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

Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13(R420H).

Neurology - 11 Sept 2012

Waters Michael F, Subramony Sankarasubramoney H, Advincula Joel, Perlman Susan, Ashizawa Tetsuo

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 Aged
Share to Aged, 80 and over
Share to Child
Share to Eye Movements

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Spinocerebellar Ataxias

Share to Spinocerebellar Degenerations

Source

Open in PubMed Open full text

Identifiers

PMID: 22933745
DOI: 10.1212/WNL.0b013e3182698d5c
PMCID: PMC3525304

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

Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13(R420H).PMID 22933745Read ↗

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

Ocular Motor and Vestibular Profile in Spinocerebellar Ataxia Type 27B: Toward a Practical Bedside Diagnostic FrameworkSemantic proximity Read ↗

Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes.Semantic proximity Read ↗

Oculomotor phenotypes in autosomal dominant ataxias.Semantic proximity Read ↗

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

Executive functions are impaired in heterozygote patients with oculopharyngeal muscular dystrophySemantic proximity Read ↗

The Association Between Diplopia and Clinical Phenotypes in Spinocerebellar Ataxia Type 3Semantic proximity Read ↗

Oculomotor Abnormalities and Nystagmus in Brainstem Disease: A Mini ReviewSemantic proximity Read ↗

Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression.Semantic proximity Read ↗

Patient-reported Vision Quality-of-life in Parkinsonian Syndromes and Ataxias and Association with Clinical Oculomotor FindingsSemantic proximity Read ↗

Abnormal Vertical Eye Movements as a Clue for Diagnosis of Niemann-Pick Type C.Semantic proximity Read ↗

Pitfalls in ataxia with ocular motor apraxia type 1: pseudodominant inheritance and very late onset.Semantic proximity Read ↗

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