Hereditary Ataxia Latest Advances

Pharmacotherapy of neuromuscular diseases : what's new in 2025

Journal: Revue medicale suisse

Published: January 16, 2026

Enhancing the Objective Assessment of Friedreich Ataxia Severity: A Multiview IMU-Based Approach.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 03, 2025

Reliable Objective Assessment of Friedreich Ataxia Through Isolation Forest-Based Anomaly Detection.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 03, 2025

Objective Assessment of Friedreich Ataxia in Children: Accounting for Developmental Deficits.

Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference

Published: December 03, 2025

A case of Friedreich Ataxia and left ventricular hypertrophy induced by FXN gene mutation

Journal: Zhonghua xin xue guan bing za zhi

Published: November 25, 2025

Purkinje cell development and degeneration in the spastic Han-Wistar rat model of ataxia.

Journal: Research square

Published: November 24, 2025

Type 28 spinocerebellar ataxia

Journal: Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova

Published: November 20, 2025

Genetic testing for adult-onset neurodegenerative diseases: A clinical perspective.

Journal: Journal of the Formosan Medical Association = Taiwan yi zhi

Published: October 29, 2025

Polyphenol-Enriched Fraction from Chestnut Shells as a Source of Bioactive Compounds for Friedreich Ataxia.

Journal: Molecules (Basel, Switzerland)

Published: October 28, 2025

Purkinje cell development and degeneration in the spastic Han-Wistar rat model of ataxia.

Journal: bioRxiv : the preprint server for biology

Published: October 03, 2025

A Novel SIL1 Variant (p.E342K) Associated with Marinesco-Sjögren Syndrome Impairs Protein Stability and Function.

Journal: International journal of molecular sciences

Published: October 01, 2025

Identification of a Novel CLPX Variant in a Mixed-Breed Dog with Anemia and Spinocerebellar Ataxia.

Journal: Genes

Published: September 20, 2025