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Article

[Genotype-phenotype correlation in ADPKD: a possible role for NGAL?].

Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia - 1 Jan 2000

Virzì Grazia Maria, Gastaldon Fiorella, Corradi Valentina, de Cal Massimo, Cruz Dinna N, Clementi Maurizio, Ronco Claudio

Abstract excerpt

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic cause of chronic kidney disease (CKD) in adults. It is associated with both inter- and intra- familial variability, which can be explained by genetic heterogeneity, modifier genes and a genetic background. NGAL, a 25-kDa protein released from tubular cells after harmful stimuli, is a new biomarker. Recent studies suggest a...

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Source

Identifiers

PMID: 24941494

Genes

PKD2
PKD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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