Spinocerebellar Ataxia Type 5 Latest Advances

Find the Latest Research About Spinocerebellar Ataxia Type 5

Last Updated: 09/26/2026

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Found 3608 publications

Nongenetic Factors Associated With Onset and Severity of Hereditary Ataxia.

Nongenetic Factors Associated With Onset and Severity of Hereditary Ataxia.

Journal: Neurology
Published: August 05, 2026

Cervical dystonia as the presenting symptom of novel calcium voltage-gated channel subunit alpha1A mutation.

Cervical dystonia as the presenting symptom of novel calcium voltage-gated channel subunit alpha1A mutation.

Journal: BMJ case reports
Published: August 03, 2026

Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats.

Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats.

Journal: RNA biology
Published: June 24, 2026

From genes to neuropathology: Integrative perspectives on the spectrum of spinocerebellar ataxias.

From genes to neuropathology: Integrative perspectives on the spectrum of spinocerebellar ataxias.

Journal: Clinical neuropathology
Published: June 15, 2026

Downbeat nystagmus without ataxia as an early manifestation of spinocerebellar ataxia, autosomal recessive type 10 (SCAR10): a case report.

Downbeat nystagmus without ataxia as an early manifestation of spinocerebellar ataxia, autosomal recessive type 10 (SCAR10): a case report.

Journal: Neurogenetics
Published: May 30, 2026

Aromatic-Turmerone Analogs Activate Chaperone-Mediated Autophagy and Ameliorate Dendritic Shrinkage in Purkinje Cell Models of Spinocerebellar Ataxia.

Aromatic-Turmerone Analogs Activate Chaperone-Mediated Autophagy and Ameliorate Dendritic Shrinkage in Purkinje Cell Models of Spinocerebellar Ataxia.

Journal: Biological & pharmaceutical bulletin
Published: May 27, 2026

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

Journal: Human molecular genetics
Published: May 22, 2026

The recurrent SACS gene p.Arg272His hotspot expands the neurodevelopmental and cognitive spectrum of ARSACS.

The recurrent SACS gene p.Arg272His hotspot expands the neurodevelopmental and cognitive spectrum of ARSACS.

Journal: Neurogenetics
Published: May 15, 2026

Nuclear Lamina Dysfunction and DNA Damage as Drivers of Premature Senescence in a Human Müller Glial Cell Model of Spinocerebellar Ataxia Type 7.

Nuclear Lamina Dysfunction and DNA Damage as Drivers of Premature Senescence in a Human Müller Glial Cell Model of Spinocerebellar Ataxia Type 7.

Journal: International journal of molecular sciences
Published: May 12, 2026

Management of spinocerebellar ataxia.

Management of spinocerebellar ataxia.

Journal: Neurodegenerative disease management
Published: April 30, 2026

Genotypic features of Spinocerebellar Ataxia in Northern China: A Comparative Analysis with Southern China.

Genotypic features of Spinocerebellar Ataxia in Northern China: A Comparative Analysis with Southern China.

Journal: Cerebellum (London, England)
Published: April 28, 2026

Cerebellar Cognitive Affective Syndrome in Spinocerebellar Ataxia Type 6.

Cerebellar Cognitive Affective Syndrome in Spinocerebellar Ataxia Type 6.

Journal: Cerebellum (London, England)
Published: April 26, 2026
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Last Updated: 09/26/2026