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

[Biochemical and molecular diagnosis of primary hyperoxaluria type 1: Tunisian study about 15 cases].

Pathologie-biologie - 1 Aug 2011

Belhaj R, Hayder N, Gargueh T, Zorguati M, Marrakchi O, Abdelhak S, Lakhoua R, Abdelmoula J

Abstract excerpt

BACKGROUND: The primary type 1 hyperoxaluria (HP1) is the most frequent and severe form of the primary hyperoxaluriae. It is related to an enzymatic deficit in alanine glyoxylate aminotransferase (AGT). It is a recessive autosomic disease. Rare in Europe, it is responsible for 13% of the end stage renal failure in the Tunisian child. AIM: The aim of this work is to evaluate the biological and molecular...

Read the complete abstract on PubMed

Topics

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

Share to Calcium
Share to Consanguinity
Share to Crystallization

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hyperoxaluria, Primary

Share to Infant

Share to Transaminases

Share to Tunisia

Share to Urinary Calculi

Source

Identifiers

PMID: 19896299
DOI: 10.1016/j.patbio.2009.05.009

Genes

AGT
AGXT

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Biochemical and molecular diagnosis of primary hyperoxaluria type 1: Tunisian study about 15 cases].PMID 19896299Read ↗

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

[Genetic aspects of primary hyperoxaluria: diagnostics and treatment].Semantic proximity Read ↗

[Primary hyperoxaluria].Semantic proximity Read ↗

Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa.Semantic proximity Read ↗

Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I.Semantic proximity Read ↗

Unusual clinical outcome of primary Hyperoxaluria type 1 in Tunisian patients carrying 33_34InsC mutation.Semantic proximity Read ↗

Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.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 Analysis of the AGXT Gene Detected a Missense and Pathogenic Variant Associated with Primary Hyperoxaluria Type 1; a Case StudySemantic proximity Read ↗

Mutational analysis of AGXT gene in Libyan children with primary hyperoxaluria type 1 at Tripoli Children Hospital.Semantic proximity Read ↗

Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria.Semantic proximity Read ↗

An update on primary hyperoxaluria.Semantic proximity Read ↗

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