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Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
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"Boule Du Biceps" in Dysferlinopathy
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The Spectrum of Neurologic Disease in the Severe Acute Respiratory Syndrome Coronavirus 2 Pandemic Infection
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A 40-Year-Old Woman Presenting with Distal Leg Weakness
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Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
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Mechanisms, Causes, and Effects of Hypercapnia
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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The Floppy Infant: Evaluation of Hypotonia
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Amyloid Myopathy Presenting with Distal Atrophic Weakness
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Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
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Polymyositis Masquerading as Motor Neuron Disease
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A Novel, Blood-Based Diagnostic Assay for Limb Girdle Muscular Dystrophy 2B and Miyoshi Myopathy
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Inclusiong Body Myositis Mimicking Motor Neuron Disease
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Clinical and Genetic Aspects of Distal Myopathies
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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The Wide Spectrum of Myofibrillar Myopathy Suggests a Multifactorial Etiology and Pathogenesis
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The Muscular Dystrophies
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Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
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Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
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Inclusion Body Myositis:Clinical and Pathological Boundaries
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Pure Motor Hand Weakness
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Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
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Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
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Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Distal Vacuolar Myopathy in Nephropathic Cystinosis
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Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke-Like Episodes (MELAS) :Clinical, Radiological, Pathol & Genetic Observ
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Tibial Muscular Dystrophy
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Molecular Genetics in Neurology
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Chronic Limb-Girdle Myasthenia Gravis
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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