Spinocerebellar Ataxia Type 31 Latest Advances
Find the Latest Research About Spinocerebellar Ataxia Type 31
Last Updated: 04/28/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 83 publications
Long-term efficacy and disease-specific responsiveness to protirelin in patients with spinocerebellar degeneration: A retrospective study.
Journal: Parkinsonism & related disorders
Published: December 21, 2025
Characteristics of dysarthria in patients with spinocerebellar degeneration and multiple system atrophy: a cross-sectional and longitudinal study using the Frenchay Dysarthria Assessment Second Edition (FDA-2).
Journal: Frontiers in neurology
Published: October 28, 2025
Phototriggered Morphological and Compositional Change of UGGAA Repeat RNA Foci by Photoswitchable RNA-Binding Ligand.
Journal: Angewandte Chemie (International ed. in English)
Published: October 09, 2025
Spino-cerebellar Ataxia 31 presenting as a demyelinating disease: a case report.
Journal: Acta neurologica Belgica
Published: July 11, 2025
Long-Term Effects of Annual Intensive Rehabilitation in Patients with Hereditary Pure Cerebellar Ataxia: A 7-year Follow-up Study.
Journal: Cerebellum (London, England)
Published: May 09, 2025
Naphthyridine carbamate dimer ligand induces formation of Z-RNA-like fold of disease-related RNA and exhibits a molecular glue characteristics in crystal lattice formation.
Journal: Nucleic acids research
Published: April 17, 2025
[18F]THK5351 uptake in multiple system atrophy compared with other parkinsonian disorders.
Journal: Journal of neurology
Published: March 14, 2025
A Review of Spinocerebellar Ataxias in Taiwan.
Journal: Acta neurologica Taiwanica
Published: August 26, 2024
Prevalence of repeat expansions causing autosomal dominant spinocerebellar ataxias in Hokkaido, the northernmost island of Japan.
Journal: Journal of human genetics
Published: July 14, 2023
Last Updated: 04/28/2026