Hereditary Ataxia Latest Advances

Find the Latest Research About Hereditary Ataxia

Last Updated: 04/28/2026

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Found 5450 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

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

Clinical and genetic diagnostic challenges in presumed hereditary ataxia.

Clinical and genetic diagnostic challenges in presumed hereditary ataxia.

Journal: Journal of neurology
Published: January 28, 2026

Pharmacotherapy of neuromuscular diseases : what's new in 2025

Pharmacotherapy of neuromuscular diseases : what's new in 2025

Journal: Revue medicale suisse
Published: January 16, 2026

CGG Repeat Expansion in GIPC1 is Associated with Childhood-Onset Hereditary Ataxia.

CGG Repeat Expansion in GIPC1 is Associated with Childhood-Onset Hereditary Ataxia.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 16, 2026

Long-term efficacy and disease-specific responsiveness to protirelin in patients with spinocerebellar degeneration: A retrospective study.

Long-term efficacy and disease-specific responsiveness to protirelin in patients with spinocerebellar degeneration: A retrospective study.

Journal: Parkinsonism & related disorders
Published: December 21, 2025

Longitudinal analysis shows GAA1 length and baseline clinical status as robust predictors of progression in Friedreich ataxia.

Longitudinal analysis shows GAA1 length and baseline clinical status as robust predictors of progression in Friedreich ataxia.

Journal: Journal of neurology
Published: December 17, 2025

Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review.

Biallelic Truncating DNAH14 Variant in Siblings with Neurodevelopmental Disorder and Predominant Ataxia: Clinical Report and Literature Review.

Journal: International journal of molecular sciences
Published: December 09, 2025

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

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.

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.

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

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
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Last Updated: 04/28/2026