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A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
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A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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Neuropathy, Encephalopathy, Status Epilepticus, and Acute Intermittent Porphyria
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Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
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Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
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A 64-year-old Man with Progressive Paraspinal Muscle Weakness
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Evaluation of a Patient with Spinal Cord Infarction after a Hypotensive Episode
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Paraneoplastic Neurological Syndromes
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
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A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
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Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
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Clinicopath Conf, Dopamine-Responsive-Dystonia Caused by a Mutation in the GCH1 Gene
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Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
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Disease Progression in Sporadic Inclusion Body Myositis: Observations in 78 Patients
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The Muscular Dystrophies
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Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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