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Article

MELAS syndrome: a mitochondrially inherited disorder.

International ophthalmology clinics - 1 Jan 1993

Stroh E M, Winterkorn J M, Jalkh A E, Lessell S

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Identifiers

PMID: 8325731
DOI: 10.1097/00004397-199303320-00016

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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→

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MELAS syndrome: a mitochondrially inherited disorder.PMID 8325731Read ↗

Clinical and biochemical phenotype of the MELAS mutation.Semantic proximity Read ↗

MELAS syndrome.Semantic proximity Read ↗

Mutations of the mitochondrial ND1 gene as a cause of MELAS.Semantic proximity Read ↗

A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation.Semantic proximity Read ↗

Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).Semantic proximity Read ↗

[MERRF/MELAS overlap syndrome].Semantic proximity Read ↗

[MERRF/MELAS overlap syndrome].Semantic proximity Read ↗

MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesisSemantic proximity Read ↗

Cardiac Involvement in Adults With m.3243A>G MELAS Gene MutationSemantic proximity Read ↗

A whole mitochondrial genome screening in a MELAS patient: a novel mitochondrial tRNA(Val) mutation.Semantic proximity Read ↗

Clinical spectrum of the MELAS mutation in a large pedigree.Semantic proximity Read ↗

MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.Semantic proximity Read ↗

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