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Phosphate transporters, candidate genes, and the prosecutor’s fallacy
doi : 10.1007/s00467-025-06660-1
Volume 40, Issue 6 June 2025
Is there sufficient similarity of glomerular diseases across the life course?
Kidney lipid metabolism: impact on pediatric kidney diseases and modulation by early-life nutrition
Severe maternal undernutrition during pregnancy and its long-term effects on the offspring health, with a focus on kidney health
Advancements of aquaporin 1 in ultrafiltration failure secondary to peritoneal dialysis
Hepatopulmonary syndrome from liver disease associated with autosomal recessive polycystic kidney disease
A case of Sjögren’s syndrome with selective anion exchanger 1 defect causing distal renal tubular acidosis
The beneficial effect of adding belimumab in severe and refractory IgA nephropathy: a case report
Diagnosing alkaptonuria-related nephropathy with urine albumin analysis
De novo proliferative glomerulonephritis with monoclonal IgG deposits in an adolescent kidney transplant recipient
Etiology, clinical characteristics, genetic profile, and outcomes of children with refractory rickets at a referral center in India: a cohort study
Variable treatment response to lumasiran in pediatric patients with primary hyperoxaluria type 1
Nedosiran in pediatric patients with PH1 and relatively preserved kidney function, a phase 2 study (PHYOX8)
Comparing adolescent glomerular disease clinical outcomes to the clinical outcomes in childhood, young adult, and adult-onset glomerular disease in the CureGN database
Efficacy of complement inhibition with pegcetacoplan in children with C3 glomerulopathy
Clinical applicability of 2023 International Pediatric Nephrology Association recommended limited therapeutic drug monitoring formulae to assess mycophenolic acid exposure
Prediction model for severe vesicoureteral reflux in children with urinary tract infection and/or hydronephrosis
Open-label, controlled, phase 2 clinical trial assessing the safety, efficacy, and pharmacokinetics of INM004 in pediatric patients with Shiga toxin-producing Escherichia coli–associated hemolytic uremic syndrome
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40
Model-informed repurposing of eliglustat for treatment and prophylaxis of Shiga toxin-producing Escherichia coli hemolytic-uremic syndrome (STEC-HUS) in children
Utility of shear wave elastography in evaluation of children with chronic kidney disease
A comparison of health-related quality of life between continuous ambulatory peritoneal dialysis and automated peritoneal dialysis in children with stage 5 chronic kidney disease in Thailand: a randomized controlled trial
Survey of legislative frameworks and national recommendations governing paediatric maintenance haemodialysis in Europe
Assessing burden among caregivers of pediatric dialysis and kidney transplant patients
Factors associated with statural growth in pediatric kidney transplant recipients with focus on metabolic acidosis
Relationship between intraoperative blood pressure variability and postoperative acute kidney injury in pediatric cardiac surgery
Experience of continuous kidney replacement therapy in a tertiary care unit of a lower-middle-income country
The incidence of acute kidney injury in very-low-birth-weight infants treated early with caffeine
Exploring the risks of cefepime in acute kidney injury for pediatric and young adult critical care
Shear wave elastography for the evaluation of children with chronic kidney disease: promising, but insufficient
Complexity in assessing acute kidney injury and cefepime exposure in critically ill patients
WE-ROCK and the challenge of global accessibility: are we reaching children worldwide?
Making a start – WE-ROCK registry and the aim of global equity in pediatric CKRT
