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Last Updated: 03/06/2025
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Found 195 publications
ATXN10 Gene Expansions in Mexican Patients with Ataxia Without Epilepsy.
Journal: Cerebellum (London, England)
Published: December 31, 2024
Polyneuropathy in Patients with Spinocerebellar Ataxias Types 2, 3, and 10: A Systematic Review.
Journal: Cerebellum (London, England)
Published: August 06, 2024
Spatiotemporal Gait Analysis of Patients with Spinocerebellar Ataxia Types 3 and 10 Using Inertial Measurement Units: A Comparative Study.
Journal: Cerebellum (London, England)
Published: June 03, 2024
Extended haplotype with rs41524547-G defines the ancestral origin of SCA10.
Journal: Human molecular genetics
Published: November 21, 2023
Spinocerebellar ataxia type 10 and Huntington disease-like 2 in Venezuela: Further evidence of two different ancestral founder effects.
Journal: Annals of human genetics
Published: July 13, 2023
Structures and conformational dynamics of DNA minidumbbells in pyrimidine-rich repeats associated with neurodegenerative diseases.
Journal: Computational and structural biotechnology journal
Published: September 26, 2022
Mechanistic and Therapeutic Insights into Ataxic Disorders with Pentanucleotide Expansions.
Journal: Cells
Published: April 14, 2022
Spinocerebellar Ataxia Type 10 with Atypical Clinical Manifestation in Han Chinese.
Journal: Cerebellum (London, England)
Published: April 06, 2022
Widening the spectrum of spinocerebellar ataxia autosomal recessive type 10 (SCAR10).
Journal: BMJ case reports
Published: March 08, 2022
Last Updated: 03/06/2025