Emmanuelle Campana-Salort

Central Parkway
Newcastle Upon Tyne, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 125 publications

Biomarkers in facioscapulohumeral muscular dystrophy.

Biomarkers in facioscapulohumeral muscular dystrophy.

Journal: Current opinion in neurology

Published: August 22, 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

Real-world effectiveness and safety of zilucoplan in patients with anti-AChR myasthenia gravis: A retrospective cohort study in France.

Real-world effectiveness and safety of zilucoplan in patients with anti-AChR myasthenia gravis: A retrospective cohort study in France.

Journal: Journal of neuromuscular diseases

Published: March 29, 2026

Active-NDM: Development of a patient-reported outcome questionnaire to measure the impact of non-dystrophic myotonia on activity of daily living.

Active-NDM: Development of a patient-reported outcome questionnaire to measure the impact of non-dystrophic myotonia on activity of daily living.

Journal: Journal of neuromuscular diseases

Published: February 02, 2026

Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic Amyotrophy.

Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic Amyotrophy.

Journal: European journal of neurology

Published: January 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

French National Protocol for Diagnosis and Care of Calpainopathy (LGMD R1/LGMD D4): consensus guidelines for clinical practice.

French National Protocol for Diagnosis and Care of Calpainopathy (LGMD R1/LGMD D4): consensus guidelines for clinical practice.

Journal: Orphanet journal of rare diseases

Published: December 16, 2025

Multidisciplinary management of Duchenne muscular dystrophy from childhood to adulthood.

Multidisciplinary management of Duchenne muscular dystrophy from childhood to adulthood.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: December 14, 2025

Filnemus Heart-Muscle Day: Improving cardiac management in neuromuscular diseases

Filnemus Heart-Muscle Day: Improving cardiac management in neuromuscular diseases

Journal: Medecine sciences : M/S

Published: November 28, 2025

Real-Life Effectiveness After Switching to Avalglucosidase Alfa in Late-Onset Pompe Disease Patients Worsening on Alglucosidase Alfa Therapy: A French Cohort Study.

Real-Life Effectiveness After Switching to Avalglucosidase Alfa in Late-Onset Pompe Disease Patients Worsening on Alglucosidase Alfa Therapy: A French Cohort Study.

Journal: European journal of neurology

Published: November 23, 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

Phenotype-specific muscle proteomic profiling in titinopathies.

Phenotype-specific muscle proteomic profiling in titinopathies.

Journal: Acta neuropathologica communications

Published: September 12, 2025

Showing 1-12 of 125

Last Updated: 09/26/2026