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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 associated ATPase biochemical blood bulbar carnitine carnitine deficiency carrier cause cells central core disease changes child congenital contractures decreased defect denervation dermatomyositis described diagnosis disorder distal doses Duchenne dystrophy Duchenne muscular dystrophy elevation endplate Engel enzyme exercise test extraocular facioscapulohumeral dystrophy fasciculations fatty acids Figure forearm function genetic glycogen hypokalemic periodic paralysis hypotonia illness increased infantile internal nuclei involved kinase lactate legs levels limb membrane metabolism mild mitochondrial motor neuron disease muscle biopsy muscle fibers Muscle Nerve myasthenia gravis myasthenic myoglobin myoglobinuria myositis myotonia myotonic dystrophy nemaline myopathy 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 suggested symptoms syndrome tissue treatment Type 1 fiber usually walk