Disease: Spine rigid cardiomyopathy
- <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
- 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