• <em>GLB1-</em>Related Disorders
• <em>LAMA2</em> Muscular Dystrophy
• ASC-1 Is a Cell Cycle Regulator Associated with Severe and Mild Forms of Myopathy
• BAG3 mutation in a patient with atypical phenotypes of myofibrillar myopathy and Charcot-Marie-Tooth disease
• BAG3-related myofibrillar myopathy: a further observation with cardiomyopathy at onset in pediatric age
• Clinical aspects of Emery-Dreifuss muscular dystrophy
• Clinical-pathological correlations in three patients with fibrodysplasia ossificans progressiva
• Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy
• Effect of nutritional therapy in Emery-Dreifuss muscular dystrophy: a case report
• Exome sequencing identifies variants in two genes encoding the LIM-proteins NRAP and FHL1 in an Italian patient with BAG3 myofibrillar myopathy
• FHL1-related myopathy may not be classified by reducing bodies in muscle biopsy
• Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
• Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies
• Myofibrillar myopathy caused by a novel FHL1 mutation presenting a mild myopathy with ankle contracture
• Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy - a case report
• SELENON-Related Myopathy Across the Life Span, a Cross-Sectional Study for Preparing Trial Readiness
• Upper Thoracic Spine Synovial Cyst Resulting in Paraplegia Following Transient Hypotension
• Wide Spectrum of Cardiac Phenotype in Myofibrillar Myopathy Associated With a Bcl-2-Associated Athanogene 3 Mutation: A Case Report and Literature Review