Skip Navigation
Skip to contents
Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

6 results
Display

CRISPR-Cas9 system in autosomal dominant polycystic kidney disease: a comprehensive review

Kang S, Park SJ, Lee MH, Kronbichler A, Shin JI

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Biomarkers for the early diagnosis of Alport syndrome and associated kidney damage

Nguyen HDT, Cho MH

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
How to treat recurrent focal segmental glomerulosclerosis after kidney transplantation in children

Park PG

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acute kidney injury in very low birth weight infants: challenges, risk factors, and outcomes

Kim JY

CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinicopathological differences in the activation pattern of the complement system between pediatric and adult lupus nephritis: a single centered retrospective study in Korea

Park MJ, Han MH, Kim Ms, Kim YJ, Lee SJ, Kim D, Baek HS, Cho MH

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Incidentally detected bilateral sub-internal limiting membrane hemorrhages in typical hemolytic uremic syndrome: a case report

Kwon HJ, Song JY

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2025 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr