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Article

Multimodal MRI in Leigh syndrome due to m.13513G > A.

Metabolic brain disease - 1 Oct 2022

Finsterer Josef

Abstract excerpt

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Topics

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DNA, Mitochondrial
Electron Transport Complex I
Leigh Disease
Magnetic Resonance Imaging
Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36018535
DOI: 10.1007/s11011-022-01072-8

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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Multimodal MRI in Leigh syndrome due to m.13513G > A.PMID 36018535Read ↗

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Striking pathology in Leigh syndrome associated with the MTATP6 T8993G mutation.Semantic proximity Read ↗

Before Leigh syndrome can be attributed to m.1608G≥A in MT-TV, its pathogenicity must be confirmed.Semantic proximity Read ↗

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Neuromitochondrial Disorders : Genomic Basis and an Algorithmic Approach to Imaging Diagnostics.Semantic proximity Read ↗

Symmetric thalamic lesions in a patient with a myoclonic epilepsy with ragged red fibers-Leigh spectrum phenotype due to the m.A8344G mutation.Semantic proximity Read ↗

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