Lista de obras - Luisa Murer - Dominio Público Uruguay

10p12.1 deletion: HDR phenotype without DGS2 features

artículo científico publicado en 2008

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis

artículo científico publicado en 2010

A propensity-matched comparison of hard outcomes in children on chronic dialysis.

artículo científico publicado en 2017

Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trial

artículo científico publicado en 2007

Automated peritoneal dialysis-related peritonitis due to Salmonella enteritidis in a pediatric patient

artículo científico

Benefits of photopheresis in the treatment of heart transplant patients with multiple/refractory rejection

artículo científico publicado en 1997

Blood pressure measurement in children: which method? which is the gold standard.

artículo científico

Broadening the spectrum of diseases related to podocin mutations

artículo científico publicado en 2003

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

artículo científico publicado en 2007

CVVHD treatment with CARPEDIEM: small solute clearance at different blood and dialysate flows with three different surface area filter configurations.

artículo científico publicado en 2016

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome

artículo científico publicado en 2015

Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: Insights from molecular screening

article

Clinical and molecular markers of chronic interstitial nephropathy in congenital unilateral ureteropelvic junction obstruction.

artículo científico publicado en 2006

Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations

artículo científico publicado en 2009

Clinico-pathological correlation in duplex system ectopic ureters and ureteroceles: can preoperative work-up predict renal histology?

artículo científico publicado en 2011

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN.

artículo científico publicado en 2017

Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome

artículo científico publicado en 2016

Corticosteroid-free Kidney Transplantation Improves Growth: 2-Year Follow-up of the TWIST Randomized Controlled Trial.

artículo científico publicado en 2015

Delayed graft function in pediatric deceased donor kidney transplantation: Donor-related risk factors and impact on two-yr graft function and survival: A single-center analysis

artículo científico publicado en 2014

Detection of Viral DNA in Kidney Graft Preservation and Washing Solutions Is Predictive of Posttransplant Infections in Pediatric Recipients

scientific article published on 01 November 2009

Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvement

artículo científico publicado en 2008

Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia.

artículo científico publicado en 2007

Encapsulating peritoneal sclerosis in paediatric peritoneal dialysis patients: the experience of the Italian Registry of Pediatric Chronic Dialysis

article

Erratum to: Viral load of EBV DNAemia is a predictor of EBV-related post-transplant lymphoproliferative disorders in pediatric renal transplant recipients

artículo científico publicado en 2017

Expression of Nuclear Transcription Factor PAX2 in Renal Biopsies of Juvenile Nephronophthisis

artículo científico publicado en 2002

Extracorporeal photochemotherapy: a new therapeutic approach for allograft rejection.

artículo científico publicado en 2002

Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds

artículo científico publicado en 2005

Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants

artículo científico publicado en 2017

Genetic risk factors in typical haemolytic uraemic syndrome

artículo científico publicado en 2008

Hemolytic-uremic syndrome as a presenting form of acute lymphocytic leukemia.

artículo científico publicado en 2000

Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression

artículo científico publicado en 2014

Immature Renal Structures Associated With a Novel UMOD Sequence Variant

Immunohistochemical Distribution of Endothelin in Biopsies of Pediatric Nephrotic Syndrome

artículo científico publicado en 1994

Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.

artículo científico publicado en 2005

Interleukin-8 and CXCR1 Receptor Functional Polymorphisms and Susceptibility to Acute Pyelonephritis

artículo científico publicado en 2007

Investigation of intrarenal viral infections in kidney transplant recipients unveils an association between parvovirus B19 and chronic allograft injury.

artículo científico publicado en 2009

Kidney transplantation into bladder augmentation or urinary diversion: long-term results.

artículo científico publicado en 2005

Lessons from genetics: is it time to revise the therapeutic approach to children with steroid-resistant nephrotic syndrome?

artículo científico publicado en 2016

Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children.

artículo científico publicado en 2017

Long-term treatment with CsA decreases INF-gamma mRNA and increases pre-pro-ET-1 mRNA in rat kidneys

artículo científico publicado en 1998

Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variables

artículo científico publicado en 2009

Lower urinary tract symptoms (LUTS) after renal transplant in non-urologic anuric patients

artículo científico publicado en 2010

Lupus nephritis in children and adolescents: results of the Italian Collaborative Study

artículo científico publicado en 2013

Mutational spectrum of the CTNS gene in Italy

artículo científico publicado en 2003

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract

artículo científico publicado en 2010

Mycophenolate mofetil pharmacokinetic monitoring in pediatric kidney transplant recipients

artículo científico publicado en 2005

Near-infrared spectroscopy as continuous real-time monitoring for kidney graft perfusion

artículo científico publicado en 2013

Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the association

artículo científico publicado en 2006

One-year results of basiliximab induction and tacrolimus associated with sequential steroid and MMF treatment in pediatric kidney transplant recipient

artículo científico publicado en 2005

Outcome of childhood-onset full-house nephropathy.

artículo científico publicado en 2017

Outcome of renal transplantation in small infants: a match-controlled analysis.

