Thomas Wirth

24PUBLICATIONS

92CO-AUTHORS

Gene and molecular therapyNeurogeneticsNeurology and neuromuscular diseasesSociolinguisticsGenomics

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Publications (24)

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|Jun 12, 2026

Bispecific antibody therapy in multiple myeloma and risk of progressive multifocal leukoencephalopathy.

|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 28, 2025

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

Julian Theuriet, Lukas Paulet, Blandine Acket

|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

|Apr 23, 2025

Long-Read Sequencing: The Third Generation of Diagnostic Testing for Dystonia.

Thomas Wirth, Kishore R Kumar, Michael Zech

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Frequent Collaborators

Mathieu Anheim

Aurélie Méneret

Christine Tranchant

Gabrielle Rudolf

Caroline Bund

Laura Cif

Izzie Jacques Namer

Jean-Pierre Lin

Manju A Kurian

Christine Y Kim

Frequent Collaborators

Mathieu Anheim

Aurélie Méneret

Christine Tranchant

Gabrielle Rudolf