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Inflammatory Myopathies with Anti-Ku Antibodies
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
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Underappreciated Statin-Induced Myopathic Weakness Causes Disability
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Clinicopath Conf., Colchicine Myoneuropathy
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A 42-year-old man with unilateral leg weakness
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A Child with Delayed Motor Milestones and Ptosis
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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A 52-year-old Woman with Progressive Proximal Weakness
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The Limbic-Girdle Muscular Dystrophies
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
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Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
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Central Core Disease, Clinical Features in 13 Patients
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Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Muscle Fiber-Type Disproportion
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