Vincent Laugel
Strasbourg, France
Last Updated: 09/26/2026
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Found 111 publications
Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.
Journal: Human mutation
Published: January 25, 2026
Gene therapy in Duchenne muscular dystrophy.
Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie
Published: December 14, 2025
Evaluation of the contribution of trio-exome sequencing in selected prenatal indications.
Journal: Frontiers in genetics
Published: December 05, 2025
Accelerating recruitment in clinical trials: A strategic challenge.
Journal: Therapie
Published: November 02, 2025
Accelerating recruitment in clinical trials: A strategic challenge.
Journal: Therapie
Published: November 02, 2025
Safety and Efficacy of Tamoxifen in Patients with Duchenne muscular dystrophy: open Label Extension of TAMDMD Trial.
Journal: Neuromuscular disorders : NMD
Published: October 15, 2025
Comparative Clinical Outcomes of Nusinersen and Gene Therapy in Spinal Muscular Atrophy Type 1.
Journal: JAMA network open
Published: October 08, 2025
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Journal: medRxiv : the preprint server for health sciences
Published: September 15, 2025
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Journal: Nature genetics
Published: September 02, 2025
Cost-Effectiveness and Public Health Impact of Newborn Screening for Spinal Muscular Atrophy in France.
Journal: Applied health economics and health policy
Published: July 25, 2025
Last Updated: 09/26/2026