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

Dominant optic atrophy, neuropathy, ataxia, white matter FLAIR hypersignals, middle cerebellar peduncule atrophy and asthenia in OPA1 mutation.

European neurology - 1 Jan 2012

Magnin Eloi, Allibert Remi, Berger Eric, Dollfus Helene, Rumbach Lucien

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 Cerebellar Ataxia
Share to Fluorescein Angiography
Share to OPA1 gene
Share to GTP Phosphohydrolases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Leukoencephalopathies

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Optic Atrophy, Autosomal Dominant

Source

Identifiers

PMID: 22472598
DOI: 10.1159/000336743

Genes

OPA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dominant optic atrophy, neuropathy, ataxia, white matter FLAIR hypersignals, middle cerebellar peduncule atrophy and asthenia in OPA1 mutation.PMID 22472598Read ↗

Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy.Semantic proximity Read ↗

OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets.Semantic proximity Read ↗

Subclinical multisystem neurologic disease in "pure" OPA1 autosomal dominant optic atrophy.Semantic proximity Read ↗

Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates.Semantic proximity Read ↗

[Not only optic neuropathy: new molecular and clinical aspects of OPA1 gene mutations].Semantic proximity Read ↗

Multi-system neurological disease is common in patients with OPA1 mutations.Semantic proximity Read ↗

OPA1: How much do we know to approach therapy?Semantic proximity Read ↗

Similar oculomotor phenotypes in episodic ataxia type 2 and spinocerebellar atrophy type 6.Semantic proximity Read ↗

Heterozygous type 1 Autosomal Dominant Optic Atrophy (ADOA) with OPA1 c.1936-2A>G genetic variant.Semantic proximity Read ↗

Dominant optic atrophySemantic proximity Read ↗

Dominant optic atrophy: updates on the pathophysiology and clinical manifestations of the optic atrophy 1 mutation.Semantic proximity Read ↗

Comparisons of clinical phenotype, radiological and laboratory features, and therapy of neuromyelitis optica spectrum disorder by regions: update and challenges.Semantic proximity Read ↗

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