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Heterogeneity of Coenzyme Q10 Deficiency
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Neurotoxicity of Commonly Used Antineoplastic Agents
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Neurological Problems in Endocrine Diseases
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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
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A 73-Year-Old Man With Progressive Proximal Muscle Weakness and Binocular Diplopia
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Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
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A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
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Acute Flaccid Myelitis: Cause, Diagnosis, and Management
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Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
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Progressive Proximal Weakness in a 61-Year-Old Man
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Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
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Correlation of Clinicoserologic and Pathologic Classifications of Inflammatory Myopathies
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A Case of Necrotizing Myopathy with Proximal Weakness and Cardiomayopathy
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New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
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Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
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Paraneoplastic Necrotizing Myopathy, Clinical and Pathologic Features
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Acute Myopathy After Liver Transplantation
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Peripheral Neuropathy Secondary to Docetaxel (Taxotere)
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Peripheral Neurotoxicity Induced by Docetaxel
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Acute Focal Neuropathy in Male Weight Lifters
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Motor Neuropathy Due to Docetaxel and Paclitaxel
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Neurologic Aspects of Inflammatory Bowel Disease
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Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
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Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
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Acromegaly:Clinical and Biochemical Features in 500 Patients
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Sudden Onset of Profound Weakness in a Toddler
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Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
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Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
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Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
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Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
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Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
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The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
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Central Core Disease, Clinical Features in 13 Patients
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