Jean-baptiste B. Chanson

Strasbourg, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 65 publications

Does CANVAS mimic MSA-C? A prospective multimodal study.

Does CANVAS mimic MSA-C? A prospective multimodal study.

Journal: Journal of neurology

Published: May 29, 2026

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Journal: Neurology

Published: January 15, 2026

Enhanced proteasome activity in perifascicular myofibres is a hallmark of dermatomyositis and its inhibition is efficient in preclinical models.

Enhanced proteasome activity in perifascicular myofibres is a hallmark of dermatomyositis and its inhibition is efficient in preclinical models.

Journal: Annals of the rheumatic diseases

Published: April 30, 2025

Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry.

Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registry.

Journal: Orphanet journal of rare diseases

Published: April 09, 2025

Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy.

Nationwide Phenotypic and Genotypic Characterisation of 103 Patients With SH3TC2 Gene-Related Demyelinating Peripheral Neuropathy.

Journal: European journal of neurology

Published: April 08, 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

Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort study.

Phenotype-genotype correlation in X-linked Charcot-Marie-Tooth disease: A French cohort study.

Journal: European journal of neurology

Published: May 03, 2024

Clinical and Electrophysiological Characteristics of 23 French Patients With Neurolymphomatosis.

Clinical and Electrophysiological Characteristics of 23 French Patients With Neurolymphomatosis.

Journal: Muscle & nerve

Published: March 28, 2024

Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study.

Diagnosis of hereditary transthyretin amyloidosis in patients with suspected chronic inflammatory demyelinating polyneuropathy unresponsive to intravenous immunoglobulins: results of a retrospective study.

Journal: Orphanet journal of rare diseases

Published: March 25, 2024

Identification of rare variants in the FBXO38 gene of patients with chronic inflammatory demyelinating polyradiculoneuropathy.

Identification of rare variants in the FBXO38 gene of patients with chronic inflammatory demyelinating polyradiculoneuropathy.

Journal: Journal of neuroimmunology

Published: February 28, 2024

Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndrome.

Clinical, paraclinical and outcome features of 166 patients with acute anti-GQ1b antibody syndrome.

Journal: Journal of neurology

Published: January 31, 2024

Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?

Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?

Journal: Journal of neurology

Published: December 20, 2023

Showing 1-12 of 65

Last Updated: 09/26/2026