- CUBN mutation, a genetic cause of persistent proteinuria in children
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Suh JS
- KMID: 2560475
- Child Kidney Dis.
- 2024 Oct;28(3):87-89.
- doi: 10.3339/ckd.24.019
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- Nutcracker syndrome in pediatrics: a rare entity?
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Yim HE
- KMID: 2560476
- Child Kidney Dis.
- 2024 Oct;28(3):90-92.
- doi: 10.3339/ckd.24.014
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- Association between serum uric acid and kidney disease with pediatric focus
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Cho MH
- KMID: 2560479
- Child Kidney Dis.
- 2024 Oct;28(3):106-111.
- doi: 10.3339/ckd.24.016
Hyperuricemia is a global medical issue. Kidney disease and hyperuricemia are clearly related. Whether uric acid is a disease bystander or a therapeutic target in chronic kidney disease (CKD) remains... -
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- Congenital solitary functioning kidney: evaluations to do which, when, and how
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Lee HK
- KMID: 2560478
- Child Kidney Dis.
- 2024 Oct;28(3):99-105.
- doi: 10.3339/ckd.24.013
Congenital solitary functioning kidney (CSFK) is characterized by an anatomical or functional absence of one kidney from birth. When suspected on perinatal ultrasonography (US), repeat US after birth should be... -
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- Diet as a treatment for chronic kidney disease
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Jung J, Lee JH
- KMID: 2560480
- Child Kidney Dis.
- 2024 Oct;28(3):112-115.
- doi: 10.3339/ckd.24.017
The management of chronic kidney disease (CKD) includes nutritional interventions aimed at slowing disease progression and mitigating complications. This review examines various dietary approaches for CKD treatment, focusing on carbohydrate... -
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- C3 glomerulonephritis with genetically confirmed C3 deficiency in a pediatric patient: a case report
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Kim HM, Shin JI, Kim JH, Oh J, Kang JM, Kang HG, Kim SH, Cho BS, Lee KH
- KMID: 2560482
- Child Kidney Dis.
- 2024 Oct;28(3):124-130.
- doi: 10.3339/ckd.24.015
Complement component 3 glomerulonephritis (C3GN) is a rare kidney disease characterized by complement dysregulation that results in prominent complement component 3 (C3) deposition in the kidneys. The clinical course of... -
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- Integrating predictive modeling and causal inference for advancing medical science
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Oh TR
- KMID: 2560477
- Child Kidney Dis.
- 2024 Oct;28(3):93-98.
- doi: 10.3339/ckd.24.018
Artificial intelligence (AI) is revolutionizing healthcare by providing tools for disease prediction, diagnosis, and patient management. This review focuses on two key AI methodologies in healthcare: predictive modeling and causal... -
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- Assessing the prognostic impact of KDIGO criteria on acute kidney injury in very low birth weight infants: a critical insight
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Pasini LF, Kuchart LdL, Bilibio SA, Santa Catarina RF, Araújo BFd, Selistre LdS, de Souza VC
- KMID: 2560481
- Child Kidney Dis.
- 2024 Oct;28(3):116-123.
- doi: 10.3339/ckd.24.012
Purpose: To evaluate the incidence and identify risk factors for acute kidney injury (AKI) within the first 15 days of life in very low birth weight (VLBW) infants in a... -
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- Lupus anticoagulant-hypoprothrombinemia syndrome with lupus nephritis in a girl misdiagnosed with immunoglobulin A nephropathy: a case report
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Lee CH, Ahn YH, Kang HG, Kim JH
- KMID: 2560483
- Child Kidney Dis.
- 2024 Oct;28(3):131-137.
- doi: 10.3339/ckd.24.021
Distinguishing lupus nephritis (LN) from other glomerulopathies, such as immunoglobulin A nephropathy (IgAN), poses a diagnostic challenge owing to overlapping clinical and histopathologic findings. Lupus anticoagulant-hypoprothrombinemia syndrome (LAHPS) is a... -
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