Guillaume Nicolas

Montigny-sur-loing, 78180, France

Last Updated: 09/26/2026

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Found 68 publications

High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.

High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: July 31, 2026

A qualitative study of the discrepancy between patient expectations and assessment practices in 5q-adult spinal muscular atrophy in France.

A qualitative study of the discrepancy between patient expectations and assessment practices in 5q-adult spinal muscular atrophy in France.

Journal: Journal of neuromuscular diseases

Published: April 24, 2026

Long-term treatment outcomes of immune checkpoint inhibitor-related neuropathies: a French multicenter cohort study.

Long-term treatment outcomes of immune checkpoint inhibitor-related neuropathies: a French multicenter cohort study.

Journal: Scientific reports

Published: February 25, 2026

Feasibility and usefulness of personalised patient-reported outcome measures in the therapeutic follow-up of adult spinal muscular atrophy patients.

Feasibility and usefulness of personalised patient-reported outcome measures in the therapeutic follow-up of adult spinal muscular atrophy patients.

Journal: Clinical neurology and neurosurgery

Published: February 22, 2026

Acute inflammatory polyradiculoneuritis (Guillain-Barré syndrome)

Acute inflammatory polyradiculoneuritis (Guillain-Barré syndrome)

Journal: La Revue du praticien

Published: January 23, 2026

Whole-Body Muscle MRI in Non-5q Spinal Muscular Atrophy: Patterns, Genotype Prediction, and Diagnostic Implications.

Whole-Body Muscle MRI in Non-5q Spinal Muscular Atrophy: Patterns, Genotype Prediction, and Diagnostic Implications.

Journal: Neurology. Genetics

Published: December 16, 2025

Electrophysiological assessment of motor unit loss in adult spinal muscular atrophy types III and IV: a multicenter national study comparing MUNIX, CMAP, and MUSIX.

Electrophysiological assessment of motor unit loss in adult spinal muscular atrophy types III and IV: a multicenter national study comparing MUNIX, CMAP, and MUSIX.

Journal: Journal of neurology

Published: November 19, 2025

Presymptomatic late-onset Pompe disease: Optimizing the timing of treatment.

Presymptomatic late-onset Pompe disease: Optimizing the timing of treatment.

Journal: Revue neurologique

Published: June 27, 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

Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure.

Homozygous DNAJB4 deletion revealing myopathy with acute respiratory failure.

Journal: Revue neurologique

Published: March 11, 2025

Are Dry-Land Force-Velocity Abilities Related to In-Water Load-Velocity Profiles in Sprint Swimming?

Are Dry-Land Force-Velocity Abilities Related to In-Water Load-Velocity Profiles in Sprint Swimming?

Journal: European journal of sport science

Published: September 17, 2024

Autosomal dominant distal myopathy due to p.Ser85Cys mutation in the MATR3 gene: Novel case series and literature review.

Autosomal dominant distal myopathy due to p.Ser85Cys mutation in the MATR3 gene: Novel case series and literature review.

Journal: Revue neurologique

Published: July 19, 2024

Showing 1-12 of 68

Last Updated: 09/26/2026