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

Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19p

1 Jan 1997

Abstract excerpt

We describe the clinical and oculographic findings in 4 families with episodic ataxia and interictal nystagmus (EA-2) linked to chromosome 19p. Episodes varied from pure ataxia to combinations of symptoms suggesting involvement of the cerebellum, brainstem, and cortex. Some affected individuals exhibited a progressive ataxia syndrome phenotypically indistinguishable from the dominantly inherited spinocerebellar...

Read the complete abstract on PubMed

Topics

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

Share to Genetic Neurodegenerative Diseases
Share to Cerebrovascular and genetic disorders
Share to Neurological diseases and metabolism

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

Source

Identifiers

PMID: 9005860
DOI: 10.1002/ana.410410105

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

Familial episodic ataxia: Clinical heterogeneity in four families linked to chromosome 19pPMID 9005860Read ↗

Episodic vertical oscillopsia with progressive gait ataxia: clinical description of a new episodic syndrome and evidence of linkage to chromosome 13q.Semantic proximity Read ↗

A new episodic ataxia syndrome with linkage to chromosome 19q13.Semantic proximity Read ↗

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.Semantic proximity Read ↗

Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood.Semantic proximity Read ↗

Clinical spectrum of episodic ataxia type 2.Semantic proximity Read ↗

Phenotypic variability of episodic ataxia type 2 mutations: a family study.Semantic proximity Read ↗

Spinocerebellar Ataxia 27 A with Episodic Ataxia: Case Series of Fibroblast Growth Factor 14 (FGF14) Microdeletions.Semantic proximity Read ↗

Episodic ataxia type 2 characterised by recurrent dizziness/vertigo: a report of four cases.Semantic proximity Read ↗

Episodic Ataxias: Faux or Real?Semantic proximity Read ↗

Familial episodic ataxia: a model for migrainous vertigo.Semantic proximity Read ↗

FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9.Semantic proximity Read ↗

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?Semantic proximity Read ↗

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