Lista de obras -

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

artículo científico publicado en 2003

Broadening the spectrum of diseases related to podocin mutations

artículo científico publicado en 2003

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

artículo científico publicado en 2004

Depletion of clusterin in renal diseases causing nephrotic syndrome

Familial forms of nephrotic syndrome.

artículo científico publicado en 2010

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

artículo científico publicado en 2007

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Glomerular albumin permeability as anin vitromodel for characterizing the mechanism of focal glomerulosclerosis and predicting post-transplant recurrence

Glomerulocystic kidney disease in a family

artículo científico publicado en 2002

Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria

article

Lack of cardiac anomalies in children with NPHS2 mutations

artículo científico publicado en 2007

Protracted remission of proteinuria after combined therapy with plasmapheresis and anti-CD20 antibodies/cyclophosphamide in a child with oligoclonal IgM and glomerulosclerosis

artículo científico publicado en 2007

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

Recurrent lymphomatoid papulosis associated with nephrotic syndrome. An occurrence of uncertain origin

artículo científico publicado en 2007

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

artículo científico publicado en 2006

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome

artículo científico publicado en 2002

Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy

article

Transitions of serum albumin in patients with glomerulosclerosis ‘in vivo’ characterization by electrophoretic titration curves

artículo científico publicado en 2006

Lista de obras de

Apolipoprotein E in idiopathic nephrotic syndrome and focal segmental glomerulosclerosis.

Broadening the spectrum of diseases related to podocin mutations

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

Depletion of clusterin in renal diseases causing nephrotic syndrome

Familial forms of nephrotic syndrome.

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Genetic approaches to human renal agenesis/hypoplasia and dysplasia

Glomerular albumin permeability as anin vitromodel for characterizing the mechanism of focal glomerulosclerosis and predicting post-transplant recurrence

Glomerulocystic kidney disease in a family

Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria

Lack of cardiac anomalies in children with NPHS2 mutations

Protracted remission of proteinuria after combined therapy with plasmapheresis and anti-CD20 antibodies/cyclophosphamide in a child with oligoclonal IgM and glomerulosclerosis

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

Recurrent lymphomatoid papulosis associated with nephrotic syndrome. An occurrence of uncertain origin

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

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome

Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy

Transitions of serum albumin in patients with glomerulosclerosis ‘in vivo’ characterization by electrophoretic titration curves

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes