Acute periaqueductal syndrome associated with the G11778A mitochondrial DNA mutation.

doi:10.1212/wnl.56.4.570

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

Community

Back to search

Article

Acute periaqueductal syndrome associated with the G11778A mitochondrial DNA mutation.

Neurology - 27 Feb 2001

Riggs J E, Ellis B D, Hogg J P, Al-Azzaz A, Schochet S S

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 DNA, Mitochondrial
Share to Magnetic Resonance Imaging
Share to Mutation
Share to Neurodegenerative Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Optic Atrophies, Hereditary

Share to Syndrome

Source

Open in PubMed

Identifiers

PMID: 11222813
DOI: 10.1212/wnl.56.4.570

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Acute periaqueductal syndrome associated with the G11778A mitochondrial DNA mutation.PMID 11222813Read ↗

Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?Semantic proximity Read ↗

Variable clinical expression associated with the mutation 3243 np of mitochondrial DNA.Semantic proximity Read ↗

Chronic diarrhea associated with the A3243G mtDNA mutation.Semantic proximity Read ↗

Neurologic disorders due to mitochondrial DNA mutations.Semantic proximity Read ↗

Neurological diseases due to mitochondrial DNA mutations: concepts and problems in pathogenesis.Semantic proximity Read ↗

Mitochondrial DNA: impacting central and peripheral nervous systems.Semantic proximity Read ↗

The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.Semantic proximity Read ↗

Physiology and pathophysiology of mitochondrial DNA.Semantic proximity Read ↗

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