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Neuromuscular Disorders : NMD|March 8, 2016
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcomeKarim Wahbi, Frederic A Sebag, Nicolas Lellouche, et al.Genomics, Proteomics & Bioinformatics|October 24, 2025
Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion DisordersLouise Benarroch, Pierre-Yves Boëlle, Hélène Madry, et al.Frontiers in Neurology|October 23, 2019
Novel Phenotypes and Cardiac Involvement Associated With DNA2 Genetic VariantsAriadna González-Del Angel, Michela Bisciglia, Steven Vargas-Cañas, et al.Neurology(R) Neuroimmunology & Neuroinflammation|July 31, 2025
N-Glycan-Dependent Proinflammatory Effects of IgM in Anti-MAG NeuropathyJean Neil, François Fenaille, Arnaud Bruneel, et al.Journal of Neuromuscular Diseases|November 19, 2016
Laminin α2 Deficiency-Related Muscular Dystrophy Mimicking Emery-Dreifuss and Collagen VI related DiseasesIsabelle Nelson, Tanya Stojkovic, Valérie Allamand, et al.Human Molecular Genetics|November 26, 2025
C-terminal extension of HSPB6 in a family with myopathy and cataractJaakko Sarparanta, Per Harald Jonson, Anna Vihola, et al.Neuromuscular Disorders : NMD|May 29, 2016
Relationship between muscle impairments, postural stability, and gait parameters assessed with lower-trunk accelerometry in myotonic dystrophy type 1Damien Bachasson, Amélie Moraux, Gwenn Ollivier, et al.Journal of Neuromuscular Diseases|November 14, 2022
LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMDTanya Stojkovic, Marion Masingue, Corinne Métay, et al.Annals of Clinical and Translational Neurology|April 21, 2020
A new congenital multicore titinopathy associated with fast myosin heavy chain deficiencyAurélien Perrin, Corinne Metay, Marcello Villanova, et al.Plos One|December 2, 2016
Correction: Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMAMohamed-Mounir El Mendili, Timothée Lenglet, Tanya Stojkovic, et al.Pageof 25