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Chapter 1 THE SYMPTOMS AND SIGNS
Chapter 2 DISEASES OF THE MOTOR NEURONS
Chapter 3 DISEASES OF THE NEUROMUSCULAR JUNCTION
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abnormal acetylcholine receptor activity amyotrophic lateral sclerosis antibody antigens Arch arms associated ATPase biochemical blood bulbar carnitine carnitine deficiency carrier cause cells changes child congenital muscular dystrophy contractures decreased defect denervation dermatomyositis described diagnosis disorder distal doses Duchenne dystrophy Duchenne muscular dystrophy elevation endplate Engel enzyme exercise test facioscapulohumeral dystrophy fasciculations fatty acids Figure forearm function genetic glycogen hypokalemic periodic paralysis hypotonia illness increased infantile internal nuclei involved kinase knee lactate legs levels limb McArdle's disease membrane metabolism mild mitochondrial motor neuron disease muscle biopsy muscle fibers Muscle Nerve myasthenia gravis myasthenic myoglobin myoglobinuria myopathy myositis myotonia myotonic dystrophy Neurol Neurology neuromuscular disease normal noted occur onset oxidative oxygen patients periodic paralysis polymyositis potassium prednisone progressive protein ptosis reaction respiratory response seen serum severe shoulder showed spinal muscular atrophy stain steroids studies symptoms syndrome tissue treatment Type 1 fiber usually walk