Spinocerebellar Ataxia Latest Advances

Find the Latest Research About Spinocerebellar Ataxia

Last Updated: 04/28/2026

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Found 11541 publications

Home-Based Telerehabilitation for Core Stability in Hereditary Ataxia: Feasibility and Preliminary Effects of a Pilot RCT.

Home-Based Telerehabilitation for Core Stability in Hereditary Ataxia: Feasibility and Preliminary Effects of a Pilot RCT.

Journal: NeuroRehabilitation
Published: April 08, 2026

Sex specific disruptions in PKCγ signaling in a mouse model of Spinocerebellar Ataxia Type 14.

Sex specific disruptions in PKCγ signaling in a mouse model of Spinocerebellar Ataxia Type 14.

Journal: JCI insight
Published: April 02, 2026

Lentiviral-induced Striatal Pathology as a Preclinical Model of Polyglutamine Spinocerebellar Ataxias.

Lentiviral-induced Striatal Pathology as a Preclinical Model of Polyglutamine Spinocerebellar Ataxias.

Journal: Journal of visualized experiments : JoVE
Published: March 30, 2026

Identification of International Classification of Functioning, Disability and Health categories in a multifaceted rehabilitation program for degenerative cerebellar ataxia: a descriptive analysis of real-world clinical practice.

Identification of International Classification of Functioning, Disability and Health categories in a multifaceted rehabilitation program for degenerative cerebellar ataxia: a descriptive analysis of real-world clinical practice.

Journal: Disability and rehabilitation
Published: March 29, 2026

Friedreich ataxia transcriptomic dysregulation and identification of cell type-specific biomarkers: A systematic review and meta-analysis.

Friedreich ataxia transcriptomic dysregulation and identification of cell type-specific biomarkers: A systematic review and meta-analysis.

Journal: bioRxiv : the preprint server for biology
Published: March 27, 2026

Impaired motor activity in a CRISPR SCA5 L253P knock-in mouse is associated with selective β-III-spectrin subcellular redistribution in the cerebellum.

Impaired motor activity in a CRISPR SCA5 L253P knock-in mouse is associated with selective β-III-spectrin subcellular redistribution in the cerebellum.

Journal: bioRxiv : the preprint server for biology
Published: March 27, 2026

A mouse model of autosomal dominant spastic ataxia and myopathy caused by a mutation in Tuba4a.

A mouse model of autosomal dominant spastic ataxia and myopathy caused by a mutation in Tuba4a.

Journal: bioRxiv : the preprint server for biology
Published: March 27, 2026

The multifaceted nature of Friedreich ataxia: strategies for comprehensive patient care.

The multifaceted nature of Friedreich ataxia: strategies for comprehensive patient care.

Journal: Neurodegenerative disease management
Published: March 17, 2026

Identification of Biological Subtypes of Friedreich Ataxia with Structural MRI-based Machine Learning.

Identification of Biological Subtypes of Friedreich Ataxia with Structural MRI-based Machine Learning.

Journal: Radiology
Published: March 10, 2026

Spinocerebellar ataxia type 12 in a 52-year-old female.

Spinocerebellar ataxia type 12 in a 52-year-old female.

Journal: The New Zealand medical journal
Published: February 26, 2026

A case report on gait in spinocerebellar ataxia: evaluating the use of mixed reality from independent walking to integrated physical support.

A case report on gait in spinocerebellar ataxia: evaluating the use of mixed reality from independent walking to integrated physical support.

Journal: Disability and rehabilitation. Assistive technology
Published: February 26, 2026

Mutant ATXN1 impacts human and mouse microglia and contributes to cognitive, mood, and motor deficits in SCA1 mice.

Mutant ATXN1 impacts human and mouse microglia and contributes to cognitive, mood, and motor deficits in SCA1 mice.

Journal: bioRxiv : the preprint server for biology
Published: February 23, 2026
Showing 1-12 of 11,541

Last Updated: 04/28/2026