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Article

Electroretinogram in Duchenne/Becker muscular dystrophy.

Pediatric neurology - 1 Apr 1998

Pascual Pascual S I, Molano J, Pascual-Castroviejo I

Abstract excerpt

The authors studied all cases with dystrophinopathy consecutively reviewed between May 1995 and December 1996 by means of electroretinography (ERG), which was recorded using skin eyelid electrodes and with standard flash stimulation. This methodology can detect the functional abnormalities associated with dystrophinopathies. The most valuable parameter is the ratio of B-wave amplitude to A-wave amplitude (B/A...

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Source

Identifiers

PMID: 9588526
DOI: 10.1016/s0887-8994(97)00208-7

Genes

DMD
ERG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 9 closest

Electroretinogram in Duchenne/Becker muscular dystrophy.PMID 9588526Read ↗

[Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy].Semantic proximity Read ↗

Electroretinogram abnormalities in FKRP-related limb-girdle muscular dystrophy (LGMDR9).Semantic proximity Read ↗

Electroretinographic findings in Duchenne/Becker muscular dystrophy and correlation with genotype.Semantic proximity Read ↗

Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.Semantic proximity Read ↗

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.Semantic proximity Read ↗

Multifocal electroretinogram contributes to differentiation of various clinical pictures within a family with Bardet-Biedl syndrome.Semantic proximity Read ↗

The electroretinographic phenotype of dogs with Golden Retriever muscular dystrophy.Semantic proximity Read ↗

Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations.Semantic proximity Read ↗

ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy.Semantic proximity Read ↗

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