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

Primary hyperoxalurias: diagnosis and treatment.

Pediatric nephrology (Berlin, Germany) - 1 Oct 2015

Ben-Shalom Efrat, Frishberg Yaacov

Abstract excerpt

Primary hyperoxalurias (PH) comprise a group of three distinct metabolic diseases caused by derangement of glyoxylate metabolism in the liver. Recent years have seen advances in several aspects of PH research. This paper reviews current knowledge of the genetic and biochemical basis of PH, the specific epidemiology and clinical presentation of each type, and therapeutic approaches in different disease stages....

Read the complete abstract on PubMed

Topics

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

Share to Genetic Predisposition to Disease
Share to Genetic Testing
Share to Hyperoxaluria, Primary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Nephrolithiasis

Share to Transaminases

Source

Identifiers

PMID: 25519509
DOI: 10.1007/s00467-014-3030-1

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Primary hyperoxalurias: diagnosis and treatment.PMID 25519509Read ↗

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

The primary hyperoxalurias.Semantic proximity Read ↗

A molecular journey on the pathogenesis of primary hyperoxaluria.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 ↗

Primary HyperoxaluriaSemantic proximity Read ↗

Molecular Aetiology of Primary Hyperoxaluria Type 1Semantic proximity Read ↗

Molecular insights into primary hyperoxaluria Type I pathogenesisSemantic proximity Read ↗

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

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

Molecular etiology of primary hyperoxaluria type 1: new directions for treatment.Semantic proximity Read ↗

Molecular aetiology of primary hyperoxaluria and its implications for clinical management.Semantic proximity Read ↗

An update on primary hyperoxaluria.Semantic proximity Read ↗

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