kidney Dis. 2023;27(2):76-81.   Published online December 26, 2023
View: 1862   Download: 36  Citation: 1
795
Anemia in children with chronic kidney disease
Min Ji Park, Min Hyun Cho
Child Kidney Dis. 2023;27(2):82-88.   Published online December 26, 2023
View: 2757   Download: 94  Citation: 1
796
Nutcracker syndrome in children: review of symptom, diagnosis, and treatment
Diana S. Kalantar, Se Jin Park, Jae Il Shin
Child Kidney Dis. 2023;27(2):89-96.   Published online December 29, 2023
View: 3789   Download: 58  Citation: 1
780
CUBN mutation: a benign genetic cause of proteinuria?
Hyun Kyung Lee
Child Kidney Dis. 2023;27(1):19-25.   Published online June 14, 2023
View: 2279   Download: 79  Citation: 1

Childhood
Kidney Diseases

Print ISSN: 2384-0242
Online ISSN: 2384-0250

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