artículo científico publicado en 2018

PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomalies

article

Peritoneal dialysis in infants: the experience of the Italian Registry of Paediatric Chronic Dialysis.

artículo científico publicado en 2011

Pharmacokinetic of cyclosporine microemulsion in pediatric kidney recipients receiving A quadruple immunosuppressive regimen: the value of C2 blood levels

artículo científico publicado en 2005

Phenotypic and genetic heterogeneity in Dent's disease—the results of an Italian collaborative study

article

Plasmapheresis-resistant acute humoral rejection successfully treated with anti-C5 antibody

artículo científico publicado en 2013

Primary Intrarenal Posttransplant Lymphoproliferative Disorder Detected by Surveillance Protocol Biopsy

artículo científico publicado en 2012

Rapid determination of creatinine in serum and urine by ion-pair high-performance liquid chromatography

artículo científico publicado en 1999

Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.

artículo científico publicado en 2006

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin

artículo científico publicado en 2003

Renal hypoplasia without optic coloboma associated with PAX2 gene deletion

article

Renal transplantation in children weighing <15 kg: does concomitant lower urinary tract dysfunction influence the outcome?

artículo científico publicado en 2015

Renal transplantation in sensitized children and young adults: a nationwide approach

artículo científico publicado en 2016

Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus

artículo científico publicado en 1998

Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome

scientific article published on 12 December 2019

Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial

artículo científico publicado en 2015

Rituximab in children with resistant idiopathic nephrotic syndrome

artículo científico publicado en 2012

SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract

article

Selective decrease in urinary aquaporin 2 and increase in prostaglandin E2 excretion is associated with postobstructive polyuria in human congenital hydronephrosis.

artículo científico publicado en 2004

Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial

artículo científico publicado en 2011

Significance of serial biopsies after renal allograft in children

artículo científico publicado en 1998

Successful renal transplantation in children under 6 years of age

artículo científico publicado en 2001

TGFbeta1 induces epithelial-mesenchymal transition, but not myofibroblast transdifferentiation of human kidney tubular epithelial cells in primary culture.

artículo científico publicado en 2006

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

artículo científico publicado en 2017

The effect of donor/recipient body surface area ratio on outcomes in pediatric kidney transplantation.

artículo científico publicado en 2008

The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis

artículo científico publicado en 2017

The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults.

artículo científico publicado en 2009

The pharmacokinetics and immunosuppressive response of tacrolimus in paediatric renal transplant recipients

artículo científico publicado en 2006

Therapeutic Plasma Exchange in Neonates and Infants: Successful Use of a Miniaturized Machine

scholarly article by Enrico Vidal et al published 2017 in Blood Purification

Three-yr safety and efficacy of everolimus and low-dose cyclosporine in de novo pediatric kidney transplant patients.

artículo científico publicado en 2014

Transplant renal artery stenosis in children: risk factors and outcome after endovascular treatment.

artículo científico publicado en 2013

Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus-specific database.

artículo científico publicado en 2012

Upper Urinary Tract Infections Are Associated with RANTES Promoter Polymorphism

artículo científico publicado en 2010

Ureteral complications after renal transplant in children: timing of presentation, and their open and endoscopic management

artículo científico publicado en 2013

Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damage

artículo científico

Use of Rituximab in Focal Glomerulosclerosis Relapses After Renal Transplantation

scientific article published on 01 August 2009

Usefulness of 99mTc-dimercaptosuccinic acid renal scan in the diagnosis and follow-up of acute tubulointerstitial nephritis in children.

artículo científico publicado en 2017

Viral load of EBV DNAemia is a predictor of EBV-related post-transplant lymphoproliferative disorders in pediatric renal transplant recipients.

artículo científico publicado en 2017

mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis

scientific article published on 01 July 2014

Lista de obras de Luisa Murer

10p12.1 deletion: HDR phenotype without DGS2 features

A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis

A propensity-matched comparison of hard outcomes in children on chronic dialysis.

Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trial

Automated peritoneal dialysis-related peritonitis due to Salmonella enteritidis in a pediatric patient

Benefits of photopheresis in the treatment of heart transplant patients with multiple/refractory rejection

Blood pressure measurement in children: which method? which is the gold standard.

Broadening the spectrum of diseases related to podocin mutations

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

CVVHD treatment with CARPEDIEM: small solute clearance at different blood and dialysate flows with three different surface area filter configurations.

Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome

Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: Insights from molecular screening

Clinical and molecular markers of chronic interstitial nephropathy in congenital unilateral ureteropelvic junction obstruction.

Clinical features and long-term outcome of nephrotic syndrome associated with heterozygous NPHS1 and NPHS2 mutations

Clinico-pathological correlation in duplex system ectopic ureters and ureteroceles: can preoperative work-up predict renal histology?

Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GN.

Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome

Corticosteroid-free Kidney Transplantation Improves Growth: 2-Year Follow-up of the TWIST Randomized Controlled Trial.

