A Child with Arthrogryposis
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A Child with Delayed Motor Milestones and Ptosis
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Neurologic Aspects of Inflammatory Bowel Disease
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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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Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
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Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010
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Chronic Limb-Girdle Myasthenia Gravis
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Clinical and Electrophysiologic Improvement in Lambert-Eaton Syndrome with Intravenous Immunoglobulin Therapy
Neurol 42:1422-1423, Bird,S.J., 1992
The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
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Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin E Deficiency
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011
Erroneous Diagnosis Corrected After 28 Years
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Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
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Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
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