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

Retinal Imaging Findings in Inherited Retinal Diseases

3 Apr 2024

Abstract excerpt

Inherited retinal diseases (IRDs) represent one of the major causes of progressive and irreversible vision loss in the working-age population. Over the last few decades, advances in retinal imaging have allowed for an improvement in the phenotypic characterization of this group of diseases and have facilitated phenotype-to-genotype correlation studies. As a result, the number of clinical trials targeting IRDs has...

Read the complete abstract on PubMed

Topics

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

Share to Ocular Disorders and Treatments
Share to Retinal Development and Disorders
Share to Retinal Diseases and Treatments

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

Source

Identifiers

PMID: 38610844
DOI: 10.3390/jcm13072079

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 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

Retinal Imaging Findings in Inherited Retinal DiseasesPMID 38610844Read ↗

Imaging in inherited retinal disorders.Semantic proximity Read ↗

Retinitis pigmentosa: recent advances and future directions in diagnosis and managementSemantic proximity Read ↗

Inherited retinal diseases: Therapeutics, clinical trials and end points—A reviewSemantic proximity Read ↗

Inherited retinal degenerations: clinical phenotypes and emerging therapies.Semantic proximity Read ↗

Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes.Semantic proximity Read ↗

Macular dystrophies: clinical and imaging features, molecular genetics and therapeutic optionsSemantic proximity Read ↗

Inherited Retinal Degenerations: Current Landscape and Knowledge GapsSemantic proximity Read ↗

The molecular basis of human retinal and vitreoretinal diseases.Semantic proximity Read ↗

Inherited and orphan retinal diseases: phenotypes, genotypes, and probable treatment groups.Semantic proximity Read ↗

Revisiting Retinal Degeneration Hallmarks: Insights from Molecular Markers and Therapy PerspectivesSemantic proximity Read ↗

Genetic testing and diagnosis of inherited retinal diseases.Semantic proximity Read ↗

Approach to inherited retinal diseases.Semantic proximity Read ↗

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