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Congenital Muscular Dystrophy
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Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
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Progressive Camptocormia with Head Drop and Dysphagia
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Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
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Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
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Muscular Dystrophies
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Subacute Paresis in a 28-year-old man with HIV
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 64-year-old Man with Progressive Paraspinal Muscle Weakness
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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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A 51-year-old Woman with Weakness and Stiff Neck
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The Limbic-Girdle Muscular Dystrophies
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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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Diagnosis and Etiology of Congenital Muscular Dystrophy
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Clinicopath Conf., Colchicine Myoneuropathy
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Congenital Muscular Dystrophy:Use of Brain MR Imaging to Predict Merosin Deficiency
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Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
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Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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Investigation of Muscle Disease
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Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
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Late-Onset Mitochondrial Myopathy
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Congenital Myopathies
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Sudden Onset of Profound Weakness in a Toddler
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Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
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