Delayed graft function in pediatric deceased donor kidney transplantation: Donor-related risk factors and impact on two-yr graft function and survival: A single-center analysis

Detection of Viral DNA in Kidney Graft Preservation and Washing Solutions Is Predictive of Posttransplant Infections in Pediatric Recipients

Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvement

Embryology and genetics of primary vesico-ureteric reflux and associated renal dysplasia.

Encapsulating peritoneal sclerosis in paediatric peritoneal dialysis patients: the experience of the Italian Registry of Pediatric Chronic Dialysis

Erratum to: Viral load of EBV DNAemia is a predictor of EBV-related post-transplant lymphoproliferative disorders in pediatric renal transplant recipients

Expression of Nuclear Transcription Factor PAX2 in Renal Biopsies of Juvenile Nephronophthisis

Extracorporeal photochemotherapy: a new therapeutic approach for allograft rejection.

Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindreds

Further phenotypic heterogeneity of CoQ10 deficiency associated with steroid resistant nephrotic syndrome and novel COQ2 and COQ6 variants

Genetic risk factors in typical haemolytic uraemic syndrome

Hemolytic-uremic syndrome as a presenting form of acute lymphocytic leukemia.

Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression

Immature Renal Structures Associated With a Novel UMOD Sequence Variant

Immunohistochemical Distribution of Endothelin in Biopsies of Pediatric Nephrotic Syndrome

Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.

Interleukin-8 and CXCR1 Receptor Functional Polymorphisms and Susceptibility to Acute Pyelonephritis

Investigation of intrarenal viral infections in kidney transplant recipients unveils an association between parvovirus B19 and chronic allograft injury.

Kidney transplantation into bladder augmentation or urinary diversion: long-term results.

Lessons from genetics: is it time to revise the therapeutic approach to children with steroid-resistant nephrotic syndrome?

Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children.

Long-term treatment with CsA decreases INF-gamma mRNA and increases pre-pro-ET-1 mRNA in rat kidneys

Longitudinal evaluation of mycophenolic acid pharmacokinetics in pediatric kidney transplant recipients. The role of post-transplant clinical and therapeutic variables

Lower urinary tract symptoms (LUTS) after renal transplant in non-urologic anuric patients

Lupus nephritis in children and adolescents: results of the Italian Collaborative Study

Mutational spectrum of the CTNS gene in Italy

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract

Mycophenolate mofetil pharmacokinetic monitoring in pediatric kidney transplant recipients

Near-infrared spectroscopy as continuous real-time monitoring for kidney graft perfusion

Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the association

One-year results of basiliximab induction and tacrolimus associated with sequential steroid and MMF treatment in pediatric kidney transplant recipient

Outcome of childhood-onset full-house nephropathy.

Outcome of renal transplantation in small infants: a match-controlled analysis.

PAX2 gene mutations in pediatric and young adult transplant recipients: kidney and urinary tract malformations without ocular anomalies

Peritoneal dialysis in infants: the experience of the Italian Registry of Paediatric Chronic Dialysis.

Pharmacokinetic of cyclosporine microemulsion in pediatric kidney recipients receiving A quadruple immunosuppressive regimen: the value of C2 blood levels

Phenotypic and genetic heterogeneity in Dent's disease—the results of an Italian collaborative study

Plasmapheresis-resistant acute humoral rejection successfully treated with anti-C5 antibody

Primary Intrarenal Posttransplant Lymphoproliferative Disorder Detected by Surveillance Protocol Biopsy

Rapid determination of creatinine in serum and urine by ion-pair high-performance liquid chromatography

Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin

Renal hypoplasia without optic coloboma associated with PAX2 gene deletion

Renal transplantation in children weighing <15 kg: does concomitant lower urinary tract dysfunction influence the outcome?

Renal transplantation in sensitized children and young adults: a nationwide approach

Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus

Reverse Phenotyping after Whole-Exome Sequencing in Steroid-Resistant Nephrotic Syndrome

Rituximab in Children with Steroid-Dependent Nephrotic Syndrome: A Multicenter, Open-Label, Noninferiority, Randomized Controlled Trial

Rituximab in children with resistant idiopathic nephrotic syndrome

SIX1 gene: absence of mutations in children with isolated congenital anomalies of kidney and urinary tract

Selective decrease in urinary aquaporin 2 and increase in prostaglandin E2 excretion is associated with postobstructive polyuria in human congenital hydronephrosis.

Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: a randomized controlled trial

Significance of serial biopsies after renal allograft in children

Successful renal transplantation in children under 6 years of age

TGFbeta1 induces epithelial-mesenchymal transition, but not myofibroblast transdifferentiation of human kidney tubular epithelial cells in primary culture.

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

The effect of donor/recipient body surface area ratio on outcomes in pediatric kidney transplantation.

The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis

The impact of eNOS, MTR and MTHFR polymorphisms on renal graft survival in children and young adults.

The pharmacokinetics and immunosuppressive response of tacrolimus in paediatric renal transplant recipients

Therapeutic Plasma Exchange in Neonates and Infants: Successful Use of a Miniaturized Machine