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

Central retinal preservation in rdAc cats.

Veterinary ophthalmology - 1 May 2018

Minella Andrea Louise, Occelli Laurence Mireille, Narfström Kristina, Petersen-Jones Simon Michael

Abstract excerpt

OBJECTIVE: Children with Leber congenital amaurosis (LCA) due to CEP290 mutations show characteristic macular preservation. Spectral domain-optical coherence tomography (SD-OCT) is a noninvasive technique to investigate retinal structural changes. Loss of integrity of the ellipsoid zone (EZ) on OCT in people with retinal disease has been associated with loss of visual function and is a useful measure of retinal...

Read the complete abstract on PubMed

Topics

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

Share to Cat Diseases
Share to Cats
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Optic Atrophies, Hereditary

Share to Retina

Share to Retinal Degeneration

Share to Tomography, Optical Coherence

Source

Identifiers

PMID: 28856832
DOI: 10.1111/vop.12495

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Central retinal preservation in rdAc cats.PMID 28856832Read ↗

Abnormal Appearance of the Area Centralis in Labrador Retrievers With an ABCA4 Loss-of-function Mutation.Semantic proximity Read ↗

A Comprehensive Study of the Retinal Phenotype of Rpe65-Deficient Dogs.Semantic proximity Read ↗

PRCD-associated retinitis pigmentosa in dogs and humans.Semantic proximity Read ↗

Natural history of cone disease in the murine model of Leber congenital amaurosis due to CEP290 mutation: determining the timing and expectation of therapy.Semantic proximity Read ↗

Fleck-like lesions in CEP290-associated leber congenital amaurosis: a case series.Semantic proximity Read ↗

Peripapillary sparing in RDH12-associated Leber congenital amaurosis.Semantic proximity Read ↗

Retinal Structure in RPE65-Associated Retinal Dystrophy.Semantic proximity Read ↗

Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.Semantic proximity Read ↗

Inner and outer retinal changes in retinal degenerations associated with ABCA4 mutations.Semantic proximity Read ↗

Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.Semantic proximity Read ↗

Defining inclusion criteria and endpoints for clinical trials: a prospective cross-sectional study in CRB1-associated retinal dystrophies.Semantic proximity Read ↗

Cat LCA- <i>CRX</i> model, homozygous for an antimorphic mutation has a unique phenotypeSemantic proximity Read ↗

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