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Multiple Sclerosis Presenting as Lower Motor Neuron Wasting and Weakness of the Distal Upper Extremity
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CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
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Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
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Subacute Progressive Sensorimotor Symptoms
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A 65-year-old man with Asymmetric Weakness and Parethesias
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Chronic and Slowly Progressive Weakness of the Legs and Hands
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Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
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Amyloid Myopathy Presenting with Distal Atrophic Weakness
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Inclusiong Body Myositis Mimicking Motor Neuron Disease
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Distal Hereditary Upper Limb Muscular Atrophy
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Multifocal Motor Neuropathy
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
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Monomelic Amyotrophy
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Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
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Charcot-Marie-Tooth Disease Associated With"Essential Tremor"
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Chronic Spinal Muscular Atrophy in Adults
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