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

Ocular phenotype and electroretinogram abnormalities in Lafora disease: A "window to the brain".

Neurology - 17 Jul 2018

Vincent Ajoy, Macrì Angelo, Tumber Anupreet, Koukas Nikolas, Ahonen Saija, Striano Pasquale, Minassian Berge

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Brain
Share to Carrier Proteins
Share to Electroretinography
Share to Eye

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lafora Disease

Share to Phenotype

Share to Ubiquitin-Protein Ligases

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 29907606
DOI: 10.1212/WNL.0000000000005821
PMCID: PMC6059029

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ocular phenotype and electroretinogram abnormalities in Lafora disease: A "window to the brain".PMID 29907606Read ↗

Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stage.Semantic proximity Read ↗

Molecular Biology of the Eye: Genes, Vision, and Ocular DiseaseSemantic proximity Read ↗

Molecular Biology of the Eye: Genes, Vision, and Ocular DiseaseSemantic proximity Read ↗

The electroretinogram in the genomics era: outer retinal disorders.Semantic proximity Read ↗

[Inherited ophthalmological disorders. Part 1: Genetic fundamentals and phenotypes].Semantic proximity Read ↗

[Inherited ophthalmological disorders. Part 2: Diagnostics and therapeutic concepts].Semantic proximity Read ↗

Down syndrome and the eye: Ocular characteristics and ocular assessmentSemantic proximity Read ↗

Aniridia: a comparative overview.Semantic proximity Read ↗

Nonepileptic visual hallucinations in Lafora disease.Semantic proximity Read ↗

OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets.Semantic proximity Read ↗

A case of Axenfeld-Rieger syndrome (ARS) with asymmetric ocular phenotypes and left glaucomatous optic atrophy.Semantic proximity Read ↗

Genetic diseases of the eye. Edited By elias I. Traboulsi. New york and oxford: oxford university press, 1998. Pp. 876. $198.50Semantic proximity Read ↗

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