List of works - Francesco Scolari

A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.

scientific article published on 14 May 2009

Active Focal Segmental Glomerulosclerosis Is Associated with Massive Oxidation of Plasma Albumin

scientific article published on 07 February 2007

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

article

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

scientific article

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 01 April 2019

Autoimmunity in membranous nephropathy targets aldose reductase and SOD2.

scientific article

Broadening the spectrum of diseases related to podocin mutations

scientific article

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

scientific article published on 30 April 2009

Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy.

scientific article

Copy-number disorders are a common cause of congenital kidney malformations

scientific article

Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study

scientific article published on September 2004

Depletion of clusterin in renal diseases causing nephrotic syndrome

Determination of the oxido-redox status of plasma albumin in hemodialysis patients.

scientific article published on 31 January 2008

Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens.

scientific article

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

scientific article

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

article

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

scientific article

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

scientific article

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

scientific article

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens.

scientific article

Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI.

scientific article

Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33

scientific article published on 26 January 2007

New iodo-acetamido cyanines for labeling cysteine thiol residues. A strategy for evaluating plasma proteins and their oxido-redox status

scientific article published in January 2009

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood

Proteins and protein fragments in nephrotic syndrome: Clusters, specificity and mechanisms

scientific article published on 18 June 2008

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

scientific article published in January 2006

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

scientific article

Renal outcome in patients with congenital anomalies of the kidney and urinary tract.

scientific article

Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome.

scientific article

Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome

scientific article published on 05 June 2013

Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: protocol of a pilot randomised controlled trial

scientific article published on 04 December 2019

Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: protocol of a pilot randomised controlled trial

scientific article published in 2019

Urinary secretion and extracellular aggregation of mutant uromodulin isoforms.

scientific article published on 11 January 2012

Uromodulin storage diseases: clinical aspects and mechanisms

scientific article

List of works by Francesco Scolari

A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.

Active Focal Segmental Glomerulosclerosis Is Associated with Massive Oxidation of Plasma Albumin

Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Autoimmunity in membranous nephropathy targets aldose reductase and SOD2.

Broadening the spectrum of diseases related to podocin mutations

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

Coexistence of different circulating anti-podocyte antibodies in membranous nephropathy.

Copy-number disorders are a common cause of congenital kidney malformations

Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study

Depletion of clusterin in renal diseases causing nephrotic syndrome

Determination of the oxido-redox status of plasma albumin in hemodialysis patients.

Direct characterization of target podocyte antigens and auto-antibodies in human membranous glomerulonephritis: Alfa-enolase and borderline antigens.

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

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

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Glomerular Autoimmune Multicomponents of Human Lupus Nephritis In Vivo (2): Planted Antigens.

Glomerular autoimmune multicomponents of human lupus nephritis in vivo: α-enolase and annexin AI.

Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33

New iodo-acetamido cyanines for labeling cysteine thiol residues. A strategy for evaluating plasma proteins and their oxido-redox status

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood

Proteins and protein fragments in nephrotic syndrome: Clusters, specificity and mechanisms

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 outcome in patients with congenital anomalies of the kidney and urinary tract.

Repetitive fragmentation products of albumin and alpha1-antitrypsin in glomerular diseases associated with nephrotic syndrome.

Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome

Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: protocol of a pilot randomised controlled trial

Rituximab versus steroids and cyclophosphamide for the treatment of primary membranous nephropathy: protocol of a pilot randomised controlled trial

Urinary secretion and extracellular aggregation of mutant uromodulin isoforms.

Uromodulin storage diseases: clinical aspects and mechanisms