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Article

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

Journal of the American Society of Nephrology : JASN - 1 Jul 2002

Carraro Michele, Caridi Gianluca, Bruschi Maurizio, Artero Mary, Bertelli Roberta, Zennaro Cristina, Musante Luca, Candiano Giovanni, Perfumo Francesco, Ghiggeri Gian Marco

Abstract excerpt

A plasma factor displaying permeability activity in vitro and possibly determining proteinuria has been hypothesized in idiopathic focal segmental glomerulosclerosis (FSGS). In vitro permeability activity (P(alb)) was determined in sera of five patients with autosomal recessive steroid-resistant nephrotic syndrome (NPHS2), an inherited condition indistinguishable from idiopathic FSGS on clinical grounds, but in...

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Share to Intracellular Signaling Peptides and Proteins
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 12089392
DOI: 10.1097/01.asn.0000016445.29513.ab

Genes

NPHS2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Click a neighbor to travelStep 1 · 12 closest

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome.PMID 12089392Read ↗

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.Semantic proximity Read ↗

Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis.Semantic proximity Read ↗

[Therapeutic apheresis in idiopathic nephrotic syndrome].Semantic proximity Read ↗

Podocin-related mechanisms in posttransplant [corrected] recurrence of focal segmental glomerulosclerosis [corrected].Semantic proximity Read ↗

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.Semantic proximity Read ↗

Plasmapheresis-induced clinical improvement in a patient with steroid-resistant nephrotic syndrome due to podocin (NPHS2) gene mutation.Semantic proximity Read ↗

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.Semantic proximity Read ↗

Post-Transplant Recurrence of Focal Segmental Glomerulosclerosis in a Child With Heterozygous Mutations in NPHS1 and NPHS2.Semantic proximity Read ↗

Recurrence of proteinuria following renal transplantation in congenital nephrotic syndrome of the Finnish type.Semantic proximity Read ↗

Posttransplant recurrence of proteinuria in a case of focal segmental glomerulosclerosis associated with WT1 mutation.Semantic proximity Read ↗

Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus.Semantic proximity Read ↗

NPHS2 mutation associated with recurrence of proteinuria after transplantation.Semantic proximity Read ↗

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