Olivopontocerebellar Atrophy Latest Advances

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.

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.

Journal: Disability and rehabilitation

Published: March 29, 2026

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

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.

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.

Journal: bioRxiv : the preprint server for biology

Published: February 23, 2026

Retrotransposition Events Shape the Evolution of the Ataxin-3 Gene Family in Primates.

Journal: Genome biology and evolution

Published: February 20, 2026

Clinicopathologic Correlates: Progressive Downbeat Nystagmus in Spinocerebellar Ataxia Type 27B.

Journal: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society

Published: February 17, 2026

Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later Adulthood.

Journal: Neurology

Published: February 16, 2026

Genetic analyses enabled by the Fourth Chromosome Resource Projectreveal unexpected mutant phenotypes and suggest new disease models.

Journal: G3 (Bethesda, Md.)

Published: February 15, 2026

Patient-reported Vision Quality-of-life in Parkinsonian Syndromes and Ataxias and Association with Clinical Oculomotor Findings.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Olivopontocerebellar Atrophy Latest Advances

Find the Latest Research About Olivopontocerebellar Atrophy

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.

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

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

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.

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.

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

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

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.

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.

Retrotransposition Events Shape the Evolution of the Ataxin-3 Gene Family in Primates.

Retrotransposition Events Shape the Evolution of the Ataxin-3 Gene Family in Primates.

Clinicopathologic Correlates: Progressive Downbeat Nystagmus in Spinocerebellar Ataxia Type 27B.

Clinicopathologic Correlates: Progressive Downbeat Nystagmus in Spinocerebellar Ataxia Type 27B.

Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later Adulthood.

Pearls & Oy-sters: SCA27B as an Elusive Genetic Cause of Episodic Neurologic Symptoms in Later Adulthood.

Genetic analyses enabled by the Fourth Chromosome Resource Projectreveal unexpected mutant phenotypes and suggest new disease models.

Genetic analyses enabled by the Fourth Chromosome Resource Projectreveal unexpected mutant phenotypes and suggest new disease models.

Patient-reported Vision Quality-of-life in Parkinsonian Syndromes and Ataxias and Association with Clinical Oculomotor Findings.

Patient-reported Vision Quality-of-life in Parkinsonian Syndromes and Ataxias and Association with Clinical Oculomotor Findings.