Armelle Magot

Nantes, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 76 publications

Severe dilated cardiomyopathy in females with dystrophinopathy : a case series of nine patients.

Severe dilated cardiomyopathy in females with dystrophinopathy : a case series of nine patients.

Journal: Neuromuscular disorders : NMD

Published: February 20, 2026

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

Electrocardiogram vs Electrophysiological Study and Major Conduction Delays in Myotonic Dystrophy Type 1.

Electrocardiogram vs Electrophysiological Study and Major Conduction Delays in Myotonic Dystrophy Type 1.

Journal: JAMA cardiology

Published: September 24, 2025

Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study.

Limb Girdle Muscular Dystrophy Associated With TRIM32 Variants: A National Cohort Study.

Journal: Muscle & nerve

Published: September 08, 2025

Laminopathies: natural history and risk prediction of heart failure.

Laminopathies: natural history and risk prediction of heart failure.

Journal: European heart journal

Published: June 06, 2025

Causes of Death and Comorbidities in Adult Patients With Late-Onset Pompe Disease: A French Pompe Registry Retrospective Study.

Causes of Death and Comorbidities in Adult Patients With Late-Onset Pompe Disease: A French Pompe Registry Retrospective Study.

Journal: European journal of neurology

Published: May 20, 2025

Etiologic Diagnosis of Neuropathies Based on First-Line Screening of TTR Gene Mutations.

Etiologic Diagnosis of Neuropathies Based on First-Line Screening of TTR Gene Mutations.

Journal: Journal of the peripheral nervous system : JPNS

Published: April 20, 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

Guillain-Barré syndrome in patients with Charcot-Marie-Tooth type 1A disease, probably a non-random association.

Guillain-Barré syndrome in patients with Charcot-Marie-Tooth type 1A disease, probably a non-random association.

Journal: Neurophysiologie clinique = Clinical neurophysiology

Published: February 15, 2025

Spinal muscular atrophy is also a disorder of spermatogenesis.

Spinal muscular atrophy is also a disorder of spermatogenesis.

Journal: Orphanet journal of rare diseases

Published: May 29, 2024

Human MuStem cells are competent to fuse with nonhuman primate myofibers in a clinically relevant transplantation context: A proof-of-concept study.

Human MuStem cells are competent to fuse with nonhuman primate myofibers in a clinically relevant transplantation context: A proof-of-concept study.

Journal: Journal of neuropathology and experimental neurology

Published: May 16, 2024

Showing 1-12 of 76

Last Updated: 09/26/2026