Mathieu Anheim

11PUBLICATIONS
40CO-AUTHORS
NeurogeneticsNeurology and neuromuscular diseasesMedical biochemistry - amino acids and metabolitesSociolinguisticsGene expression (incl. microarray and other genome-wide approaches)
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Publications (11)

|Mar 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.

Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli

|Sep 22, 2025
Progress and challenges in sporadic late-onset cerebellar ataxias.

Thomas Wirth, Jennifer Faber, Christel Depienne

|Jun 02, 2025
Managing Aminotransferase Elevations in Patients with Friedreich Ataxia Treated with Omaveloxolone: A Review and Expert Opinion on Use Considerations.

Susan Perlman, Mathieu Anheim, Sylvia Boesch

|May 06, 2025
Trigeminal Tract Abnormality Leading to Leukodystrophy With Brainstem and Spinal Cord Involvement and High Lactate Diagnosis.

Irène Pei, Thomas Bogdan, Christine Tranchant

|Sep 24, 2022
The inherited cerebellar ataxias: an update.

Giulia Coarelli, Thomas Wirth, Christine Tranchant

|Jun 13, 2022
Author Response: Progression of Nigrostriatal Denervation in Cerebellar Multiple System Atrophy: A Prospective Study.

Thomas Wirth, Izzie Jacques Namer, Ben Monga

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Frequent Collaborators

6 joint publications

Thomas Wirth

3 joint publications

Christine Tranchant

2 joint publications

Caroline Bund

2 joint publications

Izzie Jacques Namer