Disease: Myopathy with lysis of myofibrils
- Acute myopathy with selective lysis of myosin filaments
- An autopsy case of neonatal lactic acidosis
- Coffee Senna (Senna occidentalis) poisoning in cattle in Brazil
- Congenital myopathies with "diagnostic" pathological features
- Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration
- Disruption of myofibrils during spreading degeneration. I. Increased Ca2+ concentration
- Familial myopathy with probable lysis of myofibrils in type 1 fibers
- Familial myopathy with probable lysis of myofibrils in type I fibers
- Focal myofibrillar disorganization in acute metabolic impairment of somatic musculature
- Hereditary dilated cardiomyopathy in Holstein-Friesian cattle in Japan: association with hereditary myopathy of the diaphragmatic muscles
- Hypotrophic type I muscle fibres with central nuclei, and central myofibrillar lysis preferentially involving type II fibres
- Infantile fibre type disproportion, myofibrillar lysis and cardiomyopathy: a disorder in three unrelated Dutch families
- Morpho- and pathogenesis of muscle injury in the crush syndrome
- Morphologic changes in extraocular muscles of the dystrophic hamster
- Myofibrillar myopathies due to a novel mutation in exon 8 of the LDB3 gene
- Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred
- Ophthalmoplegic myopathy
- The distribution of desmin and titin in normal and dystrophic human muscle