Anna Heinzmann

Paris, France

Last Updated: 09/26/2026

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Found 26 publications

Transitional Life Events in Friedreich Ataxia: Differential Age at Onset Perspectives.

Transitional Life Events in Friedreich Ataxia: Differential Age at Onset Perspectives.

Journal: Cerebellum (London, England)

Published: March 23, 2026

A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

Journal: Cerebellum (London, England)

Published: February 08, 2026

Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease.

Sequence Variants in Small CAG Repeat Expansions of the HTT Gene and Disease Onset and Progression in Huntington Disease.

Journal: Neurology

Published: December 19, 2025

Patient-reported, psychosocial and health economic outcomes in mild to moderate Friedreich's ataxia: baseline results of the PROFA study.

Patient-reported, psychosocial and health economic outcomes in mild to moderate Friedreich's ataxia: baseline results of the PROFA study.

Journal: The Lancet regional health. Europe

Published: August 06, 2025

Spastic Ataxia Composite (SPAXCOM): A Scale to Evaluate the Progression of Subjects with Spasticity and Ataxia.

Spastic Ataxia Composite (SPAXCOM): A Scale to Evaluate the Progression of Subjects with Spasticity and Ataxia.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: April 04, 2025

Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics.

Neuropathy in GAA-FGF14 Late-Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics.

Journal: European journal of neurology

Published: March 10, 2025

The Two Faces of Pediatric SCA2.

The Two Faces of Pediatric SCA2.

Journal: European journal of neurology

Published: March 05, 2025

Hereditary spastic paraplegias: When to expect bladder dysfunction a genetic and urodynamic study.

Hereditary spastic paraplegias: When to expect bladder dysfunction a genetic and urodynamic study.

Journal: European journal of neurology

Published: October 13, 2024

SARA captures disparate progression and responsiveness in spinocerebellar ataxias.

SARA captures disparate progression and responsiveness in spinocerebellar ataxias.

Journal: Journal of neurology

Published: March 26, 2024

Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions.

Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions.

Journal: EBioMedicine

Published: October 02, 2023

CAG repeat mosaicism is gene specific in spinocerebellar ataxias.

CAG repeat mosaicism is gene specific in spinocerebellar ataxias.

Journal: American journal of human genetics

Published: September 28, 2023

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias.

Journal: American journal of human genetics

Published: March 26, 2023

Showing 1-12 of 26

Last Updated: 09/26/2026