about
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractRenal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locusThe Italian Society for Pediatric Nephrology (SINePe) consensus document on the management of nephrotic syndrome in children: Part I - Diagnosis and treatment of the first episode and the first relapseHemolytic-uremic syndrome as a presenting form of acute lymphocytic leukemia.Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvement.Genetic risk factors in typical haemolytic uraemic syndrome.Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic SyndromeA novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.Broadening the spectrum of diseases related to podocin mutations.COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.Extracorporeal photochemotherapy: a new therapeutic approach for allograft rejection.Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppressionShort-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial.Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trialRituximab in children with resistant idiopathic nephrotic syndrome.Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial.Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations.The effect of donor/recipient body surface area ratio on outcomes in pediatric kidney transplantation.Automated peritoneal dialysis-related peritonitis due to Salmonella enteritidis in a pediatric patient.Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database.Blood pressure measurement in children: which method? which is the gold standard.Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage.Lessons from genetics: is it time to revise the therapeutic approach to children with steroid-resistant nephrotic syndrome?The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.Renal transplantation in sensitized children and young adults: a nationwide approach.Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome.Viral load of EBV DNAemia is a predictor of EBV-related post-transplant lymphoproliferative disorders in pediatric renal transplant recipients.Corticosteroid-free Kidney Transplantation Improves Growth: 2-Year Follow-up of the TWIST Randomized Controlled Trial.Usefulness of 99mTc-dimercaptosuccinic acid renal scan in the diagnosis and follow-up of acute tubulointerstitial nephritis in children.Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds.Near-infrared spectroscopy as continuous real-time monitoring for kidney graft perfusion.Lupus nephritis in children and adolescents: results of the Italian Collaborative Study.Mutational spectrum of the CTNS gene in Italy.Three-yr safety and efficacy of everolimus and low-dose cyclosporine in de novo pediatric kidney transplant patients.Selective decrease in urinary aquaporin 2 and increase in prostaglandin E2 excretion is associated with postobstructive polyuria in human congenital hydronephrosis.One-year results of basiliximab induction and tacrolimus associated with sequential steroid and MMF treatment in pediatric kidney transplant recipient.Peritoneal dialysis in infants: the experience of the Italian Registry of Paediatric Chronic Dialysis.Plasmapheresis-resistant acute humoral rejection successfully treated with anti-C5 antibody.Investigation of intrarenal viral infections in kidney transplant recipients unveils an association between parvovirus B19 and chronic allograft injury.
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P50
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հետազոտող
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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Luisa Murer
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P1153
7004133262
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0000-0002-3010-2337