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Chapter 1 THE SYMPTOMS AND SIGNS
Chapter 2 DISEASES OF THE MOTOR NEURONS
Chapter 3 PERIPHERAL NEUROPATHIES
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abnormal acid maltase acute amyotrophic lateral sclerosis Arch arms associated attack autosomal dominant axonal BIBLIOGRAPHY bulbar carnitine carriers cause cells central core disease changes child clinical congenital contractures deep tendon reflexes deficiency denervation dermatomyositis diagnosis difficulty distal doses Duchenne Duchenne's dystrophy effect Electromyography Engel enzyme evaluation examination exercise extraocular facial weakness facioscapulohumeral dystrophy fasciculations Figure forearm genetic hand hip weakness hypokalemic periodic paralysis hypotonia illness increased infantile inherited internal nuclei involved knee Laboratory Studies legs membrane metabolic mild motor neuron disease motor unit movement muscle biopsy muscle fibers muscular dystrophy myasthenia gravis myasthenic myelin myoglobinuria myotonia myotonic dystrophy nemaline myopathy Neurology neuromuscular disease normal occur onset pain pathological patients with myasthenia periodic paralysis peripheral nerve peripheral neuropathy polymyositis potassium prednisone progressive protein proximal weakness ptosis respiratory scapuloperoneal seen sensory serum severe shoulder showed spinal muscular atrophy steroids symptoms syndrome treatment Type 1 fiber usually walk