- CRISPR-Cas9 system in autosomal dominant polycystic kidney disease: a comprehensive review
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Kang S, Park SJ, Lee MH, Kronbichler A, Shin JI
- KMID: 2565475
- Child Kidney Dis.
- 2025 Feb;29(1):4-11.
- doi: 10.3339/ckd.25.008
Genetic kidney diseases are caused by mutations in specific genes that significantly affect kidney development and function. Although the underlying pathogenic genes of many kidney diseases have been identified, an... -
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- Biomarkers for the early diagnosis of Alport syndrome and associated kidney damage
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Nguyen HDT, Cho MH
- KMID: 2565476
- Child Kidney Dis.
- 2025 Feb;29(1):12-18.
- doi: 10.3339/ckd.25.004
Alport syndrome (AS) is a hereditary nephropathy characterized by progressive kidney damage that commonly leads to endstage kidney disease. Early diagnosis is critical, as preemptive nephroprotective therapy, such as angiotensin-converting... -
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- How to treat recurrent focal segmental glomerulosclerosis after kidney transplantation in children
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Park PG
- KMID: 2565477
- Child Kidney Dis.
- 2025 Feb;29(1):19-23.
- doi: 10.3339/ckd.25.002
Focal segmental glomerulosclerosis (FSGS), a significant cause of kidney failure in children, is a common pathological diagnosis in cases of idiopathic nephrotic syndrome, especially steroid-resistant ones. FSGS has the potential... -
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- Acute kidney injury in very low birth weight infants: challenges, risk factors, and outcomes
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Kim JY
- KMID: 2565474
- Child Kidney Dis.
- 2025 Feb;29(1):1-3.
- doi: 10.3339/ckd.25.006
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- Clinicopathological differences in the activation pattern of the complement system between pediatric and adult lupus nephritis: a single centered retrospective study in Korea
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Park MJ, Han MH, Kim Ms, Kim YJ, Lee SJ, Kim D, Baek HS, Cho MH
- KMID: 2565478
- Child Kidney Dis.
- 2025 Feb;29(1):24-31.
- doi: 10.3339/ckd.25.001
Purpose: Lupus nephritis (LN) can be caused by the complement activation. This study aimed to investigate the differences and clinical implications of the activation pattern of the complement system for... -
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- Incidentally detected bilateral sub-internal limiting membrane hemorrhages in typical hemolytic uremic syndrome: a case report
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Kwon HJ, Song JY
- KMID: 2565479
- Child Kidney Dis.
- 2025 Feb;29(1):32-38.
- doi: 10.3339/ckd.25.003
We present an incidentally detected case of bilateral sub-internal limiting membrane (ILM) hemorrhage secondary to typical hemolytic uremic syndrome (HUS) along with a literature review. A 4-year-old girl presented to... -
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