Pages that link to "Q44237018"
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The following pages link to Luisa Murer (Q44237018):
Displaying 50 items.
- Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract (Q24304067) (← links)
- Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus (Q28291661) (← links)
- The 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 relapse (Q29994584) (← links)
- Hemolytic-uremic syndrome as a presenting form of acute lymphocytic leukemia. (Q33334080) (← links)
- Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvement (Q33382393) (← links)
- Genetic risk factors in typical haemolytic uraemic syndrome (Q33382580) (← links)
- Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome (Q33421800) (← links)
- A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis (Q33769998) (← links)
- Broadening the spectrum of diseases related to podocin mutations (Q34192029) (← links)
- COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement (Q34687106) (← links)
- Extracorporeal photochemotherapy: a new therapeutic approach for allograft rejection. (Q34748805) (← links)
- Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression (Q34787771) (← links)
- Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial (Q35030581) (← links)
- Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin (Q35140901) (← links)
- Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trial (Q35955129) (← links)
- Rituximab in children with resistant idiopathic nephrotic syndrome (Q35982341) (← links)
- Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial (Q36003160) (← links)
- Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations (Q37211071) (← links)
- The effect of donor/recipient body surface area ratio on outcomes in pediatric kidney transplantation. (Q37344991) (← links)
- Automated peritoneal dialysis-related peritonitis due to Salmonella enteritidis in a pediatric patient (Q37941492) (← links)
- Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database. (Q37972823) (← links)
- Blood pressure measurement in children: which method? which is the gold standard. (Q38087915) (← links)
- Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage (Q38457820) (← links)
- Lessons from genetics: is it time to revise the therapeutic approach to children with steroid-resistant nephrotic syndrome? (Q38840895) (← links)
- The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis (Q38944507) (← links)
- Renal transplantation in sensitized children and young adults: a nationwide approach (Q39289605) (← links)
- Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome (Q39983750) (← links)
- Viral load of EBV DNAemia is a predictor of EBV-related post-transplant lymphoproliferative disorders in pediatric renal transplant recipients. (Q40298660) (← links)
- Corticosteroid-free Kidney Transplantation Improves Growth: 2-Year Follow-up of the TWIST Randomized Controlled Trial. (Q41582647) (← links)
- Usefulness of 99mTc-dimercaptosuccinic acid renal scan in the diagnosis and follow-up of acute tubulointerstitial nephritis in children. (Q41955483) (← links)
- Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds (Q42653487) (← links)
- Near-infrared spectroscopy as continuous real-time monitoring for kidney graft perfusion (Q44063607) (← links)
- Lupus nephritis in children and adolescents: results of the Italian Collaborative Study (Q44236946) (← links)
- Mutational spectrum of the CTNS gene in Italy (Q44490436) (← links)
- Three-yr safety and efficacy of everolimus and low-dose cyclosporine in de novo pediatric kidney transplant patients. (Q44522008) (← links)
- Selective decrease in urinary aquaporin 2 and increase in prostaglandin E2 excretion is associated with postobstructive polyuria in human congenital hydronephrosis. (Q45091485) (← links)
- One-year results of basiliximab induction and tacrolimus associated with sequential steroid and MMF treatment in pediatric kidney transplant recipient (Q45197114) (← links)
- Peritoneal dialysis in infants: the experience of the Italian Registry of Paediatric Chronic Dialysis. (Q45596034) (← links)
- Plasmapheresis-resistant acute humoral rejection successfully treated with anti-C5 antibody (Q45736192) (← links)
- Investigation of intrarenal viral infections in kidney transplant recipients unveils an association between parvovirus B19 and chronic allograft injury. (Q45925879) (← links)
- The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults. (Q46059628) (← links)
- Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variables (Q46134304) (← links)
- Mycophenolate mofetil pharmacokinetic monitoring in pediatric kidney transplant recipients (Q46452789) (← links)
- Pharmacokinetic of cyclosporine microemulsion in pediatric kidney recipients receiving A quadruple immunosuppressive regimen: the value of C2 blood levels (Q46478188) (← links)
- Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition. (Q46664045) (← links)
- Ureteral complications after renal transplant in children: timing of presentation, and their open and endoscopic management (Q46727809) (← links)
- A propensity-matched comparison of hard outcomes in children on chronic dialysis. (Q47587328) (← links)
- Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN. (Q47650832) (← links)
- Erratum to: Viral load of EBV DNAemia is a predictor of EBV-related post-transplant lymphoproliferative disorders in pediatric renal transplant recipients (Q47713860) (← links)
- Significance of serial biopsies after renal allograft in children (Q47939985) (← links)