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

Cerebellar Stroke-Like Lesion in an m.13513G>A Carrier with Leigh Syndrome.

Neurology India - 1 Jan 2000

Finsterer Josef

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 Leigh Disease
Share to Mutation
Share to Stroke

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 37148092
DOI: 10.4103/0028-3886.375416

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cerebellar Stroke-Like Lesion in an m.13513G>A Carrier with Leigh Syndrome.PMID 37148092Read ↗

Multimodal MRI in Leigh syndrome due to m.13513G > A.Semantic proximity Read ↗

Adult-Onset Leigh Syndrome Due to an m.13513G>A Mutation.Semantic proximity Read ↗

Rostral brain lesions of Leigh syndrome associated with the mitochondrial DNA 8993T>G mutation.Semantic proximity Read ↗

Cerebellar hematoma in a carrier of the A3243G MELAS mutation.Semantic proximity Read ↗

Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.Semantic proximity Read ↗

Molecular basis of Leigh syndrome: a current look.Semantic proximity Read ↗

Walking difficulties and brainstem dysfunction: a case report of adult onset Leigh syndromeSemantic proximity Read ↗

Homoplasmy of the m. 8993 T>G variant in a patient without MRI findings of Leigh syndrome, ataxia or retinal abnormalities.Semantic proximity Read ↗

Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review.Semantic proximity Read ↗

A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes.Semantic proximity Read ↗

Mitochondrial DNA Mutations Linking Leigh Syndrome and Carotid Atherosclerosis: A Study of Shared Genetic PathwaysSemantic proximity Read ↗

SCL19A3 gene mutation with Leigh-like phenotype presentation: a potentially treatable disease.Semantic proximity Read ↗

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