Overview
Spinocerebellar disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Research Evidence
Peer-reviewed studies linked via MeSH term "Spinocerebellar Degenerations" from the MEDLINE/PubMed database.
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Best Oculomotor Endpoints for Clinical Trials in Hereditary Ataxias: A Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital‑Motor Biomarkers.
[object Object], [object Object], [object Object] et al. · Cerebellum · 2025
A systematic review of social cognition in hereditary ataxia patients: Evidence from neuroimaging studies.
[object Object], [object Object], [object Object] et al. · Brain Res · 2024
PMID: 38219813Meta-Analysis
Gene Suppression Therapies in Hereditary Cerebellar Ataxias: A Systematic Review of Animal Studies.
[object Object], [object Object], [object Object] et al. · Cells · 2023
Association between restless legs syndrome and other movement disorders.
[object Object], [object Object], [object Object] et al. · Neurology · 2019
PMID: 31004074Meta-Analysis
Treatment for dysphagia (swallowing difficulties) in hereditary ataxia.
[object Object], [object Object], [object Object] et al. · Cochrane Database Syst Rev · 2015
The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
[object Object], [object Object], [object Object] et al. · Neuroepidemiology · 2014
PMID: 24603320Meta-Analysis
Treatment for speech disorder in Friedreich ataxia and other hereditary ataxia syndromes.
[object Object], [object Object], [object Object] · Cochrane Database Syst Rev · 2014
Effectiveness and safety of treatments for degenerative ataxias: a systematic review.
[object Object], [object Object], [object Object] et al. · Mov Disord · 2009
PMID: 19412936Meta-Analysis
Goal-Directed Rehabilitation Versus Standard Care for Individuals with Hereditary Cerebellar Ataxia: A Multicenter, Single-Blind, Randomized Controlled Superiority Trial.
[object Object], [object Object], [object Object] et al. · Ann Neurol · 2025
PMID: 39520242RCT
Effectiveness of functional trunk training on trunk control and upper limb functions in patients with autosomal recessive hereditary ataxia.
[object Object], [object Object], [object Object] et al. · NeuroRehabilitation · 2022
PMID: 35311719RCT
Search all PubMed articles for Spinocerebellar disease
Research data from MEDLINE/PubMed
Related Conditions
Friedreich's ataxia(child)
Corticostriatal-spinal degeneration(child)
Jervis' syndrome(child)
Athetosis with spastic paraplegia(child)
Bailey-Cushing syndrome(child)
Paramyoclonus multiplex(child)
Ataxia-telangiectasia syndrome(child)
Posthemiplegic ataxia(child)
Progressive spinocerebellar ataxia with retained tendon reflexes(child)
Vestibulocerebellar ataxia(child)
Nothnagel's syndrome(child)
Sanger-Brown cerebellar ataxia(child)
Spinocerebellar ataxia(child)
MEMSA - myoclonic epilepsy myopathy sensory ataxia(child)
Spinocerebellar degeneration co-occurrent with macular corneal dystrophy(child)
COASY gene related pontocerebellar hypoplasia(child)
Cerebellar disorder(parent)
Encephalomyelopathy(parent)
Quick Facts
- SNOMED CT
- 91502009
- UMLS CUI
- C0037952
- Fully Specified Name
- Spinocerebellar disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.