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

A C597-->A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in premature Kuwaiti infants.

Journal of biomedical science - 1 Jan 2000

Haider M Z, Devarajan L V, Al-Essa M, Kumar H

Abstract excerpt

Retinopathy of prematurity (ROP) is a retinal vascular disease which occurs in infants with a short gestational age and low birth weight and may lead to retinal detachment and blindness. In some premature infants, ROP progresses to advanced stages despite rigorous intervention, but in the majority, it spontaneously regresses before the threshold stage. Genetic factors, e.g. mutations in the Norrie disease (ND)...

Read the complete abstract on PubMed

Topics

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

Share to Birth Weight
Share to Disease Progression

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

Share to Gestational Age

Share to Incidence

Share to Infant, Premature

Share to Kuwait

Share to Polymorphism, Restriction Fragment Length

Share to Retinopathy of Prematurity

Source

Identifiers

PMID: 12145535
DOI: 10.1007/BF02256593

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

A C597-->A polymorphism in the Norrie disease gene is associated with advanced retinopathy of prematurity in premature Kuwaiti infants.PMID 12145535Read ↗

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.Semantic proximity Read ↗

Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity.Semantic proximity Read ↗

Identification of genetic factors underlying severe retinopathy of prematurity in preterm infants.Semantic proximity Read ↗

Pathogenesis and genetic basis for retinopathy of prematurity.Semantic proximity Read ↗

Genetic susceptibility to advanced retinopathy of prematurity (ROP).Semantic proximity Read ↗

Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematuritySemantic proximity Read ↗

Mutations of the Norrie gene in Korean ROP infants.Semantic proximity Read ↗

Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants.Semantic proximity Read ↗

An Updated and Comprehensive Meta-Analysis of Association between VEGA -634G > C, -460T > C, +405G > C and +936C > T Polymorphisms and Retinopathy of Prematurity Risk.Semantic proximity Read ↗

Endothelial nitric oxide synthase gene T-786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity.Semantic proximity Read ↗

Genetic variation of vascular endothelial growth factor pathway does not correlate with the severity of retinopathy of prematurity.Semantic proximity Read ↗

The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms.Semantic proximity Read ↗

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