Ion chromatography (IC) plays a crucial role in urine analysis for diverse medical diagnoses.
This paper reviews a comprehensive investigation into urine pretreatment techniques, as …

Purpose Primary hyperoxaluria type 1 (PH1) is a rare, progressive, genetic disease with
limited treatment options. We report the efficacy and safety of lumasiran, an RNA …

Background. Primary hyperoxaluria type 1 (PH1) is a phenotypically heterogeneous
disease. To date the relationship between biochemical parameters and outcome is unclear …

The clinical presentation of primary hyperoxaluria in children ranges from mildly
symptomatic nephrocalcinosis to very early onset end-stage kidney failure with systemic …

Background Primary hyperoxaluria type 1 (PH1) is a rare genetic disease that causes
progressive kidney damage and systemic oxalosis due to hepatic overproduction of oxalate …

Purpose The continued evolution of stone treatment modalities, such as endourologic
procedures, open surgery and shock wave lithotripsy, makes the assessment of continuous …

Purpose: Pediatric urolithiasis is relatively uncommon and there is little information on the
application of modern surgical procedures in young children. We present a single center …

A random urine calcium/creatinine ratio (UCa/Cr) is of practical use in screening for
hypercalciuria. However, due to worldwide variations, reference values for the pediatric …

Objectives: Urolithiasis in children is recognized with an increasing frequency, while exact
etiological factors remain to be determined. The aim of this study is to compare the metabolic …

Given the wide diversity of causes of hematuria, ranging from simple urinary tract infections
with rapid recovery to severe glomerulonephritis with fast decline in kidney function, it is …