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SPECIAL ARTICLE 2019 October 30
Primary Hyperoxaluria in Korean Pediatric Patients
Background: Primary hyperoxaluria (PH), a rare inborn error of glyoxylate meta bolism causing overproduction of oxalate, is classified into three genetic subgroups: type 13 (PH1밣H3) caused by AGXT, GRHPR, and HOGA1 gene mutations, respectively. We perfo...
SPECIAL ARTICLE 2019 October 30
Cell-derived Secretome for the Treatment of Renal Disease
Kidney disease is a major global health issue. Hemodialysis and kidney transplantation have been used in the clinic to treat renal failure. However, the dialysis is not an effective long-term option, as it is unable to replace complete renal functions. Kidney transplantation is ...
ORIGINAL ARTICLE 2019 October 30
The associations of Urinary Neutrophil Gelatinase-associated Lipocalin (NGAL) and Liver-type Fatty Acid Binding Protein (L-FABP) Levels with Hematuria in Children and Adolescents
Purpose: We sought to determine associations of urinary neutrophil gelatinase-associated lipocalin (NGAL) and liver-type fatty acid-binding protein (L-FABP), known markers of renal injury, with hematuria in children and adolescents. Methods: A total of 112 urine samples from 72 ...
CASE REPORT 2019 October 30
Vitamin D Dependent Rickets Type 1A Caused by CYP27B1 Mutation
Vitamin D dependent rickets type 1A (VDDR1A) is an autosomal recessive disorder caused by mutations in CYP27B1 . Clinical findings are growth retardation, hypotonia, muscle weakness, hypocalcemic seizures, and radiological features of rickets. We aimed to present the VDDR...
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eISSN : 2384-0250
pISSN : 2384-0242
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Volume 23(2); October 2019
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