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 phenotypes in autosomal dominant ataxias.

Archives of neurology - 1 Oct 1998

Buttner N, Geschwind D, Jen J C, Perlman S, Pulst S M, Baloh R W

Abstract excerpt

OBJECTIVE: To quantify the oculomotor features of the common spinocerebellar ataxia (SCA) syndromes. SETTING: University ataxia clinic. PATIENTS: Twenty probands with documented SCA mutations. METHODS: Electro-oculographic recordings of saccadic, smooth pursuit, optokinetic, vestibular, and visual-vestibular eye movements. RESULTS: Distinct phenotype and genotype patterns were identified with modest overlap...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Chromosome Aberrations
Share to Chromosome Disorders

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genotype

Share to Phenotype

Share to Retinal Degeneration

Share to Spinocerebellar Degenerations

Source

Identifiers

PMID: 9779665
DOI: 10.1001/archneur.55.10.1353

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Oculomotor phenotypes in autosomal dominant ataxias.PMID 9779665Read ↗

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

Slow saccades and other eye movement disorders in spinocerebellar atrophy type 1.Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.Semantic proximity Read ↗

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

Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I.Semantic proximity Read ↗

The spinocerebellar ataxias.Semantic proximity Read ↗

Ocular motility in genetically defined autosomal dominant cerebellar ataxia.Semantic proximity Read ↗

Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).Semantic proximity Read ↗

[Study of oculomotor disorders in spinocerebellar ataxia genotype].Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?Semantic proximity Read ↗

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