Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The primary hyperoxalurias.

Kidney international - 1 Jun 2009

Hoppe Bernd, Beck Bodo B, Milliner Dawn S

Abstract excerpt

The primary hyperoxalurias (PHs) are rare disorders of glyoxylate metabolism in which specific hepatic enzyme deficiencies result in overproduction of oxalate. Due to the resulting severe hyperoxaluria, recurrent urolithiasis or progressive nephrocalcinosis are principal manifestations. End stage renal failure frequently occurs and is followed by systemic oxalate deposition along with its devastating effects. Due...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Pyridoxine
Share to Transaminases
Share to Alcohol Oxidoreductases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperoxaluria, Primary

Share to Kidney Failure, Chronic

Share to Kidney Transplantation

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 19225556
DOI: 10.1038/ki.2009.32
PMCID: PMC4577278

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

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The primary hyperoxalurias.PMID 19225556Read ↗

An update on primary hyperoxaluria.Semantic proximity Read ↗

A molecular journey on the pathogenesis of primary hyperoxaluria.Semantic proximity Read ↗

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.Semantic proximity Read ↗

Primary HyperoxaluriaSemantic proximity Read ↗

Primary hyperoxaluria: spectrum of clinical and imaging findings.Semantic proximity Read ↗

Primary hyperoxalurias: diagnosis and treatment.Semantic proximity Read ↗

[Primary hyperoxaluria].Semantic proximity Read ↗

Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.Semantic proximity Read ↗

[Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder].Semantic proximity Read ↗

Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center.Semantic proximity Read ↗

Molecular Aetiology of Primary Hyperoxaluria Type 1Semantic proximity Read ↗

Phenotypic expression of primary hyperoxaluria: comparative features of types I and II.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.