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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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A 52-year-old Woman with Progressive Proximal Weakness
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Glycogen-Storage Disease Type II
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Clinical and Genetic Aspects of Distal Myopathies
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Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
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Bent Spine Syndrome
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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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Inclusion Body Myositis and Myopathies
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
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Benign Familial Disease with Muscle Mounding and Rippling
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Tibial Muscular Dystrophy
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Congenital Muscular Dystrophy
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Quadriceps Myopathy in Two Brothers
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A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
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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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The Oculopharyngeal Syndrome
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Myopathy of the Quadriceps Muscles
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Progressive Camptocormia with Head Drop and Dysphagia
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A 31-year-Old Man with Bilateral Limited Mobility of Joints
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A 36-Year-Old Man With Asymmetric Muscle Weakness
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A 63-Year-Old Woman Presenting with Bilateral Leg Pain
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Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
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