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

Cerebellar ataxia in the eastern and southern parts of Norway.

Acta neurologica Scandinavica. Supplementum - 1 Jan 2007

Koht J, Tallaksen C M E

Abstract excerpt

INTRODUCTION: The relative frequencies of different ataxias vary among different ethnic and geographic groups. The aim of this study was to examine patients with cerebellar ataxia and find the occurrence of autosomal dominant and recessive cerebellar ataxias in the population of the southern and eastern parts of Norway and estimate its prevalence. MATERIALS AND METHODS: Probands were systematically tested for...

Read the complete abstract on PubMed

Topics

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

Share to Age Distribution
Share to Cerebellar Ataxia
Share to Chromosome Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Friedreich Ataxia

Share to Gait Disorders, Neurologic

Share to Genes, Recessive

Share to Norway

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 17419835
DOI: 10.1111/j.1600-0404.2007.00853.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cerebellar ataxia in the eastern and southern parts of Norway.PMID 17419835Read ↗

Genetic cerebellar ataxias.Semantic proximity Read ↗

Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.Semantic proximity Read ↗

[Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].Semantic proximity Read ↗

Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.Semantic proximity Read ↗

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1.Semantic proximity Read ↗

Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.Semantic proximity Read ↗

[Autosomal recessive cerebellar ataxias].Semantic proximity Read ↗

Spinocerebellar ataxia type 8 in Scotland: frequency, neurological, neuropsychological and neuropsychiatric findings.Semantic proximity Read ↗

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.Semantic proximity Read ↗

Hereditary Ataxia and Spastic Paraplegia in PortugalSemantic proximity Read ↗

SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.Semantic proximity Read ↗

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